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About the role
Key responsibilities & impact- Leading global, cross-functional observational study teams
- Owning delivery of contracted scope, timelines, and quality
- Developing study documentation, including project management plans
- Monitoring study progress and financial performance
Requirements
What you’ll need- Bachelor's degree in life sciences or related field
- Minimum 4-6 years of experience in project management and/or clinical operations within pharma, CRO, or RWE environment
- Demonstrated experience leading observational or real-world evidence studies
- Strong understanding of RWE study designs and clinical research conduct
- Experience with primary and secondary data study designs
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development opportunities
- Bonuses
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
project managementclinical operationsobservational studiesreal-world evidence studiesdata study designs
Soft Skills
leadershipcommunicationorganizational skills
Certifications
Bachelor's degree in life sciences