Supervisor Clinical Research Position Available In Mecklenburg, North Carolina

Supervisor Clinical Research
STJ – St. Jude Affiliate Clinic
Charlotte, North Carolina
Medical Group
Peds Med Clinic
Full-Time
8:00am-5:00pm
69927
Job Description
Job Summary The team member will act as an agent of the physician investigators and research staff conducting sponsored and independent clinical trials. They will perform and oversee all necessary regulatory, contract, and administrative functions and as specified below. The purpose of the Clinical Research Supervisor is to ensure that studies are adequately maintained in accordance with FDA Regulations, Good Clinical Practice Guidelines, ICH Guidelines and Novant Health policies/procedures. The Clinical Research Supervisor will provide direct leadership for a team of research specialists and coordinators in the department. 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:

4 Year / Bachelors Degree, required. Degree in health science or business.

Experience:

 5+ years of experience in a clinical research setting, required.

Licensure/Certification:

ACRP / SOCRA

/ equivalent, required.
Additional Skills (required):
Proficiency in Microsoft Office and experience with Electronic Medical Record (EMA) systems including Epic, OnCore and eReg.
Proven organizational and communication skills, both oral and written, with the ability to lead and collaborate effectively in a dynamic environment.
Exceptional attention to detail and commitment to research integrity and accuracy. Job Opening ID 69927