Job Description:
• Represents and leads the study team to design, develop and deliver the clinical study to agree upon timelines
• Leads planning and communication with cross-functional teams to ensure proper execution and conduct of the clinical trial
• Serves as primary contact and resource for CRO and vendor personnel in overarching functions
• Provides oversight and management of CROs, consultants and vendors
• Monitors progress of clinical activity and reports on the progress of assigned clinical trials including budget and timelines
• Prepares potential investigator site lists and assists with their evaluation for inclusion in the study
• Participates in meetings – i.e. Study Team Meetings, Investigator Meetings, Monitors’ workshops and CRO Training
Requirements:
• Bachelor’s degree in a related field required
• M.S./Ph.D. in a related life science discipline is preferred
• Minimum of 3-5 years of industry experience in clinical drug or program development or equivalent academic experience in clinical trials
• Strong experience facilitating project team meetings, cross-functional communication and decision making
• Familiarity with the design and conduct of clinical trials and project management in relevant therapeutic areas
• Strong analytical skills with a data driven approach to planning, executing, and problem solving
• Working knowledge of current global regulatory requirements and guidelines for clinical trials
Benefits:
• merit-based salary increases
• short incentive plan participation
• eligibility for our 401(k) plan
• medical, dental, vision, life and disability insurances
• flexible paid time off
• 11 paid holidays plus additional time off for a shut-down period during the last week of December
• 80 hours of paid sick time upon hire and each year thereafter
Apply Now
Apply Now