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Site Contract Associate
hace 2 meses
About the Role
Parexel is seeking a highly skilled Site Contract Associate to join our team in Spain. As a key member of our Clinical Research team, you will be responsible for negotiating and finalizing site contracts, ensuring compliance with regulatory requirements and company policies.
Key Responsibilities
- Negotiate and finalize site contracts, including ancillary documents, to ensure compliance with regulatory requirements and company policies.
- Work closely with clinical trial sites to understand their needs and ensure contracts meet their requirements.
- Develop and maintain positive relationships with clinical trial sites, ensuring a high level of customer satisfaction.
- Collaborate with internal stakeholders to ensure contracts meet business needs and protect company interests.
- Stay up-to-date with regulatory requirements and industry developments to ensure compliance and best practices.
Requirements
- Fluency in written and spoken English and Portuguese.
- Bachelor's degree in a related field, such as law, economics, business, or social sciences.
- Experience in negotiating and writing contracts, preferably in the pharmaceutical or clinical research industry.
- Strong negotiation, diplomacy, and team leadership skills.
- Ability to work independently and as part of a virtual team.
What We Offer
Parexel offers a dynamic and challenging work environment, with opportunities for professional growth and development. As a Site Contract Associate, you will have the opportunity to work with a talented team of professionals, contribute to the success of our clients, and make a meaningful impact in the clinical research industry.
