Site Contract Specialist - Brazil

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

This role can be home based anywhere in Brazil.

PPD's mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our dedicated and forward-thinking teams.

We 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.

Discover Impactful Work:

Manages the preparation, discussions and finalization of contracts with investigative sites. Liaises and establishes effective relationships with internal teams.

A day in the Life:

• Drafts, reviews, negotiates and finalizes amendments and budgets with study sites in line with local/accepted process.
• Negotiates within approved parameters both investigator grant budget mediation parameters, contractual terms and conditions in accordance with contractual considerations, client contractual considerations, established process with clients.
• Ensures compliance to established parameters, authority approval, contractual process and client expectations.
• Ensures compliance of budgetary guidance, templates and process.

Keys to Success:

Education

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification.

Experience

• Previous experience that provides the knowledge, skills, and abilities to perform the job
• In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities

• Basic understanding of clinical trial agreements
• General understanding of business and financial principles related to service agreements
• Fluency in English
• Strong attention to detail
• Excellent analytical and decision based thinking
• Good organizational and time management skills