Job Summary
The position involves conducting both on-site and remote monitoring tasks across all phases of clinical trials, ensuring adherence to regulatory standards. The candidate will assist in regulatory submissions while also providing guidance and training to junior team members.
Responsibilities
- Conduct on-site and remote monitoring activities throughout various stages such as pre-study, initiation, interim, and close-out visits.
- Ensure compliance with regulatory requirements at study sites.
- Support the preparation and submission of regulatory documents.
- Mentor and train junior staff members in monitoring processes and procedures.
Qualifications
- A college or university degree in Life Sciences is required.
- Extensive on-site monitoring experience in phase 2/3 clinical trials is essential.
- Prior involvement with complex clinical trials, particularly in oncology or rare diseases, is preferred.
- Strong communication skills are necessary for effective collaboration and mentorship.
Ergomed provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
