Offer summary
Qualifications:
Bachelor’s degree in health or life science related field, 1.5 to 5 years experience in clinical monitoring, Willingness to travel nationally, Familiarity with Microsoft® Office, Strong communication and presentation skills.
Key responsabilities:
- Conduct visits for research sites in compliance with approved protocol
- Communicate with medical site staff and ensure good documentation practices
- Verify investigator qualifications and enrollment of eligible subjects
- Review regulatory documents, adverse events and data reporting
- Assess patient recruitment success and offer suggestions for improvement