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Contract Coordinator

Thermo Fisher Scientific
Posted 17 days ago, valid for 19 days
Location

Wilmington, NC, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The position of Contract Coordinator at Thermo Fisher Scientific requires 1 year of relevant experience in contract administration or a similar role.
  • This role involves managing Clinical Trial Agreements (CTAs) with research sites and principal investigators globally, contributing to the advancement of global healthcare.
  • Candidates should possess advanced English language proficiency, strong communication skills, and proficiency in Microsoft Office, particularly Word and Excel.
  • A legal background is preferred, along with the ability to manage multiple priorities and adhere to regulatory requirements.
  • The job offers a standard Monday to Friday work schedule and emphasizes a supportive work environment that values work-life balance, with a competitive salary based on experience.

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



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