Clinical Trials Lead Consultant
A company is looking for a Clinical Trials Lead Consultant. Key Responsibilities: Manage the initiation of research studies, including IRB applications and study setup Identify and screen eligible study participants and develop recruitment materials Create and implement study execution workflows and facilitate stakeholder communication Required Qualifications: Proven experience in clinical trials management or research coordination Strong knowledge of GCP and HIPAA regulations Experience with IRB submissions and contracting processes Master's Degree required; Doctorate Degree preferred Experience conducting oncology or related clinical trials (5 years minimum)
