Site Activation Coordinator

IQVIA is hiring a Site Activation Coordinator to perform country-level site activation activities for clinical studies in accordance with regulations, SOPs, and project requirements. The role involves preparing and reviewing site regulatory documents, coordinating their completion and distribution, and maintaining project systems and tracking tools.

Responsibilities

• Under general supervision, 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. Review documents for completeness, consistency and accuracy, under guidance of senior staff
• Prepare site regulatory documents, reviewing for completeness and accuracy
• Inform team members of completion of regulatory and contractual documents for individual sites
• 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
• 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

Preferred

• Bachelor's Degree Life sciences or a related field
• Bachelor's Degree
• Life Sciences

Benefits

• Remote work.
• Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered.
• Dependent on the position offered, a range of health and welfare and/or other benefits may be offered.

Company

• AI-powered talent hiring platform for life sciences, pharma, and IT
• London, England, GBR
• https://lifelancer.com/
• Founded in 2020
• 11-50 employees

Qualifications

• 1 years' experience in a healthcare environment or equivalent combination of education, training and experience
• Good interpersonal communication and organizational skills
• Good word processing skills and knowledge of MS Office applications
• Good attention to detail
• General awareness clinical trial environment and drug development process
• Ability to work on multiple projects
• Ability to establish and maintain effective working relationships with co-workers, managers and sponsors
• Bachelor's Degree Life sciences or a related field
• 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience.

Required skills

• Clinical Trials, Drug Development

Preferred skills

• Bachelor's Degree Life sciences or a related field

Experience

• 1+ years