Soc/Clin Research Specialist
About The Position
This position will entail direction of numerous industry sponsored clinical trials and other research projects at the Thurston Arthritis Research Center. Key aspects of the position will include communication and coordination with industry sponsors, research organizations and other sites as necessary. The position will be responsible for IRB submissions, contract negotiations, and all regulatory documentation as well as patient recruitment, patient evaluations, collection and management of all study data. The coordinator will coordinate and perform study specific regulatory processes across multiple studies of different therapeutic areas and phases, in accordance with appropriate regulations, Standard Operating Procedures, and study specific protocols. The Clinical Trials Study Coordinator will also participate in other clinical research activities as necessary at the Thurston Arthritis Research Center.
Responsibilities
- Direction of numerous industry sponsored clinical trials and other research projects
- Communication and coordination with industry sponsors, research organizations and other sites
- IRB submissions
- Contract negotiations
- All regulatory documentation
- Patient recruitment
- Patient evaluations
- Collection and management of all study data
- Coordinate and perform study specific regulatory processes across multiple studies of different therapeutic areas and phases
- Participate in other clinical research activities as necessary
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
