Job Information
Novant Health Clinical Research Specialist I in Wilmington, North Carolina
Job Summary
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.
Come join a remarkable team where quality care meets quality service, in every dimension, every time.
#JoinTeamAubergine #NovantHealth. Let Novant Health be the destination for your professional growth.
At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities. Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities.
Responsibilities
It is the responsibility of every Novant Health team member to deliver the most remarkable patient experience in every dimension, every time.
Our team members are part of an environment that fosters team work, team member engagement and community involvement.
The successful team member has a commitment to leveraging diversity and inclusion in support of quality care.
All Novant Health team members are responsible for fostering a safe patient environment driven by the principles of "First Do No Harm".
Qualifications
Education: High School or GED required. 4 Year / Bachelors Degree preferred.
Experience: Two years experience in clinical research and/or relevant clinical field preferred.
Licensure/Certification: Two years in a healthcare setting or clinical research (CRA, Regulatory, clinic, CRO, pharma/biotech/device company, or other related experience) preferred.
Additional skills required: 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.
Job Opening ID
49863
