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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Provides medical monitoring on one or more clinical trials
- Provides timely, study-related medical information and guidance
- Contributes to medical assessments of Quality Events
- Conducts and documents periodic safety data review and ongoing clinical/medical data review
- Reviews Required Safety Text for the Informed Consent Document
- Provides clinical support for one or more studies
- May provide input to the protocol design document
- Supports the study team in internal protocol review governance submissions and interactions
- May develop Study Informed Consent Documents
- Provides clinical input to the development of the Statistical Analysis Plan
- Ensures all clinical queries are appropriately addressed in support of database lock
- Tracks and reconciles Serious Adverse Events
- Contributes to site selection criteria
- May serve as a clinical point of contact with investigators and study team for questions relating to clinical aspects of the protocol
Requirements
What you’ll need- Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university
- Licensed by a licensing body/health authority to prescribe medicines independent of supervision for at least 2 years post their intern/house officer/foundation period
- Cardiometabolic disease experience, e.g., obesity, diabetes, endocrinology
- Maintained registration/Medical License to practice and always in good standing with their Medical Licensing Authority
- Clinical research experience in the biopharmaceutical industry in study design, start-up, conduct, and close-out, including regulatory submissions and inspections
- Scientific productivity via publications, posters, abstracts and/or presentations
- Knowledge of clinical development, global and regional regulation, and ICH/GCP
- Clinical and administrative capabilities; effective verbal and written communication skills
- Track record of achievement in pharmaceutical development
Benefits
Comp & perks- 401(k) plan with Pfizer Matching Contributions
- Pfizer Retirement Savings Contribution
- Paid vacation
- Holiday and personal days
- Paid caregiver/parental and medical leave
- Health benefits including medical, prescription drug, dental and vision coverage
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical monitoringmedical assessmentssafety data reviewclinical data reviewprotocol designStatistical Analysis Plandatabase lockSerious Adverse Events trackingsite selection criteriaclinical research
Soft Skills
effective communicationclinical supportteam collaborationproblem-solvinginterpersonal skillsorganizational skillsleadershipattention to detailcritical thinkingadaptability
Certifications
MDDOMBBSMBChBMedical License
