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Key responsibilities include serving as the responsible biostatistician on clinical trials, contributing to clinical study protocols, and reviewing and interpreting results from simple to complex clinical studies.
Job Requirements:
- Must have PhD in statistics or biostatistics or related subjects and 5+ years of experience as a biostatistician in CRO or Pharmaceutical companies OR Masters degree in statistics or biostatistics or related subjects and 10+ years of experience as a biostatistician in CRO or Pharmaceutical companies.
- Thorough knowledge of and experience with CDISC standards and regulatory requirements.
- Experience in working on Phase 2 and 3 studies, R programming, ESTIMANDS, and adaptive designs.
- Strong leadership and communication skills, including the ability to write SAP and create analysis for publications.
- Knowledge of ADAM and TFL programming.
We Are Looking For:
- Candidates with strong analytical and problem-solving skills, who can work effectively in a team environment.
- Individuals who are passionate about delivering high-quality results and making a meaningful contribution to the organization.
About Our Organization:
- We are a leading provider of contract research services, dedicated to helping pharmaceutical and biotechnology companies bring innovative treatments to market.
- We are committed to fostering a diverse and inclusive workplace culture, where employees feel valued and supported.