Contract Specialist - English & Spanish-

buscojobs Brasil; Mato Grosso; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading medical devices company is looking for a Contract Specialist to manage contracts related to clinical trials. Responsibilities include drafting, reviewing, and finalizing agreements while ensuring compliance. The ideal candidate holds a Bachelor's degree in Law or Science and has experience in clinical trial agreements. This position offers a full-time remote opportunity with an initial 18-month mission and high chances of extension.

Qualificações

• First experience in clinical research and clinical trial agreements.
• Sense of accuracy and precision.
• Proactive and stress-resistant.
• Ability to effectively manage parallel priorities.
• Existing right to work in Europe.

Responsabilidades

• Manage the end-to-end process for clinical trial agreements.
• Ensure compliance throughout the contract process.
• Liaise with site staff and study teams.
• Keep relevant systems up-to-date.

Conhecimentos

Analytical skills

Communication skills

Negotiation skills

Organization

Time management

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