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About the role
Key responsibilities & impact- Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards
- Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures
- Build and manage strong relationships with trial investigators and stakeholders
- Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management
Requirements
What you’ll need- University degree in medicine, science, or equivalent combination of education & experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- Willingness to travel as required (approximately 25%)
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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 trial managementprotocol developmentrisk managementvendor selectionmonitoring experiencetherapeutic area expertise
Soft Skills
problem-solvingdecision-makingcollaborationrelationship management
Certifications
university degree in medicineuniversity degree in science