Job Summary
The Senior Clinical Research Associate is accountable for conducting both on-site and remote monitoring visits to verify the suitability and regulatory compliance of investigational sites. This role also involves providing training to site personnel and offering guidance to junior colleagues during co-monitoring activities.
Responsibilities
- Conduct on-site and remote monitoring to assess compliance and site readiness.
- Train site staff to ensure proper understanding of protocols and procedures.
- Mentor junior team members through co-monitoring experiences.
Qualifications
- A degree in Life Sciences or an equivalent level of experience is required.
- Significant on-site monitoring experience in phase 2/3 clinical trials is essential.
- Experience in oncology or rare disease studies is highly preferred.
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.
