Clinical Research Associate
hace 1 mes
About this role:
The In-House Clinical Research Associate supports the Global Clinical Operations (GCO) Center of Excellence, conducting activities consistent with GCO's mission of building a world-class shared clinical technology, process innovation, and clinical operations team, in partnership with the company's divisions, through technology enablement, high-touch customer service, study acceleration, and high-quality data collection.
Key Responsibilities:
- Work independently and proactively to coordinate all necessary activities for site regulatory submissions and essential document collection for allocated clinical research sites.
- Manage multiple sets of essential regulatory documents across several studies and division portfolios.
- Partner with clinical sites to support the negotiation and customization of Informed Consent Form (ICF).
- Develop and foster clinical research site relationships to become a subject matter expert in the site start-up regulatory process across multiple studies.
- Manage to achieve target IRB / EC timelines by assisting clinical research sites with the application submission process and approval tracking.
- Manage and problem-solve site start-up challenges that arise to mitigate impact to service level agreements and study goals.
What Boston Scientific Offers:
- Access to the latest tools, information, and training to advance your skills and career.
- A supportive environment to progress your ambitions.
- The opportunity to work in teams of diverse and high-performing employees.
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