Contract Specialist - English & Spanish-

buscojobs Brasil; Acre; Teletrabalho; BRL 100.000 - 130.000; Tempo integral

Resumo da oferta

A global medical device company is looking for a Contract Specialist to manage clinical trial agreements. Responsibilities include handling the end-to-end contract process, ensuring compliance, and liaising with multiple stakeholders. Candidates should hold a Bachelor's degree in Law or Science and have a relevant first experience in clinical research. This is a full-time remote position with an initial 18-month mission and a high chance of extension.

Serviços

Fulltime remote position

18 months mission with a chance of extension

Qualificações

• First experience in clinical research and clinical trial agreements in the US.
• Sense of accuracy and precision is essential.
• Pro-active and stress-resistant.

Responsabilidades

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

Conhecimentos

Analytical thinking

Communication skills

Negotiation skills

Organization skills

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