Salary: $95 - $115K
Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Associate to facilitate their in house studies.
The CRA will be responsible for:
- Managing study sites and investigating clinical trials and/or post-authorization safety studies
- Performing and coordinating different aspects of clinical monitoring and site management
- Site setup, initiation, close-out and management (including monitoring) of sites participating in clinical and
post-authorisation studies on an as needs basis - 50% travel
An ideal candidate for this role MUST have…
- 2+ years of ONSITE monitoring experience at a sponsor or CRO
- A Bachelor's degree in Biological Sciences, Nursing, Pharmacy or a related discipline
- A working knowledge of ICH GCP guidelines
Benefits:
- Competitive salary with benefits
- High degree of commercial exposure early in your career
- Being a part of team whose work directly aims to improve the quality of people's lives
- Great work-life balance
If you are interested in this Clinical Research Associate role, don't hesitate to reach out!