Statistician Salary in India - PayScale

Recruitment of XII 12th Selection Vacancy posts by 9 SSC RegionsOnline applications in the prescribed format are invited from eligible candidates for the following various 2049 Group-B and Group-C Selection Sarkari Naukri Vacancy Posts by 9 Regional Offices of Staff Selection Selection (SSC) situated at Kolkata (Eastern Region), Guwahati (North Eastern Region), Raipur (Madhya Pradesh Region), New Delhi (Northern Region),  Mumbai (Western Region), Allahabad (Central Region), Bangalore (Karnataka Kerala Region), Chandigarh (North Western Region,),  Chennai (Southern Region) for XII (12th) edition of combined selection posts vacancy recruitment 2024. (Advt. No. Phase-XII/2024/Selection Posts). SarkarinaukriBlog.com (adsbygoogle = window.adsbygoogle || []).push({});Selection Posts 12 12th Recruitment 2024 by SSC - Table of ContentSSC XII 12th Selection Posts 2024 - VacanciesApplication FeeSSC XII 12th Selection Posts Vacancy 2024 Examination DetailHow to Apply for SSC XII 12th Section Posts Vacancy 2024?Detailed information and Application SubmissionSSC 12 XII Selection Posts Recruitment 2024 - VacanciesThe 12th Selection posts for the year 2024 are listed herein alphabetically ordered. Some posts are shown here combined vacancies. The recruitment for these XIIth selection posts is to be done by various regional offices of SSC only. Please view the detailed advertisement for better information. (adsbygoogle = window.adsbygoogle || []).push({});The vacancies have been advertised  for the year 2024 in the 12th Selection posts by the Staff Selection Commission (SSC) as per the Indents submitted by the respective Indenting Departments/ Offices. There may be withdrawal/ alteration of the vacancies by the Indenting Departments/ Offices. Candidates who wish to apply for more than one post should apply separately for each post irrespective of the education level of the post.12th Selection Posts: 2049 vacancies of Library Attendant, Medical Attendant, Nursing Officer, Pharmacist (Allopathic), Fieldman, Deputy Ranger, Junior Technical Assistant, Technical Assistant, Senior Technical Assistant, Accountant, Assistant Plant Protection Officer, Senior Scientific Assistant, Foreman, Laboratory Attendant, Junior Engineer, Driller-cum-Mechanic, Library and Information Assistant, Girl Cadet Instructor, Upper Division Clerk (UDC), Data Entry Operator, Junior Computer, Stockman, Driver-cum-Mechanic, Canteen Attendant, Assistant Communication Officer, Supervisor, Assistant Central Intelligence Officer (ACIO), Junior Physiotherapist, Data Processing Assistant, Civil Motor Driver, Khansama Chowkidar, Sub-Inspector, Senior Translator, Rehabilitation Counsellor, Staff Car Driver, Laboratory Assistant, Evaluator, Supervisor, Library and Information Assistant, Store Keeper, Research Investigator, Carpenter-cum-Artist, Court Clerk, Clerk, Senior Geographer, Field Worker, Senior Educational Assistant, Junior Translator, Draftsman, Lower Division Clerk (LDC), Education Assistant, Senior Educational Assistant, Sign Board Painter, Research Assistant, Documentation Assistant, Caretaker, Wildlife Inspector, Senior Photographer, Telephone Operator, Assistant Archeologist, Accounts Clerk, Carpenter cum artist, Field Worker, Dispatch Rider, Garden Superintendent, Copyholder, Deputy Ranger, Manager-cum-Accountant, Technician, Insect Collector, Textile Designer, Statistician-cum-Medical Record Librarian, Mechanic, Senior Draughtsman, Girl Cadet Instructor, Accounts Clerk, Proof Reader, Office Superintendent, Proof Reader, Weaver, Block cum Screen Painter, Lettering Artist, Security Man, Mud Plaster, Urdu Translator, Manager, vocational Instructor, Multi Tasking Staff (MTS) etc. in 9 Regions of SSCAge: 18-25, 18-27, 18-30 years as of 01/01/2024Pay Level: 7th CPCPay Level-1 ₹18000-56900Pay Level-2 ₹19900-63200Pay Level-3 ₹21700-69100Pay Level-4 ₹25500-81100Pay Level-5 ₹29200-92300Pay Level-6 ₹35400-112400Pay Level-7 ₹44900-142400 (adsbygoogle = window.adsbygoogle || []).push({});Application FeeThe application fee for the SSC 12th Selection Posts is ₹100/- to be paid online through BHIM UPI, Net Banking, by using Visa, Mastercard, Maestro, RuPay Credit or Debit cards or in SBI Branches by generating SBI Challan. No fee for SC/ ST/ PH/ Ex-Servicemen and Women candidates.SSC XII Selection Posts 2024 Examination PatternThere will be a Computer Based Mode of Examinations consisting of Objective/Multiple Choice Questions for SSC 12th Selection Vacancy posts in 6-8 May 2024 tentatively, separately for each post with minimum Educational Qualification of Matriculation, Higher Secondary, and Graduation.The computer-based SSC 12th Selection Posts 2024 Vacancy Exam will be held in the month of 6-8 May 2024 tentatively at various test centers across India. The total duration of the exam is 60 minutes (1 hour) and the total marks of the exam are 200. There will be negative marking of 0.50 marks for each wrong answer.General Intelligence - 25 questions / 50 marksEnglish Language (Basic Knowledge) - 25 questions / 50 marksQuantitative Aptitude (Basic Arithmetic Skill) - 25 questions / 50 marksGeneral Awareness  - 25 questions / 50 marksView - All Guidebooks for Government Job Competitive Recruitment Exams. How to Apply for SSC XII 12th Selection Post Recruitment 2024? Suitable and desirable candidates should apply online in the prescribed format at the SSC Recruitment website at https://ssc.gov.in from 26/02/2024 to 18/03/2024 only for SSC XII 12th Selection Posts Vacancy Recruitment 2024. Window for Application Form Correction is from 22/03/2024 to 24/03/2024.The SSC Selection Posts are consist ofGovernment Jobs for 10th PassGovernment Jobs for 12th PassGovernment Jobs for Graduate level pass View - Guidebooks for Government Job Competitive Recruitment Exams. Details and Online Submission of Application For further details for all these 12th selection posts 2024 by 9 Regional Offices of Staff Selection Commission SSC are available at http://www.sscnr.net.in for Northern Region at Delhi,  http://www.ssc-cr.org for Central Region at Allahabad, http://www.sscer.org for Eastern Region at Kolkata, http://www.sscwr.net for Western Region at Mumbai, http://www.sscsr.gov.in for Southern Region at Chennai, http://www.sscnwr.org for North Western Region at Chandigarh, http://www.ssckkr.kar.nic.in for Kerala Karnataka Region at Bengaluru,  http://www.sscner.org.in for North Eastern Region at Guwahati, http://www.sscmpr.org for MP Chhattisgarh Region at Raipur, please see details of every region for every post, etc. by visiting the website of  that region, and apply online at https://ssc.gov.in (adsbygoogle = window.adsbygoogle || []).push({}); { "@context": "https://schema.org/", "@type": "JobPosting", "title": "SSC XIIth 12th Selection Posts Vacancy Recruitment 2024", "description": "Online applications are invited from eligible candidates for the following various Selection Sarkari Naukri Vacancy Posts by Staff Selection Selection (SSC) 9 Regional Offices under XIth 12th Selection Posts Vacancies Recruitment 2024. To know more detail please click on the above blue Button \"Apply On SarkariNaukriBlog.com\".", "identifier": { "@type": "PropertyValue", "name": "SarkariNaukriBlog", "value": "Phase-XII/2023/Selection Posts" }, "datePosted": "2024-02-26T10:30", "validThrough": "2024-03-18T23:00", "employmentType": "Full_Time", "hiringOrganization": { "@type": "Organization", "name": "Staff Selection Commission (SSC)", "sameAs": "https://ssc.gov.in", "logo": "https://ssc.gov.in/assets/sscLogo.webp" }, "jobLocation": { "@type": "Place", "address": { "@type": "PostalAddress", "streetAddress": "Block No-12, CGO Complex, Lodhi Road", "addressLocality": "New Delhi", "addressRegion": "Delhi", "postalCode": "110003", "addressCountry": "India" } }, "baseSalary": { "@type": "MonetaryAmount", "currency": "INR", "value": { "@type": "QuantitativeValue", "value": 44900, "unitText": "MONTH" } }}Compiled by Sarkari-Naukrifor blog https://www.sarkarinaukriblog.com/for providing Government Jobs available in India. .  Other Blogs are https://www.HindiDiary.com and Friendly blog is https://www.rojgarjob.com At Facebook at https://www.facebook.com/SarkariNaukriBlogSpot and Twitter at https://twitter.com/sarkarijob (@SarkariJob)

Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come together to advance the state of clinical development.Who Are You?An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I:IV clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same.Sponsor:dedicated:Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, youll be at the heart of our clients innovation. As a Principal Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.Position Overview:Our Principal Biostatisticians provide statistical and development support and influence for the associated clients trials providing expertise into processes, clinical development plans, concept sheets and protocols, as well as potentially providing oversight of work supported by other vendors. You will formulate integrated analytical approach to mine data sources, employ statistical methods, machine learning and deep learning algorithms to discover actionable insights and automate process for reducing effort and time for repeated use.As Principal Biostatistician, adapt at utilizing advanced statistical methods, you will support or lead one or more Phase I:IV clinical studies. Experience of primarily leading medium complexity clinical trials (starting from Design to Archival experience) and supporting some project:level activities.Summary of Job Responsibilities:- Demonstrated experience in project leadership: project planning, interaction with different stakeholders, scientific supervision of statisticians.- Scientific leader: excellent knowledge and experience in survival analysis, and linear and generalized linear models.- Capacity to interface effectively with clinicians and statistical programmers.- Capacity to work independently.- Capacity to quickly read late development protocols, understand the statistical methodology, and apply it to clinical data.- Knowledge and practice of CDISC SDTM and ADaM data standards.- Ability to work in compliance with the company Analysis and Reporting SOPs and project data standards. Able to re:in force the compliance.- Fast learner, team:oriented, able to work independently.- Knowledge of SAS programming SAS/STAT SAS/BASE, SAS macro language. Experience with SAS on PC and UNIX platforms.Qualifications and Experience:- MSc or Ph.D. in Statistics.- 8:10 years of relevant clinical trial biostatistics support in design, analysis, and interpretation. Proven experience of work with clinical trialdata in support of safety and efficacy analysis- Ability to read, write and speak fluently in English.- CDISC knowledge is required.Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have::Master's degree in statistics or a related discipline. Ph.D. strongly desired.:9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.:Ability to work independently, demonstrate initiative and flexibility through effe

Responsibilities: Work closely with customers and WWT business, engineering, and technology teams. Work with large, complex data sets. Solve difficult, non-routine analysis problems, applying advanced analytical methods as needed. Conduct end-to-end analysis that includes data gathering and requirements specification, processing, analysis, ongoing deliverables, and presentations. Work on advanced analytics areas like deep learning and complex statistical data analysis Interact with clients including in-person meetings, towards making business recommendations with effective presentations of findings, including visual displays of quantitative information. Develop analysis, forecasting and optimization methods/models to provide the business solution to the clients. Research and develop internal capabilities to enhance the skill sets on latest data science developments, work towards producing innovative solutions to the existing challenges. Perform quality control of deliverables. Provide thought leadership in algorithmic and process innovations and contribute to creativity in solving unconventional problems. Qualifications : Education Preferably a Ph.D. but also open to master's or bachelor's degree in a quantitative discipline (e.g., statistics, computer science, economics, mathematics, physics, electrical engineering, industrial engineering, or other STEM fields) Work Experience 4-6years of relevant work experience in data analysis or related field. (e.g., as a statistician / data scientist/ data engineer). D. Research and post-doctoral experience also counts . Specialized Knowledge, Skills, and Abilities We do not need an exceptional IQ of 160. All we need is curiosity, humility, and openness to learn. In other words, we just need a Beginner's Mind, even if you have decades of professional experience. Analysis Experience with writing SQL queries, performing basic conversion and transformations (formatting date string), and obtaining statistical summaries by using windowing functions. Experience with usage of R/RStudio, Python, JupyterNotebook Experience with version control tool like Git Strong experience with Excel and PowerPoint to present results. Ability to write scripts to automate ETL tasks . Experience in AI / Deep Learning for text/image/video analytics preferred. Experience in Cloud Computing and data streaming preferred. Problem Solving Ability to run standard model algorithms in R and Python, to perform: classification/regression, clustering, basic text analytics, image recognition, etc. g., run a classification problem using random forest, and obtain the variable importance, produce performance metrics/KPIs; run a k-means clustering problem, produce a KPI to quantify the goodness of clusters. Demonstrated skills in selecting the right statistical tools given a data analysis problem . Experience with charting tools & knowledge of the proper charting tool to use, whether Excel or Tableau. For instance, when to use box-and-whiskers plot, when to use waterfall. Ability to zoom-in to smaller data sets in Tableau or display subcategories. Capable of running multiple scenarios and pick up the optimal solution. Capable of understanding advanced mathematical or physical explanations, to implement or execute the requested tasks. Fourier Transform, Power Spectral Density, Monte Carlo simulation, etc. Actively participates and contributes to brain -storming session . Can work seamlessly with people from other disciplines: IT engineers, client SMEs, business consultants. Experience articulating business questions and using mathematical techniques to arrive at an answer using available data. Experience translating analysis results into business recommendations. Team & Business Skills Consistently improves communication skills, both verbally and in written materials Demonstrated creativity in problem solving. Demonstrated leadership and self-direction. Demonstrated willingness to both teach others and learn new techniques. Flexibility in task switching. For instance, when there are urgent requests or change of projects, can accommodate the changes without protesting . Mindful of iterations and quality check in a smaller team, before presenting results to larger audience Raises critical issues when detected. The well-being of WWT employees is essential. So, when it comes to our benefits package, WWT has one of the best. We offer the following benefits to all full-time employees: Health and Wellbeing: Heath, Dental, and Vision Care, Onsite Health Centers, Employee Assistance Program, Wellness program Financial Benefits: Competitive pay, Profit Sharing, 401k Plan with Company Matching, Life and Disability Insurance, Tuition Reimbursement Paid Time Off: PTO & Holidays, Parental Leave, Sick Leave, Military Leave, Bereavement Additional Perks: Nursing Mothers Benefits, Voluntary Legal, Pet Insurance, Employee Discount Program Salary: . Date posted: 03/25/2024 07:12 AM

Job Title: Lead Statistical Programmer Department: Biostatistics Job Level :7 Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future:ready environment and support your colleagues and stakeholders by challenging the status:quo in a friendly and open:minded way? If so, there is a job opportunity waiting for you as our new Lead Statistician. At NovoNordisk, we will challenge you to do the best work of your life. Apply Now. About the Department:Biostatistics department was established in October 2010. The team has a good blend of experience and fresh perspective and comprises experienced statisticians and programmers, who form the core of the team. The main purpose and objective is to ensure high quality in preparing and conducting statistical analysis in accordance with the project milestones and provide statistical support and expertise to all clinical development activities within Novo Nordisk. The Position: The Lead Statistical Programmer will be responsible for statistical programming and reviewing SAS/R programs in the designated clinical trial. Will also be responsible for sharing best practices and adhering to project and other programming standards, as well as guiding and mentoring less experienced statistical programmers. Additionally, the Lead Statistical Programmer is accountable for::Provide programming input to the setup of the trial, including but not limited to the CRF, Trial Validation Plan and Data Flow Plan. :Responsible for creating and gathering input to the Specification ADRG for the clinical trial, and ensuring it is aligned with Project ADRG. Ensure that mock TFLs are created and reviewed by stakeholders. Programming/ review of ADaM, Safety and Efficacy TFLs according to specifications for Clinical Study Report, ISS/ISE etc.:Ensure Trial execution and coordination within the trial statistics team.:Responsible for the programming input to Risk Management Plan, Investigators Brochure, DSUR /PSUR and regulatory submission documents:To work closely with trial squad, take initiative, and help with methodological or technically challenging tasks where innovation is essential. Serve as point of contact for programmers from the functional suppliers regarding the programming need.Qualifications:Bachelors or Masters in life sciences or natural sciences or Engineering or equivalent qualifications.:7 + Years of experience in working as a statistical programmer within the pharmaceutical industry.:Experience with SAS programming, ADAM, CDISC (Clinical Data Interchange Standards Consortium), TLF (Technical loss factor), R Programming; expertise of reporting clinical trials, including handling, analysing, and reporting statistical data.:Thorough experience of programme validation and documentation.:Working Knowledge of advanced programming, data models, and clinical database technologies.:Solid understanding of drug development.:Excellent written and spoken English.:Analytical and result oriented.:Good team player with communication and stakeholder management skills.Working at Novo NordiskAt Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world. Since the company was founded in Denmark more than 100 years ago, we have been translating the unmet medical needs of people living with serious chronic diseases into innovative medicines and delivery. Our focus is on these diseases, which affect hundreds of millions of people and are amo

Department: Biostatistics Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future:ready environment and support your colleagues and stakeholders by challenging the status:quo in a friendly and open:minded way? If so, there is a job opportunity waiting for you as our new Senior Statistician. At NovoNordisk, we will challenge you to do the best work of your life. Apply Now. About the Department:Biostatistics department was established in October 2010. The team has a good blend of experience and fresh perspective and comprises experienced statisticians and programmers, who form the core of the team. The main purpose and objective is to ensure high quality in preparing and conducting statistical analysis in accordance with the project milestones and provide statistical support and expertise to all clinical development activities within Novo Nordisk. The Position:The Senior Statistical Programmer will be responsible for statistical programming and reviewing SAS/R programs in the designated clinical trial. Will also be responsible for sharing best practices and adhering to project and other programming standards, as well as guiding and mentoring less experienced statistical programmers. Additionally, the Senior Statistical Programmer is accountable for::Provide programming input to the setup of the trial, including but not limited to the CRF, Trial Validation Plan and Data Flow Plan. :Responsible for creating and gathering input to the Specification ADRG for the clinical trial, and ensuring it is aligned with Project ADRG. Ensure that mock TFLs are created and reviewed by stakeholders. Programming/ review of ADaM, Safety and Efficacy TFLs according to specifications for Clinical Study Report, ISS/ISE etc.:Ensure Trial execution and coordination within the trial statistics team.:Responsible for the programming input to Risk Management Plan, Investigators Brochure, DSUR /PSUR and regulatory submission documents:To work closely with trial squad, take initiative, and help with methodological or technically challenging tasks where innovation is essential. Serve as point of contact for programmers from the functional suppliers regarding the programming need.Qualifications:Bachelors or Masters in life sciences or natural sciences or Engineering or equivalent qualifications.:5 :8 Years of experience in working as a statistical programmer within the pharmaceutical industry.:Experience with SAS programming, ADAM, CDISC (Clinical Data Interchange Standards Consortium), TLF (Technical loss factor), R Programming; expertise of reporting clinical trials, including handling, analysing, and reporting statistical data.:Thorough experience of programme validation and documentation.:Working Knowledge of advanced programming, data models, and clinical database technologies.:Solid understanding of drug development.:Excellent written and spoken English.:Analytical and result oriented.:Good team player with communication and stakeholder management skills.Working at Novo NordiskAt Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world. Since the company was founded in Denmark more than 100 years ago, we have been translating the unmet medical needs of people living with serious chronic diseases into innovative medicines and delivery. Our focus is on these diseases, which affect hundreds of millions of people and are among the most urgent global h

Job Title: Senior Statistician Department: Biostatistics Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future:ready environment and support your colleagues and stakeholders by challenging the status:quo in a friendly and open:minded way? If so, there is a job opportunity waiting for you as our new Senior Statistician. At NovoNordisk, we will challenge you to do the best work of your life. Apply Now. About the Department:Biostatistics department was established in October 2010. The team has a good blend of experience and fresh perspective and comprises experienced statisticians and programmers, who form the core of the team. The main purpose and objective is to ensure high quality in preparing and conducting statistical analysis in accordance with the project milestones and provide statistical support and expertise to all clinical development activities within Novo Nordisk. The Position: The Senior Statistician will be responsible for planning, managing and execution of statistical deliverables in clinical trial and non:trial activities in the project. Providing statistical input to authority required documents or meetings and responsible for ensuring that clinical trial and non:trial tasks are aligned with the project specifications.Additionally, the Senior Statistician is accountable for::Developing statistical design while the protocol Outline and Protocol are being developed, including calculating sample size. Create statistical analysis plan. Provide statistical input to trial:related documents, including but not limited to the Clinical Study Report, mock TFL and blinding plan. Analyze trial findings and present the findings to senior management. At all times during the trial life cycle, make sure the inspection readiness documentation is updated.:Ensure that relevant statistical documentation is made available for public disclosure such as ClinicalTrials.gov and EudraCT. Contribute statistical information to regulatory documents such as Risk Management Plan, Investigational Brochure, and DSUR/PSUR. Contribute statistical information to the creation of submission:related documents, such as ISS/ ISE. Contribute statistical input to the clinical development programs preparation and negotiation at meetings with regulatory authorities, including FDA.:Provide statistical input to clinical trial Specification ADRG and project ADRG. Ensure that statistical analysis and output are programmed and reviewed in accordance with specifications.:Responsibilities of an International Project Statistician include delivering results and ensuring understanding among colleagues relevant to problem:solving. Lead project teams to completion of milestones and objectives. :Prioritize, plan, manage, and carry out Clinical Trials and submissions within the scope of the project. Mentor and develop project area successors. Fully responsible for the projects statistical methodology and deliverables. Qualifications::Minimum 4 plus years of experience working as a statistician within the pharmaceutical industry / PhD in Statistics with less experience/ Masters in statistics (or equivalent) from premier institutes with lesser experience. :Experience with a broad range of statistical tasks. In:depth knowledge of biostatistical methods.:Extensive experience with practical applications of biostatistical methodology.:Broad experience with statistical software and IT and in:depth experience with at least one statistical software package.:Good knowledge of GCP and statistical guidelines within drug development.:Regular experience with communication of statistical issues and presentations.:Some understanding of the pharmaceutical industry, with a focus on how to deliver on own goals.:Solid unde

Bank of India Specialist Officer Vacancy Recruitment 2024Bank of India (BoI), a Public Sector Bank recruits Specialist Officers in various steams/disciplines at various levels under Recruitment Project No. 2023-24/1 and invites online applications in the prescribed format from Indian Citizens for Recruitment of the following various 143 Specialist  Officers for its various offices across India on a regular basis for the year 2024. (Advertisement No. 2023-24/1) (adsbygoogle = window.adsbygoogle || []).push({}); The Bank of India has come up with the vacancy recruitment notification after 2 years for Specialist Officers posts. SarkariNaukriBlog dot com BoI Specialist Officer Recruitment 2023-24/1 VacanciesCredit Officers: 25 vacancies (UR-13, EWS-02, OBC-06, SC-03, ST-01) (PWD-01), Pay Scale: Middle Management Grade Scale-II (MMGS-II) Scale ₹48170-69810/-, Age: 23-35 yearsChief Manager -Economist: 01 vacancies (UR-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-45 yearsChief Manager - IT – DatabaseAdministrator: 02 vacancies (UR-01, OBC-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-40 yearsChief Manager - IT – CloudOperation: 01 vacancies (UR-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-40 yearsChief Manager - IT – Manager: 01 vacancies (UR-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-40 yearsChief Manager - IT – System: 01 vacancies (UR-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-40 yearsChief Manager - IT – Infra: 01 vacancies (UR-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-40 yearsChief Manager - IT – Information Security: 01 vacancies (OBC-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 28-40 yearsChief Manager - IT – Marketing(Chief WealthManager): 01 vacancies (UR-01), Pay Scale: Senior Management Grade Scale-IV (SMGS-IV) Scale ₹76010-89890/-, Age: 32-40 yearsLaw Officers: 31 vacancies (UR-13, EWS-03, OBC-08, SC-04, ST-03) (PWD-02), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 25-35 yearsData Scientist: 02 vacancies (UR-01, SC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsML Ops FullStack Developer: 02 vacancies (UR-01, EWS-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsDatabaseAdministrator: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsData QualityDeveloper: 02 vacancies (UR-01, SC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsDataGovernanceExpert: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsPlatformEngineeringExpert: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsLinuxAdministrator: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsOracle ExadataAdministrator: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager- IT: 04 vacancies (UR-01, OBC-01, SC-01, ST-01) (PWD-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - DataAnalyst: 04 vacancies (UR-01, OBC-01, SC-01, ST-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - Database: 03 vacancies (UR-01, OBC-01, SC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - CloudOperation: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - NetworkSecurity/Operation: 03 vacancies (UR-01, EWS-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - System(Windows/Solaris/RHEL): 04 vacancies (UR-01, EWS-01, OBC-01, SC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - Infra: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - End PointSecurityManager forToolManagement: 01 vacancies (SC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - SecurityAnalyst: 04 vacancies (UR-01, EWS-01, OBC-01, SC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - GRC (Risk& Control): 01 vacancies (UR-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - Fintech: 05 vacancies (UR-01, EWS-01, OBC-01, SC-01, ST-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsSenior Manager - IT - Statistician: 02 vacancies (UR-01, OBC-01), Pay Scale: MMGS-III Scale ₹63840-78230/-, Age: 28-37 yearsLaw Officers: 25 vacancies (UR-09,  EWS-02, OBC-05, SC-07, ST-02) (PWD-01), Pay Scale: Middle Management Grade Scale-II (MMGS-II) Scale ₹48170-69810/-, Age: 25-32 yearsEconomist: 01 vacancies (UR-01), Pay Scale: Middle Management Grade Scale-II (MMGS-II) Scale ₹48170-69810/-, Age: 21-35 yearsTechnicalAnalyst : 01 vacancies (UR-01), Pay Scale: Middle Management Grade Scale-II (MMGS-II) Scale ₹48170-69810/-, Age: 21-35 years (adsbygoogle = window.adsbygoogle || []).push({});Application Fee An application fee of ₹850/- (₹175/- for SC/ST/PWD candidates) to be deposited online by using only Master/ Visa/ RuPay Credit cards, Debitcards, Internet Banking, Cash Cards/Mobile Wallets, QR or UPI. View - All Open Job Vacancies in Public Sector Undertakings Selection Procedure Selection for Specialist Officers in BoI for Recruitment 2023-24/1 will be done through an online test and/or GD and/or personal interview, depending on thenumber of applicants/eligible candidates. Sl. No. Name of the Tests Maximum Marks Duration 1. English Language 25 30 Minutes 2. Professional Knowledge relevant to the post 100 60 Minutes 3. General Awareness with special reference to Banking Industry 25 30 Minutes There will be a penalty for wrong answers marked in the Objective Tests. For each question forwhich a wrong answer has been given by the candidate, a one fourth of the marks assigned to that question will be deducted as a penalty to arrive at a corrected score Candidates securing the minimum qualifying marks stipulated forOnline Tests and ranking sufficiently high in the order of merit shall be called for a Personalinterview and/or GDView - All Open Job Vacancies in Government Banks How to Apply for BoI Specialist Officer Vacancy 2023-24/1?Suitable and desirable candidates should Apply Online in the prescribed format only at the Bank of India website from 27/03/2024 to 10/04/2024 for Specialist Officer Recruitment in Bank of India 2023-24/1.View - All Officer vacancies available right nowDetails and Online submission of applicationKindly visit https://bankofindia.co.in/career/recruitment-notice for detailed information and a link to the online submission of the online application for Security Officer Recruitment in Bank of India 2023-24/1. 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To know more detail please click on the above Blue Button \"Apply On SarkariNaukriBlog.com\".", "identifier": { "@type": "PropertyValue", "name": "SarkariNaukriBlog", "value": "2023-24/1" }, "datePosted": "2024-03-27T10:30", "validThrough": "2024-04-10T23:59", "employmentType": "Full_Time", "hiringOrganization": { "@type": "Organization", "name": "Bank of India (BoI)", "sameAs": "https://bankofindia.co.in", "logo": "https://lh4.ggpht.com/governmentjob/SAR54dYGFrI/AAAAAAAAA8E/gRYo0jaxYzQ/BankOfIndia_thumb%5B2%5D.jpg?imgmax=800" }, "jobLocation": { "@type": "Place", "address": { "@type": "PostalAddress", "streetAddress": "Star House, Plot C-5, “G” Block, Bandra-Kurla Complex,", "addressLocality": "Bandra (East), Mumbai", "addressRegion": "Maharashtra", "postalCode": "400051", "addressCountry": "India" } }, "baseSalary": { "@type": "MonetaryAmount", "currency": "INR", "value": { "@type": "QuantitativeValue", "value": 70000, "unitText": "MONTH" } }}Compiled by Sarkari-Naukrifor blog https://www.sarkarinaukriblog.com/for providing Government Jobs available in India. .  Other Blogs are https://www.HindiDiary.com and Friendly blog is https://www.rojgarjob.com At Facebook at https://www.facebook.com/SarkariNaukriBlogSpot and Twitter at https://twitter.com/sarkarijob (@SarkariJob)

Department: SDTM Programming and SubmissionDoes your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can:do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment.About the departmentBangalore Global Development, Global Business Service (GBS), SDTM Programming and Submission team was established in April 2016 and became a separate department in July 2021. The team has a good blend of experience and fresh perspective and comprises experienced SDTM Subject Matter and Submission experts, who form the core of the team. The main purpose and objective are to ensure high:quality compliant submission:ready SDTM packages in close collaboration with our stakeholders across the clinical landscape, for all clinical trials within Novo Nordisk.The PositionA Senior SDTM Programmer will be responsible for ensuring compliance with Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), Good Documentation Practice (GDP), and Good Programming Practice (GPP) and promote the exchange of knowledge within the organization and externally via participation in meetings/conferences. The Senior SDTM Programmer is recognized as responsible for supporting end users and must act independently, following the strategic objectives of the standards governance bodies and the company in general. The Senior SDTM Programmer will be responsible for assisting in solving methodological or technical demanding tasks where innovation is a key element.Generate SDTM datasets and perform QC. Create and maintain Study Data Reviewer's Guide (SDRG). Prepare contents for the External Committee package based on trial requirements and engage with Safety Surveillance/external statisticians.:Responsible for finalizing Study Data Tabulation Model (SDTM) deliverables and to review of eCRFs, special attention should be given to non:standard modules, regarding the impact on SDTM.:Perform custom programming as required and validate according to relevant SOP.:Run Pinnacle 21 checks and resolve issues by coordinating with the Trial squad. Ensure compliance with the Novo Nordisk SDTM Implementation Guide (NN SDTMIG).:Responsible for reviewing and providing inputs to data collection requirements in relation to but not limited to Protocol, Flow chart, electronic CRFs (eCRF), External Specifications, and SDTM Domains.:Prepare and review metadata specification (as relevant) and aCRF. Submit requests to Standards Teams to either deviate from an existing standard or use a trial:specific element in alignment with the Lead SDTM Programmer.Qualifications:Bachelors or Master in life sciences, natural sciences, pharmacy, veterinary science, engineering, clinical information management, computer science or equivalent qualifications.:Minimum 4:6 years of experience in the Life Sciences industry and preferably 4 years within Clinical Data Management and with hands:on experience in Clinical Data Interchange Standards Consortium (CDISC) SDTM.:Excellent communication skills.:Expert knowledge on end:to:end clinical data management activities.:Experience with collaboration across regional borders.:Experience with mentoring and presentations.:Participation in conferences/workshops.:Demonstrated experience with project management.:Ability to work in a diverse multi:cultural environment.:Good knowledge of GxP and other guidelines within drug development.Working at Novo NordiskAt Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions

The Senior Statistical Programmer will work directly with the stakeholders to lead and contribute to statistical programming projects and to ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements. The Senior Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets and will ensure audit readiness for all tasks. They will provide mentoring and training to statistical programming staff members and may lead or contribute to the design of new statistical programming processes or optimization of existing ones.JOB RESPONSIBILITIES: :Lead statistical programming activities for assigned projects, which will include projects expected to be submitted to regulatory authorities and may include pooling projects (ISS/ISE). :Co:ordinate activities of all programmers assigned to the project, ensuring high quality, respecting project timelines and adherence to the budget. :Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of project requirements, scope of work and timelines.:Provide relevant training and mentorship to staff and project teams on SAS techniques and clinical trial data with respect to CDISC standards and other regulatory requirements.:Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results. :Ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements, for instance: :clinical study reporting, e.g. ICH E3,:electronic records handling, e.g. Chapter 21 of the US Code of Federal Regulation : Part 11, :electronic submission of clinical data to agencies, e.g. e:CTD guidance and CDISC SDTM and ADaM standards.:Understand and follow all relevant standard operating procedures (SOPs).:Keep abreast of current and new statistical programming techniques and other applicable technical advancements while assisting in their implementation. :Maintain up:to:date knowledge of programming software (e.g. SAS, R, Python) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings.:Occasionally, lead, or contribute to, the design of new statistical programming processes or optimization of existing ones to reach the best productivity, to ensure the best quality of the statistical outputs, and to reach the best customer satisfaction (internally and externally) with flexibility, reliability and responsiveness.QUALIFICATIONS: Education: BSc or equivalent with research experience, and/or MS (in a numerate discipline preferably in Statistics, Computer Science, or Mathematics). Master's Degree preferred.Experience: :6 years of experience in biostatistics or statistical programming activities in the Pharmaceutical/Biotechnology industry in clinical development with good knowledge of CDISC ADaM and SDTM, ICH Statistical and Clinical Report Guidelines.:Experience as a lead statistical programmer working with global cross functional teams is required.Skills: :Fluent in English,:Proficient in SAS,:Project management, organizational skills, ability to manage competing priorities, and flexibility to change.:Good understanding of drug development process, including knowledge of interfaces and interdependencies with other functions.:Good time management and interpersonal skills,:Written/verbal communication and presentation skills are needed along with the ability to establish and maintain effective working relationships with coworkers, managers and clients.LI:PJ1