Clinical Research Coordinator II

Novant Health; Winston-Salem (NC); On-site; USD 60,000 - 85,000; Full time

Job summary

Novant Health seeks a Clinical Research Coordinator to support daily clinical trial activities under the principal investigator. The role emphasizes ethics, safety, quality, and compliance in trial conduct, with independence in handling study tasks and strong communication with staff and patients.

The candidate should have a high school diploma or GED (bachelor's preferred) and at least five years of clinical research experience, plus certification in research (ACRP/SOCRA or equivalent)

Qualifications

• Requires knowledge of complex clinical research concepts gained through education and experience.
• Ability to work with independence and discretion in task execution.
• Strong verbal and written communication skills with patients and staff.
• Ability to meet multiple deadlines and manage multiple protocols.

Skills

Complex clinical research

Independent judgment

Communication

Attention to detail

Time management

Problem solving

Interpersonal skills

Protocol adherence

Education

High School Diploma or GED

Bachelor's degree preferred

Job description

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.

Why Choose Novant Health?

At Novant Health, we believe remarkable care starts with compassion for our patients, our communities, and each other. We value belonging, courage, personal growth, and teamwork, creating a space where everyone is respected, supported, and safe to show up as their full selves.