IQVIA

Site Activation Specialist

In short

This role acts as the single point of contact for investigative sites during clinical study start-up and site activation, coordinating with Site Activation Managers, Project Management, and other teams. It is posted by IQVIA, a global clinical research and healthcare intelligence company, for its site activation function. The job involves preparing and tracking regulatory, ethics, and contractual documents, maintaining project databases, and ensuring timelines are met. It requires a bachelor's degree, one year of clinical research experience, and strong knowledge of medical terminology and regulations.

Essential Functions
•Under general supervision, 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. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
•Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
•Prepare site regulatory 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. Ensure monitoring measures are in place and implement contingency plan as needed.
•Inform team members of completion of regulatory and contractual documents for individual sites.
•Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
•Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
•Perform quality control of documents provided by sites.
•May have direct contact with sponsors on specific initiatives.
Qualifications
•Bachelor's Degree in a related field
•1 year clinical research experience. Equivalent combination of education, training and experience.
•In-depth knowledge of clinical systems, procedures, and corporate standards
•Strong knowledge of medical terminology and regulations
•Broad knowledge of clinical research
•Strong knowledge of Microsoft Office and e-mail applications
•Effective communication, organizational, and interpersonal skills
•Ability to work independently and to effectively prioritize tasks
•Ability to manage multiple projects
•Attention to detail
•Ability to establish and maintain effective working relationships with coworkers, managers and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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