Clinical Development Scientist, Senior Manager

Demonstrated experience in clinical development within the pharmaceutical/biotechnology industry is required.

Strong understanding of the drug development process, clinical trial design, and execution.

Excellent knowledge of clinical procedures, ICH guidelines, and Good Clinical Practice (GCP).

Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

Learn more at Pfizer Candidate Site – U.S.

Pfizer compensation structures and benefit packages are aligned based on the location of hire.

Maintains current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.

Authors and reviews key clinical and regulatory documents including, but not limited to, protocols, study-level informed consent forms (ICFs), Investigator's Brochures (IBs), clinical study reports (CSRs), and regulatory submission components.

Leads the clinical data review strategy, including the ongoing review of emerging clinical data for safety and efficacy trends.

Presents relevant data to internal teams, governance bodies, and other stakeholders.

Collaborates with cross-functional team members (e.g., Clinical Operations, Biostatistics, Regulatory Affairs, Clinical Pharmacology) to ensure trial objectives are met and activities are executed seamlessly.

Provides scientific and clinical input for site training materials and supports responses to questions from investigators and site personnel regarding the protocol and study conduct.