What are the responsibilities and job description for the Clinical Research Coordinator position at Actalent?
Work on Oncology-based studies!
Long-Term Opportunity
Competitive Pay
40 Hours, No Weekends!
Qualifications:
- 1-3 years of Clinical Research Coordinator experience
Responsibilities:
- Coordinates, implements, and evaluates clinical research trials, studies, and projects.
- Recruits and screens potential study participants and develops/conducts patient and family education accordingly.
- Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures.
- Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.
- Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations provides leadership in identifying and implementing corrective actions/processes.
- Monitors IRB submissions and responds to requests and questions.
- Interfaces with study sponsors, monitors and reports SAEs resolves study queries.
- Assists in developing grant proposals and protocols.
**For a quicker response, please send most updated resumes to mknowlton@actalentservices.com**
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.
