Clinical Research Coordinator - Knoxville, TN
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Job Description:
Looking to hire an individual with clinical research experience to act as a consultant CRC to support am ongoing clinical trial. The main job duties for this position will be regulatory filing, creating source documents, data entry (EDC), along with patient recruitment and other research administrative duties.
*This role requires research experience*
Duties and Responsibilities
- Data Entry/Management
- Collection of study data and entering data into EDC (as well as keep EDC up to date)
- Creating source documents
- Chart review/phone screening
- Study administration
- Any study efforts deemed necessary by site
Requirements:
- Clinical Research Experience
- Highly independent
- Willing to obtain Good Clinical Practices (GCP) certified
*This position is not remote*
Recruiter: Shelby Ciardelli (763) 923-2058 [email protected]
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.