responsible for :
- Supporting study operational activities under the direction of the clinical study lead
- Assisting with trial related tasks including oversight and management of CROs and other study vendors
- Providing support to ensure that studies are completed on time, within budget, and in compliance with SOPs and applicable regulatory requirements
- Maintaining study registries and dashboards
- Approx. 20% travel depending on study / project needs
An ideal candidate for this role MUST have
- 4 years of industry experience REQUIRED
- 2 years oncology experience
- Global trial experience preferred
- A Bachelor's degree in Biological Sciences, Nursing, Pharmacy or a related discipline
- A working knowledge of ICH GCP guidelines
Benefits :
- Pre-IPO biotech company
- Competitive salary with comprehensive benefits (90% medical coverage)
- Flexible PTO and WFH arrangements
- 401K contribution
- Cell phone reimbursement, life insurance, and additional perks
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