Job Description:
EPM Scientific is representing a global, science-driven oncology company dedicated to discovering and developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With one of the largest oncology/hematology research teams in the world, they are committed to addressing a broad range of cancers through our extensive pipeline of cutting-edge therapies.
The successful candidate will play a pivotal role in providing statistical leadership and support for clinical development programs. This position requires a deep understanding of biostatistics, strong analytical skills, and the ability to work collaboratively with cross-functional teams.
Key Responsibilities:
- Provide statistical leadership and guidance for clinical development programs.
- Develop and implement statistical analysis plans for clinical trials.
- Collaborate with clinical, regulatory, and data management teams to ensure the integrity and accuracy of clinical data.
- Perform statistical analyses and interpret results to support clinical trial reports and regulatory submissions.
- Ensure compliance with regulatory requirements and industry standards.
- Mentor and provide guidance to junior biostatisticians.
- Stay current with advancements in biostatistics and clinical trial methodologies.
Qualifications:
- Ph.D. or Master's degree in Biostatistics, Statistics, or a related field.
- Minimum of 8 years of experience in biostatistics within the pharmaceutical or biotechnology industry.
- Proven track record of successful regulatory submissions.
- Strong knowledge of statistical software (e.g., SAS, R).
- Excellent communication and interpersonal skills.
- Ability to work effectively in a team-oriented environment.
- Strong problem-solving and analytical skills.
