Site Contract Specialist

Employment Type: Full-time Work Schedule: Standard (Mon-Fri) Environmental Conditions: Office

Position Overview

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.

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.

Responsibilities

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 upon timelines.
• Achieve target cycle times for site activations.

Requirements

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.

Company Information

Thermo Fisher Scientific offers employment w[...rest of company information not provided]