Clinical Study Trial Operations Specialist
2 tygodni temu
At Fortrea, we are searching for a highly motivated Clinical Study Trial Operations Specialist to join our team. As a Clinical Study Trial Operations Specialist, you will play a vital role in preparing and negotiating site agreements, confidentiality agreements, letters of indemnification, and other contracts for sponsors who contract Fortrea to perform this service.
Responsibilities:
* Responsible for adherence to standard operating procedures (SOPs).
* Perform daily tracking, negotiation, and approval of Site Agreements and Site Agreement templates for clinical study teams.
* Timely update the departmental Site Agreement.
* Perform contract administration functions including assisting with obtaining approvals on authorization forms as required.
* Maintain a contract tracking system to report contract status updates and signing status.
* Provide notice of all executed contracts to the appropriate team members along with contract values.
* Scan and file executed contracts in the shared electronic storage area in a timely manner for access by other staff members.
* Draft, negotiate, review, and process contracts in a commercially reasonable manner that protects Fortrea's fundamental interests and in accordance with departmental practices and policies.
* Negotiate contractual terms with other contracting parties in a professional manner.
Qualifications:
* Bachelor's degree preferred.
* Minimum 0-2+ years of experience, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
About Fortrea:
Fortrea is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
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