Clinical Research Specialist

6 days ago


Copenhagen, Copenhagen, Denmark IQVIA LLC Full time

About the Role:

As a Clinical Research Specialist - Site Activation and Management at IQVIA, you will play a vital role in ensuring seamless site activation and management processes. This is an excellent opportunity to leverage your expertise in clinical research to drive project success.

Key Responsibilities:

  • Under general supervision, serve as a Single Point of Contact (SPC) for investigative sites, clients, and other departments as necessary, ensuring effective communication and collaboration.
  • Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables, and project timelines.
  • Perform feasibility, site ID, start-up, and site activation activities according to applicable regulations, SOPs, and work instructions.
  • Prepare site documents, reviewing for completeness and accuracy.
  • Ensure accurate completion and maintenance of internal systems, databases, and tracking tools with project-specific information.
  • Review and provide feedback to management on site performance metrics.
  • Review, establish, and agree on project planning and project timelines, ensuring monitoring measures are in place and implementing contingency plans as needed.

Requirements:

  • Bachelor's Degree in Life science or related field (Required).
  • 3 years' clinical research or other relevant experience; or equivalent combination of education, training, and experience.

About Us:

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Salary Range:$60,000 - $80,000 per year



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