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- 1. Develop documents e.g. Clinical Trial Protocol (CTP) Trial Statistical Analysis Plan (TSAP) Randomization specifications & initiate randomization scheme creation Participate in the development of Integrated Quality and Risk Management (IQRM) plan and MQRP 2....SuggestedInterim rolePunea month ago
- ...for you. Responsibilities Contribute to clinical development plan preparation; Review of study protocol and preparation of statistical methodologies; Development of detailed Medpace Data Analysis Plan for assigned projects; Programming of study analysis,...SuggestedFull timeContract workLocal areaWork from homeHybrid workFlexible hoursPune6 days ago
- ...At Cytel, we believe in empowering our employees for success through consistent training, development, and support. As a Principal Statistical Programmer , you'll be fully embedded within one of our global pharmaceutical clients, a company at the forefront of patient...SuggestedPunea month ago
- ...Fortrea is transforming drug and device development for partners and patients across the globe. Perform the role of the Lead Statistical Programmer. Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation,...SuggestedContract workPunea month ago
- Description Statistical Programmer – L2 Job Summary: Statistical Programmer reports to Principal Statistical programmer 3/Lead, Statistical... ...clinical data and domain ●Follow Client Processes and SOPs ●Assist senior team members in quality control processes ●Assist senior...SuggestedPunea month ago
- ...appropriate stats software, o interpretation of results. o Takes statistical responsibility for one or more standard experiments. o Develops... ...the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of...SuggestedFull timeContract work
- ...Responsibilities • Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR... ...inspection readiness. • Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of...SuggestedFull timeContract work
- ...committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Principal Biostatistician- Clinical TrialsSuggestedFull timeContract work
- Pr Statistical Programmer(SDTM+ ADAM +TLF) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to... ...toward consensus. • Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of...SuggestedFull timeContract work
- Principal Statistical Programmer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate... ...provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the...SuggestedFull timeContract work
- ...The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation...SuggestedPermanent employmentFull timeContract workInterim roleWork from homeFlexible hoursAfternoon shift
- Sr Statistical Programmer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer... ...provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the...SuggestedFull timeContract work
