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Contract Coordinator

ThermoFisher Scientific

Wilmington, NCContractSeen 2w ago

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At a glance

Compensation
No compensation found
Location
Wilmington, NC
Schedule
Contract
Work Authorization
Not specified

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Job overview

Thermo Fisher Scientific seeks a Contract Coordinator to manage clinical trial agreements, facilitate documentation, and support international clinical trials. The role involves building relationships with research sites, ensuring compliance with SOPs and regulatory requirements, and contributing to the advancement of global healthcare initiatives.

Skills & qualifications

RequiredNice to have

Skills

English Language ProficiencyMicrosoft OfficeWordExcelClinical Trial Agreement ProcessesBudget Preparation and NegotiationOrganizational SkillsAttention to DetailIndependent WorkTeam CollaborationSOPs and Regulatory KnowledgeDocument Management SystemsElectronic Signature PlatformsCustomer Service OrientationInterpersonal SkillsAccurate Records Maintenance

Qualifications

1 Year Relevant ExperienceLegal Background

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join our Global Site Contracts Team at Thermo Fisher Scientific, where you'll make a meaningful impact on global healthcare through our clinical research services. As a Contract Coordinator, you'll play a key role in managing Clinical Trial Agreements (CTAs) with research sites and principal investigators worldwide. Working alongside Contract Analysts, you'll help facilitate critical documentation that enables innovative clinical trials across multiple countries. Your work will directly contribute to advancing therapies while ensuring compliance and efficiency in the contract management process.

This position offers opportunities to build relationships with clinical teams and research sites, manage complex documentation workflows, and contribute to the successful execution of international clinical trials. You'll be part of our mission to make the world healthier, cleaner, and safer while developing your career in a supportive work environment that values work-life balance.

REQUIREMENTS:

  • 1 year of relevant experience in contract administration or similar role

  • Legal background preferred

  • Advanced/fluent English language proficiency with excellent written and verbal communication skills

  • Proficiency in Microsoft Office, particularly Word and Excel

  • Strong understanding of clinical trial agreement processes and documentation

  • Experience with budget preparation and negotiation

  • Demonstrated ability to manage multiple priorities and meet deadlines

  • Excellent organizational skills and attention to detail

  • Ability to work independently while maintaining team collaboration

  • Knowledge of and ability to adhere to SOPs, WPDs, and regulatory requirements

  • Experience with document management systems and electronic signature platforms (e.g., DocuSign)

  • Strong customer service orientation and interpersonal skills

  • Ability to maintain accurate records and databases

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.

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