Staff Research Associate III
About The Position
This position will serve as a senior clinical research coordinator for a diverse portfolio of research activities for multiple studies. The portfolio may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, large research grant awards, laboratory-based research, and/or programmatic clinical research activities, such as a clinical database and biorepository. Incumbent will oversee timelines and milestones to ensure that targeted deadlines are met facilitating the development and deployment of educational and training materials for all team members, keeping regulatory and budgetary documents compliant, assisting with the preparation of progress reports, implementing quality assurance standards and liaising with other core/components of studies. The individual should be knowledgeable of the principles of scientific investigation and clinical trials, and capable of in-depth understanding of study protocols.
Requirements
- Master’s degree or Bachelor’s degree with research experience required
- At least 3 years of clinical trials experience
- At least 2 years of regulatory work experience in clinical trials
- Excellent organizational and communication skills (both written and verbal)
- Strong attention to detail
- Flexibility to work both independently and collaboratively
- Understand critical aspects of clinical trials including tracking, enrollment, retention, regulatory compliance and data management
Nice To Haves
- 1 year of industry trial experience preferred
- Prior experience being part of an academic clinical research group preferred
Responsibilities
- Performs clinical trial project coordination at the SFVA Hematology/Oncology Research Program
- Contributes to the development of protocols, related documents, manuscripts, and Case Report Forms
- Assist in preparation of new IRB applications and shepherd through to completion; arrange paperwork for renewal of existing protocols; respond to IRB requests for revisions; and coordinate protocol changes with study sponsors.
- Aids with managing Principal Investigator lab and biospecimen studies and coordinating crosscutting efforts of bench science with clinical trials.
- Assist with preparation of grant applications, including revisions and progress reports, manuscript and scientific abstract preparation; additional administrative
Benefits
- bonuses
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What This Job Offers
Job Type
Full-time
Career Level
Senior
