Bristol Myers Squibb Company

Senior Clinical Scientist, Early Development

Location
Princeton, NJ, United States
Posted
Aug 20, 2020
Ref
R1522291
Required Education
Bachelors Degree
Position Type
Full time
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

The Clinical Research Scientist (CRS) leads the clinical science aspects of early development clinical trials in hematology, oncology and/or cellular therapy. The CRS will provide the scientific expertise and in partnership with the medical lead and cross functional team develop and execute early development clinical studies. Key responsibilities include: authoring of study protocol/amendments and other clinical trial documentation (e.g. IND/CTA, informed consent forms, study reports), clinical data review, presentation/publication of results and clinical trial site interactions.

Position Responsibilities:
  • Provide the scientific expertise necessary to develop and execute early development clinical studies in hematology and oncology indications
  • Represent Early Clinical Development in cross-functional teams/meetings both internally and externally
  • Contribute to the authorship/review and amendment of clinical study protocols, consent forms, case report forms, publications and other clinical study documents (IND/CTA) in collaboration with the medical lead and cross-functional study teams
  • Collaborate with cross-functional study team including clinical operations, data management and the medical lead in the review, querying and reconciliation of clinical data. Prepare data summaries and presentations as needed.
  • Primary clinical expert for clinical trial sites and study teams for assigned studies
  • Intermittent travel to clinical sites and professional meetings and congresses required


Desired Experience:
  • Bachelor's degree required; Master's degree, PhD or PharmD preferred
  • Minimum 4 years prior experience in related biomedical research in industry or academia
  • Ability to plan, develop, and execute early clinical development oncology, cell therapy and/or hematology studies including analysis, interpreting, and reporting results
  • Applicants should have strong leadership skills, yet be able to work effectively in a team environment
  • Excellent communication and presentation skills are essential


Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.