Clinical Research Coordinator
4 weeks ago
Responsibilities:
- Provide support, coordination and leadership for research studies that may involve industry sponsored Phase I, II, III and IV clinical trials, drug, biologic, device, government-funded clinical research, and investigator-initiated clinical research.
- Ensure smooth, accurate progress of studies from the planning and approval stages through study completion and post-study closure.
- Recruit and screen study participants and help facilitate continued participation.
- Abstract data from medical records and other sources.
- Identify, document, and assist with Institutional Review Board (IRB) mandated reporting.
- Develop and ensure compliance with study protocols.
- Participate in the planning, development, and budgeting for clinical trials.
Required Qualifications:
- Minimum of 1-2 years clinical experience (cardiovascular experience in a clinical setting preferred)
- Strong interpersonal, written, and verbal communication skills with a history of working collaboratively as part of a team
- Strong attention to detail, demonstrated critical thinking, problem solving and decision-making abilities
- Ability to handle multiple priorities and be results oriented
- Proficiency in MS Office, Outlook, and electronic medical record systems e.g., Epic
Preferred Qualifications:
- Active licensure via Diploma, Associate's, or Bachelor's degree programs in a healthcare-related field; LPN or RN preferred
- Certified Clinical Research Coordinator/Professional (CCRC or CCRP) certification strongly preferred
About Us
Founded over 40 years ago, MHIF is one of the leading non-profit cardiovascular and vascular research and education institutions in the country. We exist to create a world without heart disease and our mission is to improve people's lives through the highest quality cardiovascular research and education. Staffed with over 90 high caliber employees, we conduct cutting-edge clinical research and transformative community research.
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