Clinical Research Coordinator II

Experience : Minimum 5 years of clinical research experience, required (CRA, Regulatory, clinic, CRO, pharma/biotech/device company, or other related) OR Associate's degree may substitute for 1 year of experience OR Bachelor's degree may substitute for 2 years of experience; Master's degree may substitute for 3 years of experience. Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects Training, and International Air Transportation Association (IATA) certification for shipping hazardous and biological substances.

What We Offer:

The Clinical Research Coordinator (CRC) is a clinical research professional working under the direction of their Novant Health leader and the principal investigator. Clinical research coordinators facilitate and coordinate the daily clinical trial activities and play a critical role in the conduct of the study.Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, qualify and compliance.

What We're Looking For:

• Education: High School Diploma or GED, required. 4 Year / Bachelors Degree, preferred. 
• Experience: Minimum 5 years of clinical research experience, required (CRA, Regulatory, clinic, CRO, pharma/biotech/device company, or other related) OR Associate's degree may substitute for 1 year of experience OR Bachelor's degree may substitute for 2 years of experience; Master's degree may substitute for 3 years of experience.
• Licensure/Certification: Professional certification in research; Certification required (ACRP/SOCRA or equivalent), preferred. 
• Additional Skills (required): 
  • Requires demonstrated knowledge of complex clinical research concepts gained through education and experience. Works with a high degree of independence, using discretion and independent judgment in the execution of tasks.
  • Human relations and interpersonal skills necessary for interacting patients and staff.
  • Attention to detail and accuracy necessary. Ability and willingness to work irregular hours as necessitated by research protocols. Excellent verbal and written communication skills. Excellent telephone diplomacy. Working knowledge of Information Systems and database management. Excellent analytical and time management skills. Self-motivated and able to work independently as well as a team. Ability to prioritize and problem solving skills, with demonstrated competency in applying clinical knowledge to patient management. Able to meet multiple deadlines for concurrent projects. Knowledge and assessment skills to provide age appropriate care and protocol requirements.
• Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects Training, and International Air Transportation Association (IATA) certification for shipping hazardous and biological substances.