(sr.) Contract Specialist

Trzdev37

Clinical study agreement management
Clinical research coordinator agreement management
Site activation agreements
The Contract Specialist will be responsible for study level contract management, including but not limited to Clinical Study Agreement, Clinical Research Coordinator Agreement and other required agreements mandatory for site activation, as well as their relevant amendments

Job Summary

  • The Contract Specialist will be responsible for study level contract management, including but not limited to Clinical Study Agreement, Clinical Research Coordinator Agreement and other required agreements mandatory for site activation, as well as their relevant amendments.
  • This role will take advantage of Astra Zeneca contract system platform to play a key role during study site start-up stage by driving the contract process, while in the meantime act within the study team as the primary contact point for contract issue including contract quality.
  • AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.

Matching Summary

The Contract Specialist will be responsible for study level contract management, including but not limited to Clinical Study Agreement, Clinical Research Coordinator Agreement and other required agreements mandatory for site activation, as well as their relevant amendments.

Skills & Requirements

Must-have

  • Clinical Study Agreement management
  • Clinical Research Coordinator Agreement management
  • Site activation agreements
  • Contract system platform usage
  • Study team primary contact
  • Contract quality assurance

Nice-to-have

  • Good interpersonal skills
  • Ability to work in an international team
  • Excellent organization and time management
  • Ability to multi-task
  • Team oriented and flexible
  • Respond quickly to shifting demands

Key Requirements

  • Bachelor degree or above
  • At least 3 year industry experience
  • Knowledge of clinical study process
  • Understanding of ICH/GCP guidelines
  • Fluent in both oral and written English
  • Good computer skills in Microsoft

Work Rights

Not specified

Tailored Resume

Cover Letter