Temporary Clinical Research Coordinator Certificate Trainee - WV Clinical & Tran

Job Description - Temporary Clinical Research Coordinator Certificate Trainee - WV Clinical & Translational Science Institute (24063) The West Virginia Clinical & Translational Science Institute (WVCTSI) at West Virginia University is currently accepting applications for a Temporary Clinical Research Coordinator Certificate Trainee. About the Opportunity As a Clinical Research Coordinator Certificate Trainee, you will be enrolled in the IDeA State Consortium for Clinical Research – Resource Center (ISOCRE-RC) Clinical Research Coordinator Development Program (CRCDP). Under the supervision of a preceptor, the trainee will complete 400 hours of experiential training and approximately 60 hours of self-paced didactic learning. This program is designed to provide trainees with the basic skills and knowledge to begin a career as a clinical research coordinator or specialist. The goal of the program is to build workforce capacity for clinical trials research. Under direct supervision, trainees will participate in the development, coordination, and implementation of research and administrative strategies essential to the successful management of Phase II/III/IV clinical trials research conducted by faculty at West Virginia University Health Sciences Center. What you’ll do: I. Protocol Compliance: Facilitates compliance with the requirements of the research protocol and good clinical research practice. Identifies the requirements of various types and phases of clinical trials. Promotes compliance with the varied processes and procedures required by different types of sponsors. Protects patient, protocol, and scientific confidentiality. Collaborates with the research team to implement procedures for maintaining patient study participation. II. Clinical Trials–Related Communication: Participates in ongoing communication regarding clinical trials with team members. Provides clinical research information to research, clinical, and other organizational staff. Participates in study initiation meetings. III. Informed Consent Process: Ensures the initial and ongoing consent process is performed and documented. Participates in the education of clinical trial patients. IV. Management of Clinical Trial Patients: Collaborates with the investigator to ascertain study patient eligibility. Assists with the adherence to the protocol schedule of events. Assists with the successful completion of correlative components of the clinical trial. V. Documentation: Complies with regulations, institutional policies, and sponsor requirements governing source data and documentation. Documents assessment, management, and evaluation in source documents. VI. Patient Recruitment: Assists in implementation of recruitment plans. VII. Ethical Issues: Advocates for ethical care of clinical trial patients. Promotes ongoing compliance with key ethical concepts. VIII. Financial Implications: Assists with identifying the financial variables that affect research. IX. Professional Development: Participates in educational opportunities to increase knowledge about clinical trials. Qualifications: Bachelor's degree, or an equivalent combination of education and experience. 0-6 months of related experience. Must possess and apply knowledge of many different and unrelated processes and methods. Skilled at communicating effectively in writing. Ability to develop constructive and cooperative working relationships. Requirements: Medical Monitoring -- This position may or may not require Medical Monitoring. About WVU: At West Virginia University, we leverage our talents and resources to create a better future for our state and the world. Creating an inclusive, engaged, and dynamic learning environment is core to WVU’s academic mission. West Virginia University is proud to be an Equal Opportunity employer and invites applications from all qualified applicants.

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