Overview:
The Clinical Research Specialist is responsible for the coordination, collection, processing and quality control of clinical trial data under the direct supervision of the Manager Clinical Research. Maintains all research protocol data and compliance reporting. Assists with screening patients for research protocol regimens. Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship.
This is more of an entry level role into Clinical Research or for candidates that are interested in provided the administrative support and doing the data work for the Clinical Research team. This is NOT a Coordinator Position. Looking for candidates with some clinical experience such as Lab, CNA, or Medical Assistant as this position may work with lab samples.
Positions are primarily on-site, Monday through Friday. Some positions may offer Hybrid work 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:
Candidates who meet any qualification level outlined below are encouraged to apply!
Clinical Research Specialist I
Clinical Research Specialist II
Clinical Research Specialist III
No experience required. Prefer previous experience in clinical research or healthcare setting such as Lab, billing, coding, insurance, phlebotomy, pharmacy, physician practices
Minimum 5 years* of clinical or clinical research experience required. 2 years must be in clinical research
Minimum 8 years* of clinical or clinical research experience required. 5 years must be in clinical research. Certification in Clinical Research required.**
* Education may count toward years of experience.
** Accepted certifications in Clinical Research include the Association of Clinical Research Professionals (ACRP), the Society of Clinical Research Associates (SOCRA), Regulatory Affairs Professionals Society (RAPS) or Public Responsibility in Medicine and Research (PRIM&R).
* Additional Skills (required):
* Must have exceptional organizational and analytical skills. Self motivated and able to work independently. Able to meet multiple deadlines for concurrent projects. Work in a team-oriented setting. Must have excellent computer skills and medical terminology competency.
* Must provide own transportation to clinics, hospitals and associated agencies as required.
* Manual dexterity, prolonged standing or sitting. Able to lift light to medium weight objects which may be bulky and awkward.
* Ability to travel to developmental, educational and promotional activities.
* Physical and mental stamina required to function effectively in an environment with multiple fluctuating priorities.
* Ability to communicate effectively with individuals of diverse backgrounds and multiple levels of leadership.
* Exposure to hazardous materials (study agents, biohazards, pathology specimens).
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