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IQVIA Inc is seeking a Regulatory & Start-up Specialist to manage Site Activation activities in compliance with regulations and project guidelines. The role involves serving as a point of contact for investigative sites, ensuring the quality and timely execution of regulatory documents, and supporting project management teams.
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Job Summary
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Matching Summary
Match Score: 75
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IQVIA Inc is seeking a Regulatory & Start-up Specialist to manage Site Activation activities in compliance with regulations and project guidelines. The role involves serving as a point of contact for investigative sites, ensuring the quality and timely execution of regulatory documents, and supporting project management teams.
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Salary
Base: $46,200.00 - $118,600.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
Site Activation activities
Regulatory compliance
Project timelines adherence
Document review and distribution
Investigative site communication
Nice-to-have
Local expertise
Sponsor interaction
Quality control
Key Requirements
2 years clinical research experience
Equivalent combination of education, training and experience