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Clinical Research Manager

Job in Cary, Wake County, North Carolina, 27518, USA
Listing for: Gss Anc
Full Time position
Listed on 2026-02-14
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Posted Wednesday, February 4, 2026 at 6:00 AM

Glacier Support Services (GSS), LLC is seeking a qualified Clinical Research Manager gg, NC to provide the following:

Responsibilities
  • Interacts regularly with clinical investigators, clinical site coordinators, regulatory and safety monitoring staff, laboratory personnel, data coordination center personnel, data analysts, biostatisticians, program managers and administrative staff.
  • Coordinates the execution of clinical research proposals, coordination of the proposal submission and scientific/ethical review processes, management of protocol development activities, oversight, and guidance of protocol execution activities at clinical sites, and ensuring project completion and final product development (e.g., presentation and/or publication, recommendations for changes in clinical practice, provision of pivotal data for product licensure).
  • Conducts literature reviews and drafts scientific and technical documents under the direction of clinical investigators and other members of the investigative team.
  • Makes recommendations for process improvements and/or enhancements. Contributes to the design and overall goals of the quality control and quality assurance plan for a study, when needed.
  • Contributes to the development and modifications of study budgets and is responsible for budget compliance and development/tracking of protocol performance metrics.
  • May include budgetary responsibility to include plan/forecast and prepare.
  • Adheres to compliance and privacy/confidentiality requirements and standards, including DOD specific regulations and guidance. Adheres to GCP and compliance regulations for clinical trials.
  • Interview potential participants for clinical trials, collect and analyze data to validate eligibility and subject commitment.
  • Conducts and documents informed consent discussions for subjects and informs them of their rights and responsibilities.
  • Educates participants about the clinical trial, their roles in the protocol and any other vital information. Acts as a research case manager for the subjects. Serves as initial POC for subjects.
  • Collects data appropriately to research protocols. Analyzes data resulting from the tests performed on the subjects. Helps determine whether data is clinically significant. Addresses data queries.
  • Acts as liaison between participants and physicians. Observes the subjects for improvements, setbacks and changes in conditions as required by protocol.
  • Prepares and maintains manual and computerized data in subject study files according to prescribed standards. Administers investigational drugs as specified in protocols.
  • May perform other duties and responsibilities as assigned or directed by the supervisor. This may include attendance of and participation in required training for role.
Qualifications
  • Bachelor’s degree in related area. Advanced degree preferred.
  • 5-7 years of experience with BA/BS or equivalent years of relevant experience in research environment, preferably in DoD, other government agency, or academia.
  • Ability to analyze complex problems involving long and short-range planning, including obtaining sources for data and information, recruitment of subjects, and performing study activities.
  • Excellent interpersonal, organizational, and time management skills.
  • Ability to take initiative and demonstrate strong commitment to duties.
  • Organizational skills to establish effective workload priorities to facilitate multiple programmatic functions such as clinical, research, and administrative.
  • Skill in performing a variety of duties, often changing from one to another with frequent interruptions.
  • Adaptable to quickly changing priorities and situations.
  • Works effectively as a motivator of other employees.
  • Working knowledge of clinical protocol design, content, and categories for inclusion in final document.
  • Demonstrated skills in employee supervision and HR administration.
  • Demonstrated ability to develop and implement plans for evaluation and activation of complex research protocols at new sites.
  • Competent in Microsoft Office (Teams, Outlook, Word, Excel, and PowerPoint).
  • Excellent computer skills required.
Clearance Requirements

Public Trust

GSS offers a competitive benefits package to include: paid holidays, paid time off including sick and vacation leave, medical, dental and vision insurance, flexible spending accounts, short and long term disability, company paid life insurance, 401(k) with a company match and discretionary profit sharing and tuition reimbursement.

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