Contract Specialist - FSP dedicated - France

Thermo Fisher Scientific; United States; Remote; USD 55,000 - 95,000; Full time

Job summary

Join a forward-thinking organization where your role as a Site Contract Specialist will make a significant impact on global health. You will be responsible for preparing and negotiating contracts, ensuring compliance with established processes, and collaborating with internal teams to align site startup activities. This exciting position offers the opportunity to work with a dynamic team dedicated to improving clinical trial processes. Enjoy a competitive remuneration package, annual bonuses, and a supportive work culture that emphasizes integrity and innovation. Make a difference in the world of healthcare and advance your career with us!

Benefits

Competitive Remuneration

Annual Incentive Plan Bonus

Healthcare Benefits

Career Development Prospects

Qualifications

• Bachelor's degree or equivalent with 2-5 years of relevant experience.
• Strong understanding of contract law and negotiation principles.

Responsibilities

• Drafts, reviews, negotiates, and finalizes contracts with study sites.
• Ensures compliance with budgetary guidance and contractual processes.
• Identifies and assesses legal and operational risks in contracts.

Skills

Contract Law Principles

Investigator Grant Negotiation

Interpersonal Skills

Analytical Thinking

Attention to Detail

Organizational Skills

Problem-Solving Skills

Time Management

Education

Bachelor's Degree or Equivalent

Tools

Microsoft Outlook

Microsoft Excel

Microsoft Word

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

Our determined teams combine and deliver startup activities for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our sites, businesses and colleagues around the world to decrease startup timelines and go above and beyond.

Discover Impactful Work:

As a Site Contract Specialist, you will prepare and negotiate contracts, as well as finalize the contract process.

A Day in the Life:

• Drafts, reviews, negotiates and finalizes agreements with study sites in accordance with local/accepted process.
• Negotiates within approved parameters both investigator grant budget negotiation parameters, contractual terms and conditions in per company contractual considerations, client contractual considerations, established process with sites and follows established escalation routes.
• Ensures compliance to established negotiation parameters, authority approval, contractual process and client expectations.
• Ensures compliance of budgetary guidance, templates and process.
• Identifies and assesses legal, financial and operational risks and brings up to appropriate level of the organization per established processes.
• Provides recommendations and alternative resolutions to Investigator Contract negotiations through established escalation channels.
• Coordinates with internal functional departments to ensure various site startup activities are aligned with contractual activities and mutually agreed up timelines.
• Achieve target cycle times for site activations.

Keys to Success:

Education and Experience:

Bachelor's degree or equivalent and relevant formal academic/vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2-5 years’) or equivalent combination of education, training, & experience.

Knowledge, Skills, Abilities:

• Understanding of the principles of contract law, including a general understanding of laws that influence contract language, such as business, intellectual property and local tax and stamp laws.
• Proven ability to apply basic principles of investigator grant negotiation.
• Effective interpersonal skills (verbal and written) in English and in language spoken at local place of work.
• Capable, with appropriate oversight, of drafting and negotiating contract provisions and budgetary issues within parameters.
• Strong attention to detail.
• Excellent analytical and decision-based thinking.
• Understanding of the pharmaceutical product development process and involvement of CROs.
• Able to work independently or in a team environment.
• Good organizational and time management skills.
• Able to organize competing priorities logically and review outstanding contractual risk and issues.
• Able to effectively use automated systems and computerized applications, such as Microsoft Outlook, Excel, Word, etc.
• Ability to demonstrate problem-solving and teamwork skills.

Benefits:

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!