Start-Up Associate Contractor (Spain)
Allucent
Clinical OperationsCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Allucent seeks a Start-Up Associate Contractor to coordinate clinical trial site initiation activities across regulatory, ethical, and contractual domains. The role involves managing documentation, communicating with regulatory authorities and ethics committees, and supporting pre-study activities for biopharmaceutical trials in Spain on a 0.5 FTE hybrid/remote basis.
What they're looking for
- Life science degree or equivalent qualification in related allied health profession
- Experience with clinical trial management systems and electronic trial master files
- Knowledge of regulatory submissions and ethics committee processes
- Proficiency in contract negotiation and clinical trial agreement management
- Strong organizational and tracking skills with attention to documentation detail
What you'll be doing
- Track start-up milestones and document progress in CTMS and related tracking systems
- Prepare, compile, and submit regulatory documentation to authorities and ethics committees
- Prepare answers to regulatory and ethics committee inquiries and coordinate submissions
- Negotiate and finalize clinical trial agreements, budgets, and site contracts within approved parameters
- Collect and review essential documents from sites with follow-up on discrepancies
Privacy & handoff
This role links to Allucent's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.