Applicants should submit cover letter and CV/resume to

NCGS Laboratories, Inc.
Department of Human Resources
63 Society Street
Charleston, South Carolina 29401

or

via email to: HR@ncgs.com
with "Employment Opportunities (Position #)" as the subject.
*No phone inquiries please*
Clinical Research Associate Level I Qualification Criteria
  • 1+ years of clinical research experience, either as a research coordinator, monitor, or medical professional
  • A medical science related degree from an accredited university
  • A proven track record of completing detail oriented tasks correctly, meeting deadlines, and employing time management skills effectively
  • Demonstrated ability to take initiative, provide problem solving and trouble shoot in both team and individual situations
  • The ability to establish and maintain positive rapport with medical professionals, clients and team members
  • A willingness to continually apply oneself to learning new skills and obtain knowledge on a variety of medical topics
  • Computer proficiency with MS Word, Excel, and Access
  • Consistent abilities to effectively communicate in a positive manner, in both oral and written formats to enhance team, site and client relations
  • The ablility to travel, nationwide, up to 80% of the work week
  • Ability to complete standard forms, paperwork, and reports associated with research studies, electronically
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Clinical Research Associate Level II Qualification Criteria
  • All of the criteria listed in the CRA, Level I Criteria list
  • 2+ years of clinical monitoring experience on research studies
  • Experience on multiple research studies performing qualifying, initiating, monitoring and close-out visits
  • Demonstrate the ability to provide innovative solutions and display resourcefulness
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Clinical Research Associate Level III Qualification Criteria
  • All of the criteria listed in the CRA, Level I & Level II Criteria Lists
  • 3+ years of clinical monitoring experience on multiple research studies
  • Display the ability to mentor team members and serve as a team lead on projects
  • Demonstrate the ability to learn and fulfill project manager responsibilities occansionally
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Clinical Project Manager Qualification Criteria
  • 3+ years of clinical project management experience, overseeing multiple clinical teams within the research industry
  • A medical science related degree from an accredited university
  • Experience reviewing and managing labor hours within contract requirements effectively
  • A proven track record of effectively managing and mentoring clinical professionals
  • Thorough knowledge of Good Clinical Practices (GCP) and Regulatory (FDA) requirements
  • The ability to establish and maintain excellent relationships with clients
  • The ability to qualify study sites and serve as a monitor occasionally
  • Excellent communication, time management, and organizational skills
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Regulatory Affairs Qualification Criteria
  • 3+ years of relevant experience ensuring compliance on clinical research studies
  • A Bachelor's degree from an accredited university
  • A proven track record of overseeing regulatory affairs for multiple, concurrent research studies
  • The ability to establish and maintain excellent relationships with clients
  • Thorough knowledge of GCP, ICH, IRB, and FDA requirements
  • Excellent communication, time management, and organizational skills
  • Computer proficiency with MS Word, Excel, and Access
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