Site Activation Manager

5 hours ago


Fatih, Istanbul, Turkey IQVIA Full time
Job Description

In this critical role, you will serve as a single point of contact for assigned clinical studies, managing relationships with investigative sites and internal stakeholders.

Responsibilities Include:
  1. Ensuring Compliance with regulations, SOPs, and WIs, evaluating and improving processes as needed.
  2. Negotiating Contracts and Budgets with sites, coordinating project planning and timelines.
  3. Preparing Site Regulatory Documents, reviewing for completeness and accuracy.
  4. Maintaining Internal Systems and Databases, accurately completing and updating project-specific information.
  5. Collaborating with Cross-Functional Teams, including RSU leads and project teams, on initial and ongoing project planning.


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