Site Activation Coordinator
About The Position
IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies meaning a vast amount of career development opportunities are available. As Site Activation Coordinator, under general supervision you will perform tasks at a country level associated with site activation activities. These activities will be in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. Your task may also include maintenance activities. Perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Requirements
- Bachelor’s Degree in Life Science or related field preferred
- Minimum 2 years’ work experience
- 1+ years in healthcare or similar considered advantageous
- Fluent/ native language capabilities, including English
- Productive individual contributor who works well under general supervision
- Good interpersonal communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
- Ability to handle change and ambiguity
- Good technology skills and knowledge of MS Office applications
Nice To Haves
- General awareness of the clinical trial environment and drug development process
- Experience working on multiple projects
Responsibilities
- Review documents for completeness, consistency and accuracy, under guidance of senior staff
- Prepare site regulatory documents, reviewing for completeness and accuracy
- 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
- Distribute completed documents to sites and internal project team members
- Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information
Benefits
- Health and welfare benefits
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
