Director of Clinical Research-CFV Research Institute-Javara, Fulltime Days Position Available In Cumberland, North Carolina

Tallo's Job Summary: The Director of Clinical Research at CFV Research Institute-Javara, located at Cape Fear Valley Medical Center in Fayetteville, NC, is a full-time position with an estimated salary of $42.6K - $53.6K a year. The role requires a Master's degree in healthcare or a relevant field, clinical research certification, 2 years of clinical trial research experience, and supervisory experience. Responsibilities include collaborating with research partners, managing clinical trials, coordinating trial site visits, and ensuring compliance with regulations.

Company:
Cape Fear Valley Health System
Salary:
JobFull-timeOnsite

Job Description

Director of Clinical Research-CFV Research Institute-Javara, Fulltime Days Cape Fear Valley Medical Center – 3.2

Fayetteville, NC Job Details Full-time Estimated:

$42.6K – $53.6K a year 3 days ago Qualifications Clinical research Master’s degree Supervising experience Organizational skills Clinical trials Good Clinical Practice Computer skills Patient interaction Senior level 2 years Communication skills Full Job Description Facility Cape Fear Valley Medical Center Location Fayetteville, North Carolina Department CFV Research Institute_Javara Job Family Management Work Shift Days (United States of America) Summary The Director of Clinical Research will work collaboratively with the Cape Fear Research Institute and their partner(s) established through a Research Collaboration Agreement, the CFV Clinics, CFV Operational and Finance Leadership, and Principal Investigators to conduct clinical trials and research safely and effectively throughout the Health System. This position is responsible for review of potential studies through CFRI, vetting studies collaboratively with the research partner and affected Service Lines, potential principal investigators, coordination of trial site visits and IRB approvals, and assistance with opening and managing all aspects of clinical trial implantation in the CFV Health System. This position is responsible for collaboration with the research partner on coordination of all patients on trials and ensuring all aspects of trial management and clinical requirements are completed according to study. This position is responsible for coordinating administratively with CFRI partner by providing clinical data for data collection and audits. Education responsibilities include presenting information to patients, families, and the community specific to clinical research.

EDUCATION AND FORMAL TRAINING

Master’s degree in healthcare or relevant field required. Clinic research certification from Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) preferred.

KNOWLEDGE, SKILLS, AND PHYSICAL ABILITIES

Minimum 2 years’ experience in clinical trial research including implementation and adherence to study protocols, research participant recruitment, and audit operations related to compliance with applicable regulations. 2-3 years supervisory experience required. Required skills include the ability to communicate effectively with patients, physicians, technicians, and others, provide patient education, and generate appropriate referrals to medical or other clinical resources. Ability to meet physical and mental requirements in a fast-paced, complex ambulatory care setting including verbal communication with patient, families, and staff members, minor lifting, self ambulating, good visual acuity, organizational skills, and computer skills. Demonstrates understanding and requirements of Federal Regulations, GCP, Corporate Compliance, HIPAA, TJC, and Health System and departmental policies and procedures related to Clinical Research. Position may involve skin, eye, mucous membrane, parenteral contact with blood or other potentially infectious material. Required Licenses and Certifications Cape Fear Valley Health System is an Equal Opportunity Employer M/F/Disability/Veteran/Sexual Orientation/Gender Identity

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