Accountable for the scientific integrity of the study and the well-being of the patients enrolled in one or more clinical trials
Applies technical and clinical skills to ensure the design of efficient and high-quality clinical trials
Responsible for effective execution of studies and works in close partnership with other clinical and medical colleagues, clinical operations, and other functional lines
Accountable for timely delivery of a quality protocol, clinical execution of clinical trials, and supports appropriate interpretation and communication of clinical trial data
Maintains compliance with internal and external standards and proactively mitigates risk
Primary contact with external investigators & internal study team for clinical aspects of the protocol
Provides clinical input to support development of protocol design document (PDD)

Requirements

BA/BS or equivalent qualification with 6+ years of experience in biopharmaceutical industry in clinical research and development
MBA or MS equivalent with 5+ years of experience
Advanced Degree with 1+ years of experience
Demonstrated clinical, administrative, and project management capabilities
Excellent verbal and written communication skills in English
Clinical research experience in phase 3/pivotal space highly preferred
Cardiometabolic disease experience highly preferred (ie; cardiology, obesity, endocrinology, nephrology etc)
Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management

Benefits

Comprehensive and generous benefits
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Medical, prescription drug, dental and vision coverage

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical researchprotocol designproject managementadverse event managementclinical trial executionclinical trial data interpretationbiopharmaceutical developmentregulatory complianceICHGCP

Soft Skills

communication skillscollaborationproblem-solvingrisk mitigationadministrative skillsleadershiporganizational skillsattention to detailinterpersonal skillstime management