Related skills
documentation data management gcp project management clinical trials📋 Description
- Lead trial delivery across full lifecycle (feasibility to close-out)
- Draft documents, prepare submissions, TMF setup/maintenance
- Coordinate data management activities and site setup
- Manage sites from feasibility to close-out with documentation
- Maintain regulatory files (eTMF) and audit-ready docs
- Communicate with sponsors, sites, and vendors; keep stakeholders updated
🎯 Requirements
- 2-3+ years in clinical research ops or related roles
- Background in a research or healthcare environment
- Strong project management with detail-oriented docs
- Excellent communicator; build relationships with stakeholders
- Solutions-focused, proactive; escalate issues when needed
- Work independently; manage multiple priorities remotely
🎁 Benefits
- Competitive salary plus meaningful equity
- $2,000 annual Learning & Development budget
- 39 days annual leave (PTO + holidays + James Lind Day)
- $800 monthly employer insurance contribution
- $40 monthly wellness allowance and Happl membership
- Monthly lunch vouchers for remote team members
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