Site Budget and Contract Specialist - FSP Model
Fortrea
DenmarkPosted 17 days agoDiscoveredMatch locked
RemoteFull Time
Join Our Team and Shape the Future of Clinical Research!
At
Fortrea
, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a
Site Budget & Contract Specialist
, you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.
In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.
Preferred Candidate Profile
Able to support contract and budget activities across
Finland, Sweden and Norway
.
In this role, you will
- Prepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials.
- Ensure compliance with SOPs, regulatory guidelines, and contractual obligations.
- Track, update, and maintain contract status in relevant systems, ensuring transparency and timely execution.
- Identify and escalate contractual issues to management as needed.
- Support the internal review, revision, and approval process of contracts before forwarding them to external parties.
- Collaborate with clinical study teams, legal, and project management to ensure seamless contract execution.
- Maintain electronic and paper contract files, ensuring accuracy and accessibility.
- Assist in the continuous improvement of departmental processes and procedures.
- Provide regular status updates to management and study teams.
Required Qualifications
To succeed in this role, you should have:
•
Bachelor’s degree (LLB, JD, BA, or BS) preferred
; a university-level law degree is highly desirable.
- Fortrea may consider
equivalent relevant experience
in lieu of educational requirements.
•
2–4 years of experience
in contract negotiation, clinical research, or a related field.
- Strong understanding of
ICH GCP guidelines
and clinical research processes.
- Excellent
negotiation, communication, and organizational skills
.
- Ability to work
independently and manage multiple priorities
in a fast-paced environment.
- Proficiency in Microsoft Office and contract tracking systems.
•
What We Offer
- Competitive salary and performance-based incentives.
- Flexible work arrangements (remote/hybrid options).
- Professional growth opportunities in a collaborative and innovative environment.
- The opportunity to work on cutting-edge clinical research projects.
Ready to Make an Impact?
Take the next step in your career and join us in driving innovation in clinical research.
Apply today!
Applications are reviewed on a rolling basis—don’t miss this opportunity!
Learn more about our EEO & Accommodations request here.
Originally posted on Himalayas
Not included in the source posting: what you'll do.
Skills
gcp
Who can apply
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