Related skills
gcp edc pharmacovigilance ip tmf📋 Description
- Independently oversee site management and patient safety.
- On-site monitoring and routine/close-out visits per protocol.
- Manage site startup, EC/IRB submissions, and regulatory docs.
- Support trial budgets, investigator contracts, and IP coordination.
- Data review, SAE processing, and pharmacovigilance activities.
🎯 Requirements
- Bachelor’s degree or international equivalent in science/healthcare.
- 3.5+ years on-site monitoring; Oncology and global trial experience.
- Proficient in Microsoft Office (Outlook, Word, Excel, PowerPoint).
- Fluent English; strong attention to detail; customer service demeanor.
- Knowledge of drug development process; willingness to travel 60-70%.
- Preferred: solid clinical research experience; strong organizational skills; remote work ability.
🎁 Benefits
- Mentoring and development opportunities for junior staff.
- Remote-friendly work environment.
- Collaborative, global project teams and cross-functional work.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Healthcare Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!