Description
Make an impact on patient health!
As a Senior 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.
You will 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, Project Management team, and other departments as necessary.
Coupled with reviewing documents for completeness, consistency, and accuracy, under guidance of senior staff, you will prepare site documents, review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.
You will also support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.
Requirements:
- Bachelor’s Degree in Life Science or related field
- Minimum 2 years’ work experience; 1+ years in healthcare or similar
- Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
- Ability to work on multiple projects
Benefits:
- Exposure across 21 Therapeutic Areas
- Be part of a global team who operate across 141 locations
- Exposure across a variety of studies and projects
- Access to new, innovative technologies
- Work within a collaborative and vibrant environment
- Own your career!