Related skills
project management vendor management clinical trials data reporting ctmsπ Description
- Lead cross-functional teams and vendors to ensure study delivery from start-up to close-out.
- Act as client liaison; manage contractual, organizational, and relationship needs.
- Prepare and deliver study updates, dashboards, and reports to teams, management, sponsors.
- Update project management systems weekly; serve as escalation point for team.
- Forecast resources/hours, review hours, and manage scope changes with client and PM Director.
- Organize operational plans, oversee study operations per regulations and SOPs.
π― Requirements
- Strong written and verbal communication; excellent presentation skills.
- Knowledge of clinical trial regulations; virtual/DCT experience preferred.
- Experience with a CTMS platform or equivalent.
- Interpersonal, collaboration, and time-management strengths.
- Undergraduate health degree + 5+ years clinical research experience; CRO/SMO/Sponsor preferred.
- Willingness to travel ~30% and work across time zones.
π Benefits
- Top notch healthcare (medical, dental, vision) for you and family.
- 100% 401(k) company match up to 4% with immediate vesting.
- Company provided laptop, your choice of PC or Mac.
- Monthly stipend for internet and phone expenses.
- Short & long-term disability and life insurance.
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