What are the responsibilities and job description for the Regulatory Specialist position at Actalent?
This opportunity is with a top Academic Research Institute looking to add a Regulatory Coordinator to their Cancer Center research team!
Description:
Process all initial regulatory documents for submission to the Pharmaceutical Sponsors and Institutional Review Board (IRB)
Prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees
Prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations (CROs), the NCI and the FDA.
Additional Skills and Qualifications:
- Bachelors Degree required
- Minimum of 3 years of clinical research experience needed
- Drug Trial experience – oncology preferred
- Hands on experience working with IRB regulatory submissions
- Critical thinker, progressive, and takes initiative
Experience Level:
Intermediate Level
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.
Salary : $20 - $31