What are the responsibilities and job description for the Clinical Trial Associate position at Dragonfly Therapeutics?
Clinical Trial Associate
Dragonfly Therapeutics is seeking a highly motivated and experienced Clinical Trial Associate to provide administrative and operational support to Clinical Operations. In this role you will report to a Senior Clinical Trial Manager in Clinical Operations.
Responsibilities:
- Organize, participate in, and maintain agendas and meeting minutes for all internal Clinical Development and cross-functional team meetings. Review external meeting minutes as required
- Work closely with the assigned Clinical Trial Managers to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews)
- Update and maintain internal trackers (e.g. central enrollment tracker, investigator engagement tracker, bioanalytical sample tracker) and implement updates into ad-hoc presentations and reports as required
- Maintain internal Clinical Operations study files and perform periodic reconciliations of documents to ensure all material is present and versioned correctly
- Create and maintain study personnel contact lists for all studies and KOLs by disease indication
- Assist with the review of study-related documents for clinical studies (e.g. protocol, IB, ICFs)
- Assist Senior CTA with the facilitation of important external meetings (e.g. Clinical Advisory Board meetings): outreach, scheduling, execution of CDAs and contracts, travel arrangements, presentations, agendas, and minutes
- Assist Senior CTA with bioanalytical sample tracking and management of central and third-party labs (sample shipment and analysis timelines)
- Assist Senior CTA with the review of central and third-party lab documents (e.g. Lab Manual, site flowcharts)
Qualifications:
- Relevant education and training required; Bachelor’s degree in administrative, science or medical areas of study is a plus
- Experience with oncology clinical trials is a plus
- At least 1 year of successful administrative experience in biotech/life sciences, health care or clinical study management
- Prefers to contribute as both independent, self-starter, and a collaborative team member
- Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment
- Excellent verbal and written communication skills
- Excellent computer skills, including Microsoft Office Suite: Calendar, Word, Excel, and PowerPoint are essential