Manager, Clinical Research

Responsible for the day to day oversight and management of the assigned Clinical Trials Office and the assigned staff. Manages the daily operations within the Clinical Trials Office and monitors research activity to ensure compliance with Standard Operating Procedures and Good Clinical Practices.

Responsibilities

Oversight and management of the assigned Clinical Trials Office and assigned staff; Manages daily operations within the Clinical Trials Office and monitors research activity to ensure compliance with Standard Operating Procedures and Good Clinical Practices; Oversees assigned study personnel, including orientation, training, documentation of core competencies, certification mandates, safety/responsible conduct of research education, and performance evaluations; Manages the studies and pipeline portfolio of assigned DWG; Obtains and/or maintains clinical research certification; Participates in department specific goals; Complies with Good Clinical Practice and the Code of Federal Regulations; Other duties as assigned

Requirements

Bachelor's degree and 4 years of relevant experience required; Or equivalent combination of education and experience; CCRP - Certified Clinical Research Professional within 1 year required; SOCRA - Certification In Clinical Research within 1 year required

Nice to have

Master's degree; Previous leadership experience; Demonstrated leadership skills and competency; Ability to effectively manage complex research protocols/procedures; Proficiency in medical terminology, clinical research process and applicable regulatory guidelines and standards; Proficiency in managing multiple and competing priorities/demands; Thorough knowledge of and established track record in assuring GCP, Responsible Conduct of Research standards, applicable safety standards, OSHA guidelines throughout study implementation; Fully adheres to applicable safety and/or infection control standards; Exceptional interpersonal, organizational, and time management skills; highly collaborative, promotes teamwork; Ability to build collaboration among research team members, laboratory staff, patients and families, clinical services; Proficient in MS Office (e.g., Word, Excel, PowerPoint), email, internet; High degree of self-motivation; Recognized ability to function independently