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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Associate Site Contract Specialist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in MexicoNo 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 accepted as equivalent.
  • Basic understanding of clinical trial agreements is required.
  • Ability to apply basic principles of investigator grant negotiation is required.
  • General understanding of business and financial principles related to service agreements is required.
  • Effective verbal and written communication in English and the local language is required.
  • Working knowledge of PPD standard operating procedures and work practice documents is required.
  • Ability to organize competing priorities logically and review outstanding contractual risks and issues is required.
  • Ability to use automated systems and computerized applications is required.
  • Ability to demonstrate customer-focused communication, problem-solving, and collaboration is required.
  • Ability to work in an upright or stationary position for 6–8 hours per day is required.
  • Ability to make fast, simple, repeated movements of the fingers, hands, and wrists is required.
  • Frequent mobility, occasional crouching and stooping, and frequent bending and twisting of the upper body and neck are required.
  • Ability to lift or carry objects including luggage and a laptop, up to a maximum of 15–20 pounds, is required.
  • Ability to communicate information clearly and understand spoken information is required.
  • Ability to perform variable tasks under stress, multitask, and maintain regular and consistent attendance is required.

Responsibilities

  • Draft, review, negotiate, and finalize amendments and budgets with study sites in accordance with local and accepted processes.
  • Negotiate investigator grant budgets, contractual terms, and conditions within approved parameters and 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 ensure site and study contract negotiation aligns with the critical path for site activation.
  • Achieve target cycle times for site activations.
  • Follow guidelines and processes for efficient escalation of issues 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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