This job has expired

Clinical Research Coordinator

Virginia Commonwealth University
Virginia, United States
Salary Not Specified
Posted Date
Aug 12, 2021

View more

Position Type
Faculty Positions, Health & Medicine, Medicine, Pediatrics, Surgery, Administrative, Academic Affairs, Research Administration
Employment Type
Full Time
You need to sign in or create an account to save a job.

Position Information

University Code 34111 University Title Clinical Research Coordinator University Job Family Research - Support ORP Eligible No For more information on ORP, visit: Retirement Plans
Recruitment Pool All Applicants Recruitment Type Multi Title Scope of Search Regional Working Title Clinical Research Coordinator Position Number 593660 Is this employee on a H1B Visa? Position Type Staff Job Status Full-Time FLSA Indicator Exempt Employee Group University Employee Department Neurology Organizational Overview

At VCU, we Make it Real through learning, research, creativity, service and discovery — the hallmarks of the VCU experience. A premier, urban, public research university nationally recognized as one of the best employers for diversity, VCU is a great place to work. It’s a place of opportunity, where your success is supported and your career can thrive. VCU offers employees a generous leave package, career paths for advancement, competitive pay, and an opportunity to do mission-driven work.

Position Primary Purpose and General Responsibilities
This position would serve as a coordinator for the Translational Research Program in Muscular Dystrophy. This program is responsible for developing disease modifying and other innovative therapies for individuals with muscular dystrophy. In this role, the individual would work with a group that leads an international network aimed at achieving this objective.
For all clinical research studies assigned, the Clinical Research Coordinator is responsible for coordinating clinical research studies in a compliant and efficient manner. Under the direction of the Principal Investigator (Pl), collaborate will all members of the clinical research team to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and that ethical obligations are kept. Key responsibilities include:
• Demonstrated understanding of clinical research management duties from study initiation to close-out.
• Conduct clinical research activities as authorized by the Principal Investigator’s documented Delegation of Authority and Training Logs.
• Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice ( GCP ), Clinical Research Coordinator, plus additional sponsor GCP certifications as required.
• Understand and adhere to all I RB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols.
• Conduct all assigned activities in compliance with national, local, & institutional guidelines, according to all HIPAA, GCP, and other applicable requirements. Activities include coordinating: new study activation requirements, screening/enrolling participants, regulatory and compliance requirements, maintaining appropriate study documentation/records, and managing study data.
• Provide on-call coverage. Minimum Hiring Standards
Minimum 2 years prior experience. Formal clinical education and experience also required (RN, LPN, CNA, or CMA ) with active license. Ability to work in a diverse environment. Preferred Hiring Standards
Experience in human subjects research with participants with neurological disorders. Clinical Research Coordinator certification is preferred ( CCRC, CCRP, CCRA ). Phlebotomy skills. Familiarity with REDCap database and video editing software. Experience administering validated survey instruments. Required Licenses/ Certifications
RN, LPN, CNA, or CMA with active license Anticipated Hiring Range $45,000 - $70,000 Application Process/Additional Information
We will be recruiting up to TWO positions from this posting Campus MCV Campus Hours/Week 40 Normal Work Days/Hours M-F Job Open Date 08/12/2021 Posting will close on or before Open Until Filled Yes Job Category Research Is this a restricted position? Yes Is this position eligible to participate in alternative work arrangements? No Sensitive Position Yes- A pre-employment fingerprint background check will be required. Resource Critical Yes Quick Link Posting Specific Questions

Required fields are indicated with an asterisk (*).

Optional & Required Documents
Required Documents
  1. Cover Letter/Letter of Application
  2. Resume
Optional Documents

You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert