Clinical Trial Specialist
2 weeks ago
About the Role:
We are seeking a highly skilled and experienced Clinical Trial Specialist to join our team. In this role, you will be responsible for providing administrative support to the clinical study team, ensuring that clinical trials are run according to protocol, and managing documentations.
The ideal candidate will have a strong educational background in life sciences or as a licensed healthcare professional, excellent interpersonal skills, proficiency in MS Office, and the ability to manage multiple priorities simultaneously.
Key Responsibilities:
- Providing ongoing administrative support to the clinical study team
- Collaborating with site staff to ensure clinical trials are being run according to the protocol
- Document management, tracking, electronic filing and review
- Responsible for IRB/EC submission, from initial submission to amendment
You Will Enjoy This Role If:
- You are detail-orientated, passionate, and reliable
- You have experience working on oncology trials
- You are able to manage multiple priorities simultaneously
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