The Site Budget & Contracts Specialist is responsible for drafting negotiating and managing site agreements and related clinical trial contracts for Sponsor-led studies. The role ensures timely execution of agreements compliance with SOPs and ICH-GCP principles and close collaboration with crossfunctional clinical study teams.
Key Responsibilities
- Draft review negotiate and process site agreements templates and related clinical trial contracts in accordance with Fortrea policies and Sponsor requirements.
- Manage the full contract lifecycle including tracking approvals execution filing and status updates using SAMS or equivalent systems.
- Independently manage assigned studies while ensuring strict adherence to SOPs quality standards and regulatory requirements.
- Identify contractual risks or operational delays early and escalate issues proactively to ensure timely resolution.
- Coordinate with clinical study teams project management business development and budget teams to align contract timelines and expectations.
- Provide regular and accurate contract status updates to management and internal stakeholders.
- Contribute to departmental objectives process improvements and support junior colleagues as required.
Experience & Qualifications
- 3 - 5 years experience in clinical contracts site agreements or contract administration within a CRO or pharmaceutical environment.
- Demonstrated experience in contract drafting negotiation and lifecycle management.
- Solid knowledge of ICH-GCP SOP-driven environments and clinical trial regulations.
- Bachelors degree preferred (Law Business or Life Sciences); law degree (EU) is an advantage.
- Strong organizational skills with the ability to manage multiple studies simultaneously.
This is an excellent opportunity to contribute to global clinical studies while further developing your clinical contracts expertise within a dynamic CRO environment.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
The Site Budget & Contracts Specialist is responsible for drafting negotiating and managing site agreements and related clinical trial contracts for Sponsor-led studies. The role ensures timely execution of agreements compliance with SOPs and ICH-GCP principles and close collaboration with crossfunc...
The Site Budget & Contracts Specialist is responsible for drafting negotiating and managing site agreements and related clinical trial contracts for Sponsor-led studies. The role ensures timely execution of agreements compliance with SOPs and ICH-GCP principles and close collaboration with crossfunctional clinical study teams.
Key Responsibilities
- Draft review negotiate and process site agreements templates and related clinical trial contracts in accordance with Fortrea policies and Sponsor requirements.
- Manage the full contract lifecycle including tracking approvals execution filing and status updates using SAMS or equivalent systems.
- Independently manage assigned studies while ensuring strict adherence to SOPs quality standards and regulatory requirements.
- Identify contractual risks or operational delays early and escalate issues proactively to ensure timely resolution.
- Coordinate with clinical study teams project management business development and budget teams to align contract timelines and expectations.
- Provide regular and accurate contract status updates to management and internal stakeholders.
- Contribute to departmental objectives process improvements and support junior colleagues as required.
Experience & Qualifications
- 3 - 5 years experience in clinical contracts site agreements or contract administration within a CRO or pharmaceutical environment.
- Demonstrated experience in contract drafting negotiation and lifecycle management.
- Solid knowledge of ICH-GCP SOP-driven environments and clinical trial regulations.
- Bachelors degree preferred (Law Business or Life Sciences); law degree (EU) is an advantage.
- Strong organizational skills with the ability to manage multiple studies simultaneously.
This is an excellent opportunity to contribute to global clinical studies while further developing your clinical contracts expertise within a dynamic CRO environment.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
View more
View less