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Site Contract Associate

82% Flex
EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE - FULLY FLEXIBLE
Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Fluency in English and Portuguese, Bachelor's degree or equivalent experience, Experience in negotiating and writing contracts.

Key responsabilities:

  • Negotiating, finalizing, executing site contracts
  • Ensuring compliance with regulatory requirements
  • Maintaining positive relationships with trial sites
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Parexel Pharmaceuticals XLarge https://www.parexel.com/
10001 Employees
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Job description

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Your missions

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

PAREXEL is in the process of recruiting a Site Contract Associate to work home-based in Spain. This role focuses on legal contracts within the fascinating industry of international Clinical Research, and will support Portugal's Business needs so being fluent in Portuguese is a must.

The Site Contract Associate (“SCA”) is responsible for negotiation with sites, finalization, and execution of all types of site contracts required for site activation. SCA is also responsible for ancillary documents associated to site contracts. Post-site activation, SCA is responsible for negotiation, finalization, and execution of any amendments to the original contracts. The SCA ensures the highest standard of quality of final documents, as well as their compliance with relevant regulatory requirements, guidelines, and respective country’s applicable laws. The SCA ensures that contracts meet needs of both clients and clinical trial sites, protecting best interests of clients and the company (as applicable), while nurturing and maintaining positive relationships with clinical trial sites.

If you have some experience negotiating and writing contracts this is an exciting opportunity to use this knowledge within Clinical Research. You must be fluent in English and Portuguese (Spanish is a plus).

Skills

  • Strong negotiation, diplomacy, team leadership skills, and excellent organizational ability
  • Ability to successfully work in a “virtual” team environment
  • Ability to complete tasks in an accurate, timely manner and effectively manage multiple tasks
  • Effective time management in order to meet daily metrics or team objectives
  • Ability to take initiative, work independently and delegate

Requirements

  • Fluency in written and spoken English and Portuguese.
  • Bachelor's degree in a related field (e.g., law, economics, business, social sciences), equivalent training or industry experience.
  • Experience in negotiating and writing contracts
  • Experience in team coordination

Please submit English CV for consideration

Required profile

Experience

Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Soft Skills

  • verbal-communication-skills