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Contract Specialist - English & Spanish-

buscojobs Brasil

Mato Grosso do Sul

Teletrabalho

BRL 80.000 - 120.000

Tempo integral

Hoje
Torna-te num dos primeiros candidatos

Resumo da oferta

A leading recruitment platform is seeking a Contract Specialist for remote contract management focused on clinical trial agreements. Ideal candidates will have a Bachelor's degree in Law or Science and experience in clinical research. Responsibilities include managing contract processes and liaising with various departments. This is a full-time, long-term role with significant opportunities for growth.

Serviços

Long-term contract with high chance of extension
Flexibility of remote work

Qualificações

  • Experience in clinical research and clinical trial agreements in the US.
  • Sense of accuracy and precision.
  • Pro-active and stress-resistant.

Responsabilidades

  • Handle the end-to-end process related to clinical trial agreements.
  • Ensure compliance throughout the process.
  • Liaise with site staff, study team, Legal, and Finance.

Conhecimentos

Analytical skills
Communication skills
Negotiation skills
Organization skills
Time management skills

Formação académica

Bachelor’s degree in Law or Science
Descrição da oferta de emprego

THIS IS A ROLE FOR SOMEONE OPEN TO WORK AS A CONSULTANT FREELANCER LONG TERM FOR TOP PLAYER IN MEDICAL DEVICES.

Do you have a first experience in contracting activities for clinical trials ? Are you enthusiastic about clinical trial contracts, budgeting and site negotiation ? You like working in a dynamic, international environment where your strong analytical and communication skills will be of good use? Then this may be the opportunity for you.

Job Description

The Contract Specialist is responsible for contract management, including all operational and administrative functions of the contract. Focus is mainly on clinical trial agreements.

Responsibilities
  • Handle the end-to-end process related to clinical trial agreements (draft, review, negotiation, finalization).
  • Ensure compliance throughout the process
  • Liaise with site staff, study team, Legal and Finance departments
  • Keep relevant systems up-to-date
Requirements
  • Bachelor’s degree in Law or Science
  • A first experience in clinical research and clinical trial agreements in US
  • Sense of accuracy and precision
  • Pro-active
  • Stress-resistant
  • Strong communication and negotiation skills
  • Strong organization and time management skills
  • Ability to effectively manage parallel priorities
  • The existing right to work in Europe
Benefits
  • Fulltime, remote position
  • 18 months mission with high chance of extension
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