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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Associate Site Contract Specialist

Clinical Research OperationsPosted on Nov 13
Full-timeRemote in BrazilNo salary listedRemote

About the Job

Requirements

  • A bachelor's degree or equivalent and relevant formal academic or vocational qualification is required.
  • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to 0–2 years, is required; an appropriate combination of education, training, and directly related experience may be considered equivalent.
  • A basic understanding of clinical trial agreements is required.
  • The ability to apply basic principles of investigator grant negotiation is required.
  • A general understanding of business and financial principles related to service agreements is required.
  • Effective verbal and written communication skills in English and the local language are required.
  • Working knowledge of PPD standard operating procedures and work practice documents is required.
  • The ability to organize competing priorities logically and review outstanding contractual risks and issues is required.
  • The ability to use automated systems and computerized applications is required.
  • The ability to communicate in a customer-focused manner when problem-solving and collaborating is required.
  • The ability to work independently or in a team environment is required.
  • The ability to access and use a variety of in-house and off-the-shelf computer software is required.
  • The ability to communicate information clearly, listen to and understand spoken information, and interact frequently with diverse groups is required.
  • The ability to perform under stress, multitask, and maintain regular and consistent attendance is required.
  • The position requires remaining upright or stationary for 6–8 hours per day, repetitive hand and finger movements, frequent mobility, occasional crouching and stooping, frequent bending and upper-body and neck twisting, and light to moderate lifting and carrying up to 15–20 pounds.

Responsibilities

  • Draft, review, negotiate, and finalize amendments and budgets with study sites in accordance with local and accepted processes.
  • Negotiate within approved investigator grant budget parameters and contractual terms and conditions, in accordance with contractual and client considerations and established processes; follow established escalation routes.
  • Ensure compliance with negotiation parameters, approval authority, contractual processes, client expectations, budgetary guidance, templates, and processes.
  • Coordinate with internal functional departments to align site startup activities with contractual activities and mutually agreed timelines, and align contract negotiations with the site and study critical path for site activation.
  • Achieve target cycle times for site activations.
  • Follow guidelines and processes for efficient escalation of issues that fall outside approved parameters, as applicable.
  • Complete required tracking and reporting, and assist other specialists with tracking and reporting.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

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