What are the responsibilities and job description for the Sennior Clinical Research Coordinator position at JERSEY SHORE UNIVERSITY MEDICAL CENTER?
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At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community.
Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.
The Senior Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, and implementing a compliant study conduct according to all relevant local, federal, and state regulatory requirements and institutional Policies and Standard Operating Procedures. This role carries out the research and works under the general supervision of the principal investigator responsible for the clinical trial(s) to which the role is assigned. This role is responsible for providing coverage and acting as back-up Project Manager for applicable division, as needed. In addition, this role will serve as preceptor and primary trainer for all newly hired Clinical Research Coordinators.
Qualifications:
Education, Knowledge, Skills and Abilities Required:
- BA/BS diploma/degree in science or healthcare field.
- Minimum of 2 years experience in a Clinical Research Coordinator role, or at least 6 years related experience in the field of clinical research.
- Strong attention to detail and customer service focus.
- Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
- Excellent organizational, presentation, documentation and interpersonal skills.
- Excellent written and verbal communication skills.
- Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.
Education, Knowledge, Skills and Abilities Preferred:
- Education on human subject research and GCP.
Licenses and Certifications Preferred:
- SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC).
If you feel that the above description speaks directly to your strengths and capabilities, then please apply today!