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Posted 1 weeks agoClinica Research Coordinator IV
Roanoke, United StatesOn-site
Responsibilities
- Ensure compliance with study protocol and
Requirements
- Acts as a champion for clinical research at Carilion Clinic. What We Require: Education: Bachelor's degree in science or related field required.
- Master's degree in science or related field preferred.
- Experience: Minimum of ten (10) years of Clinical Research (or equivalent research experience) AND a master's degree in science OR Minimum of fifteen (15) years of Clinical Research (or equivalent research experience) AND a bachelor's degree in science required.
- Licensure, certification, and/or registration: Nationally recognized clinical research certification from Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) required upon hire.
- I.A.T.A. (International Air Transport Association) certification is required for projects that will be transporting specimens prior to completion of IRB application. Other Minimum
- Qualifications: Excellent computer skills; strong knowledge of word processing, spreadsheets, databases, and internet environment.
- Knowledge of medical and/or pharmaceutical terminology strongly desired.
- Must have strong leadership, interpersonal and teamwork skills.
Benefits
- Carilion Clinic is an Equal Opportunity Employer: We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, national origin, age (40 or older), disability, genetic information, or veterans status.
- benefits package, and many perks and well-being resources to help you live a happy, healthy life – at work and when you’re away.
- benefits available to you when you join Carilion: Comprehensive Medical, Dental, & Vision
- Benefits Employer Funded Pension Plan, vested after five years (Voluntary 403B) Paid Time Off (accrued from day one) Onsite fitness studios and discounts to our Carilion Wellness centers Access to our health and wellness app, Virgin Pulse Discounts on childcare Continued education and training
Contact
- The incumbents may be requested to perform job-related tasks other than those stated in this description. Recruiter: RHONDA JOHNSON Recruiter Email: rejohnson@carilionclinic.org For more information, contact the HR Service Center at 1-800-599-2537.
- For more information on E-Verify: https://www.carilionclinic.org/eoe-e-verify-and-right-work-policies Benefits, Pay and Well-being at Carilion Clinic Carilion understands the importance of prioritizing your well-being to help you develop and thrive.
Additional details
- Employment Status: Full time Shift: Day (United States of America) Facility: 101 Elm Ave - Roanoke Requisition Number: R160297 Clinica Research Coordinator IV (Open) How You’ll Help Transform Healthcare: The Clinical Research Coordinator IV Manages administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.
- Serves as liaison between research sponsors, site management organizations, local Institutional Review Board (IRB), physicians/staff, and R&D. The Clinical Research Coordinator IV Manages administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.
- Serves as liaison between research sponsors, site management organizations, local Institutional Review Board (IRB), physicians/staff, and R&D.
- Recruit, screen, and enroll eligible study participants.
- Manages completion and submission of study related documentation.
- Communicates with research sponsor or CRO, local or central IRB, Research and Development, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance.
- Monitors enrollment goals and implements action plans, as needed.
- Coordinates tasks such as developing informed consents and screening materials, scheduling visits, and acting as a liaison between research participants and the research study team.
- Collects data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
- Collect, process, and ship research specimens as directed in the protocol.