Site Activation Specialist (for US sites) in Argentina or Brazil
Site Activation Specialist (for US sites) in Argentina or Brazil
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Job Description
Our Site Activation Specialists work under moderate supervision executing the feasibility site identification regulatory start-up and maintenance activities in accordance with regulations SOPs and project requirements at the regional or country level. You will prepare and manage site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains reviews and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines.
- Serve as a Single Point of Contact (SPOC) to perform feasibility site activation and some maintenance 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
- Review documents for completeness consistency and accuracy under guidance of senior staff
- Prepare site documents reviewing for completeness and accuracy
- Inform team members of completion of regulatory contractual. and other documents for individual sites
- Distribute completed documents to sites and internal project team members
- Update and maintain internal systems databases tracking tools timelines and project plans with accurate and complete project specific information
- Review track and follow up the progress the approval and execution of required documents such as questionnaires CDAs regulatory ethics Informed Consent Form (ICF) and Investigator Pack (IP) release documents
REQUIRED KNOWLEDGE SKILLS AND ABILITIES
- Bachelors Degree in Life Science or related field
- 1 - 3 years prior experience in life sciences or similar (or equivalent combination of education training and clinical healthcare and/or pharma experience) working with regulatory and start up activities is a must. Prior experience supporting US sites is highly valuated.
- Advanced level of English (youll be working with North America on a daily basis)
- Ability to work independently to problem-solve collaboratively and to raise issues appropriately as needed
- Good interpersonal communication and organizational skills to establish and maintain effective working relationships with co-workers managers and sponsors
Home based role in Argentina or Brazil!
#LI-NRJ #LI-Remote
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. Learn more at
Required Experience:
IC
Employment Type
Full-Time
