Sr Site Contract Specialist

ThermoFisher Scientific; Colombia; Remote; COP 60,000,000 - 120,000,000; Full time

Job summary

Thermo Fisher Scientific's Clinical Research team seeks a Senior Site Contract Specialist to drive site contracts and budgets for clinical trials, partnering with investigators, sponsors, and legal teams.

You will ensure timely contract execution, assess risks, and maintain documentation to support study start-up milestones in a global, fast-paced environment.

Qualifications

• Bachelor’s degree or equivalent combination of education, training, and relevant experience.
• Understanding of clinical research, site activation processes, and contract management principles.
• Experience in contract negotiation and site contracting within pharma/biotech environments.
• Excellent English communication and strong interpersonal skills.

Responsibilities

• Draft, review, negotiate, and finalize site agreements per local regulations and client requirements.
• Lead investigators grant and budget negotiations within approved parameters.
• Ensure compliance with contractual processes and approval requirements.
• Assess and escalate legal, financial, and operational risks as appropriate.
• Collaborate with internal stakeholders to align activities with site activation timelines.
• Maintain accurate documentation and tracking of contractual activities in company systems.

Skills

Negotiation

Contract management

Risk assessment

English communication

Time management

Cross-functional collaboration

MS Office

Education

Bachelor’s degree

Tools

Contract management systems

Microsoft Office

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Sr Site Contract Specialist

Make an Impact at the Forefront of Innovation

At Thermo Fisher Scientific, our Clinical Research team supports leading pharmaceutical, biotechnology, and emerging biopharma companies in advancing innovative therapies worldwide. Having contributed to thousands of clinical trials across more than 100 countries, we are committed to accelerating research that improves patient lives.

As a Senior Site Contract Specialist, you will play a critical role in the successful start-up and execution of clinical trials by leading site contract and budget negotiations. Working closely with investigative sites, sponsors, legal teams, and internal stakeholders, you will help ensure efficient contract execution while balancing compliance, risk management, and study timelines.

Position Summary

The Senior Site Contract Specialist is responsible for drafting, reviewing, negotiating, and finalizing clinical trial agreements and investigator budgets in accordance with company, client, and local requirements. This role serves as a key partner in the site activation process, ensuring contractual activities are completed efficiently while identifying and mitigating legal, financial, and operational risks. The position requires strong negotiation skills, attention to detail, and the ability to collaborate across multiple functions to support study start-up objectives.

Key Responsibilities

• Draft, review, negotiate, and finalize agreements with investigative sites in accordance with local regulations, company policies, and client requirements.
• Lead investigators grant and budget negotiations within approved parameters and escalation pathways.
• Ensure compliance with contractual processes, negotiation guidelines, approval requirements, and client expectations.
• Assess and Escalate legal, financial, and operational risks as appropriate.
• Provide recommendations and alternative solutions to facilitate contract negotiations and issue resolution.
• Collaborate with internal stakeholders to align contractual activities with site activation timelines and study objectives.
• Support achievement of study start-up and site activation milestones through efficient contract execution.
• Ensure adherence to budgetary guidance, templates, and contractual standards.
• Maintain accurate documentation and tracking of contractual activities within company systems.
• Facilitate effective communication among study sites, sponsors, legal teams, and operational stakeholders.
• Support continuous process improvement initiatives and promote best practices in contract management.
• Ensure contractual risks and outstanding issues are proactively identified, reviewed, and managed.

Minimum Qualifications

• Bachelor’s degree or equivalent combination of education, training, and relevant experience.
• Understanding of clinical research, site activation processes, and contract management principles.

Experience

Relevant experience in contract negotiation, site contracting, clinical operations, legal support, or related functions within a pharmaceutical, biotechnology, CRO, or healthcare environment.

Candidates will be considered based on their experience, qualifications, and demonstrated expertise in clinical trial agreements, budget negotiations, and risk assessment.

Preferred Skills & Competencies

• Understanding of contract law principles and regulations impacting clinical trial agreements.
• Knowledge of investigator grant and budget negotiation processes.
• Understanding of business, financial, and operational considerations related to clinical research contracts.
• Strong negotiation, analytical, and problem-solving skills.
• Excellent attention to detail and risk assessment capabilities.
• Effective written and verbal communication skills in English.
• Strong organizational and time management skills.
• Ability to manage multiple priorities and deadlines in a dynamic environment.
• Ability to work independently and collaboratively across cross-functional teams.
• Customer-focused approach to communication, issue resolution, and stakeholder management.
• Proficiency with Microsoft Office and contract management systems.

Working Conditions & Environment

• Work is performed in an office and/or home-based environment with exposure to standard office equipment and technology.
• May collaborate with global teams across multiple time zones.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.