Role OverviewAs a Clinical Research Associate, you will serve as the primary point of contact between investigation sites and the sponsor for early development multi-therapeutic clinical trials. You will conduct site visits, ensure site compliance, and maintain documentation in CTMS and eTMF systems.
What You Will Do
Your main responsibilities will include conducting site visits, ensuring site compliance with ICH-GCP, SOPs, and regulations, maintaining up-to-date documentation, and supporting subject recruitment and retention efforts.
Why It Might Be a Fit
To be successful in this role, you will need to be a clear communicator, problem-solver, and collaborative team player. You will also need to be proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF.
Requirements
- Bachelor's degree in Life Sciences or equivalent
- Eligible to work in the United States without visa sponsorship
- 0 to 6-month provider-specific academy or <2 years of clinical trial monitoring experience or equivalent industry experience
- Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
Benefits
- Competitive base salary
- Performance-related incentives
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities
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