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Clinical Trial Operations Opportunities at Parexel

Clinical Trial Operations

Site Contract Leader

Job ID 63743BR USA - Southeast - Home Based
The main responsibility of the Site Contract Leader is managing the entire Clinical Site Agreement (CSA) process for a number of projects, including the development of the study specific CSA strategy with the Sponsor, preparation of the corresponding country specific CSA templates and country specific budgets and also negotiation of such CSA's and budgets with the individual sites located in his/her region/country. Further, the responsibilities include managing CSA activities and liaising with Project Lead, Clinical Operations Lead and the Sponsor to ensure that the CSA start-up deliverables are met.

Qualifications

Possess strong negotiation, diplomacy, team leadership skills and excellent organizational ability
  • Possess excellent interpersonal, verbal and written communication skills
  • Able to motivate both individuals and a team
  • Able to successfully work in a "virtual" team environment
  • Able 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
  • Demonstrate commitment to and performs consistently high quality work
  • Able to identify and address issues proactively
  • Able to take initiative, work independently and delegate
  • Accountable for all assigned tasks
  • Education
    • Educated to the degree level (life sciences, pharmacy, biology, law degree)

EEO Disclaimer

Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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