Job Title
Responsibilities and Duties:- In collaboration with the Director of Clinical Trials, support the study operational strategies
- Assist with budget monitoring including invoicing and confirmation of site payments
- Develop meeting agendas, minutes and track follow-up actions
- Ensure eTMF oversight including routine quality checks to maintain a complete and inspection-ready state
- Maintain a vendor and site contact list
- Work with the clinical operations team to maintain clinical trial scorecards for routine review
- Assist clinical sites with questions and resolve queries
- With oversight from the Director Clinical Trials, provide support to the multifunctional team on special initiatives as needed
- Create and improve upon business processes to ensure successful growth
- Knowledge and Experience:
Minimum of 3 years prior experience as a Clinical Research Coordinator is required.
Biological Science degree or Clinical Experience
Will consider other Degrees with a minimum of 4 years equivalent experience as a Clinical Research Coordinator
Minimum 3 years of Oncology experienceBA/BS in a clinical or scientific discipline; Multitasking ability to oversee a large number of projects and reach milestones on time
Strong written and oral communication skills with incredible attention to detail
Willingness to roll up your sleeves and get in the weeds of projects as a jack of all trades
Ability to think outside of the box and challenge the status quo
Natural entrepreneurial spirit with unrelenting dedication to delivering results
Desire to work in a fast-paced, innovative environment
Natural collaborator who enjoys working on a cross-functional team
Domestic travel is required
