Site Activation Coordinator
2 months ago
Job Overview
Under general supervision, update systems associated with site activation activities in accordance with the applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.
Essential Functions
- Under general supervision, perform site activation activities in assigned studies, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Update systems and review documents for completeness, consistency and accuracy, under guidance of senior staff.
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 through to completion.
**Qualifications**:
- Bachelor's Degree Life sciences or a related field. Req
- 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Productive individual contributor who works under general supervision. Problems faced are generally routine but may require interpreting procedures or policies to resolve.
- Good interpersonal communication and organizational skills.
- 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.
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