Clinical Site Activation Coordinator

IQVIA

Durham (NC)

Hybrid

USD 49,000 - 123,000

Full time

14 days+

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Job summary

IQVIA LLC in Durham, NC is seeking a Site Activation Specialist to manage feasibility, site activation, regulatory start-up and maintenance activities across studies. You will coordinate with the Site Activation Manager, project teams and investigative sites to ensure timely and compliant site documentation and contract execution.

The role requires reviewing documents, tracking progress, and maintaining project plans with emphasis on accuracy, regulatory compliance and timely communication with

Qualifications

  • Bachelor's Degree required.
  • 1-3 years’ clinical research or related experience; or equivalent combination of education, training and experience.
  • 3 years’ experience in a healthcare environment or equivalent combination of education, training and experience.

Responsibilities

  • Serve as SPOC to perform feasibility, site activation and some maintenance activities in assigned studies.
  • Review documents for completeness, consistency and accuracy under guidance of senior staff.
  • Prepare site documents and review for completeness and accuracy.
  • Inform team members of completion of regulatory, contractual and other documents for individual sites.
  • Update and maintain internal systems, databases, tracking tools, timelines and project plans.
  • Review, track and follow up on progress, approval and execution of required documents (ICF, CDAs, IP release).

Education

Bachelor's Degree Life sciences or a related field

Job description

IQVIA LLC in Durham, NC is seeking a Site Activation Specialist to manage feasibility, site activation, regulatory start-up and maintenance activities across studies. You will coordinate with the Site Activation Manager, project teams and investigative sites to ensure timely and compliant site documentation and contract execution.

The role requires reviewing documents, tracking progress, and maintaining project plans with emphasis on accuracy, regulatory compliance and timely communication with

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