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Clinical Research Manager
Job in
Cary, Wake County, North Carolina, 27518, USA
Listed on 2026-02-14
Listing for:
Gss Anc
Full Time
position Listed on 2026-02-14
Job specializations:
-
Science
Clinical Research
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.
- 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.
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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