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Medical Monitor – Study Physician – Medical Director
ParexelStudy Physician at Parexel responsible for medical oversight and expertise in clinical trials. Ensuring high quality trial protocols and contributing to risk management in a clinical development setting.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial management, including protocol development, risk management, and medical oversight. Possesses strong knowledge of ICH-GCP regulations and experience in clinical development within the pharmaceutical industry.
Highest-signal resume keywords
Physician (MD)Clinical Development ExperienceMedical Monitoring ExperienceUnderstanding of ICH-GCPExperience in Pharma Industry or CRO
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial Protocol DevelopmentRisk ManagementMedical Data ReviewClinical Quality MonitoringData Visualization Systems
Tools & Technologies
IT Systems
Industry Keywords
PulmonologyImmunologyInternal MedicineInfectious DiseasesFamily MedicinePediatricsRheumatologyEmergency MedicinePharmacovigilanceClinical Trials
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial
- Provide medical expertise and medical oversight from the Trial Design Outline to the Clinical Trial Report
- Ensure timely preparation of high medical quality clinical trial protocols
- Contribute to trial risk-based quality management by defining medically relevant data and related risks integrated into the quality and risk management plan
- Co-author Clinical Quality Monitoring plans
- Perform ongoing reviews of medical data
Requirements
What you’ll need- Physician (MD) ideally with medical thesis
- Minimum of 4 years of active clinical practice experience
- Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology or Emergency Medicine
- Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions ideally in Clinical Development
- Understanding of relevant regulations and guidance including ICH-GCP
- Ideally previous experience as a medical monitor
- Experience with data visualization systems and IT systems
- Clinical development/trials experience
Benefits
Comp & perks- Health insurance
- Competitive salary
- Flexible working hours
- Professional development opportunities