Clinical Research Nurse

Bristol Bay Native Corportation • Fort Bragg, NC

1d

About The Position

Glacier Support Services (GSS), LLC is seeking a qualified Clinical Research Nurse at Ft. Bragg, NC to provide the following: Responsibilities: Educates subjects on research protocols, purposes of the research, procedures, and subject responsibilities. Answers questions and discusses risks and benefits of participation. Explains and obtains informed consent. Collects data appropriate to research protocols. Documents in medical/research records and on case report forms. Provides subject care including screening, evaluating, and monitoring of subjects. Prepares subjects for office visits and investigational research procedures. Administers investigational product(s). Assists in responding to medical emergencies. Collects, measures, weighs, and ensures safe handling, delivery, and/or transport of various biological samples in accordance with prescribed protocols. Provides feedback to the Principal Investigator to monitor the overall conduct of clinical trials, to include subject care and other issues that may affect subject safety, protocol adherence, and/or program operations. Develops reports and presents clinical results at local and national meetings. Assists in the preparation of research articles for publication in scientific journals. Supports the development of research grants and proposals. May perform other duties and responsibilities as assigned or directed by the supervisor, to include those needed to maintain overall clinical study operations. This may include attendance of and participation in required training for the role. Knowledgeable and proficient with the content of protocols. Identifies problems in research designs or analysis methodologies and trends in subject reactions to treatment. Collects, organizes, catalogs, disseminates, and maintains appropriate files of current data. Assists in the development of research questions, designs, and methodologies. Assists in writing and/or editing protocols and study-related materials.

Requirements

• LPN or RN.
• Certified in basic cardiac life support.
• Clinical studies experience required.
• Phlebotomy skills required.
• Excellent interpersonal skills required.
• Collegiality in team environment.
• Demonstrated ability to work collaboratively and independently.
• Competent in Microsoft Office (Teams, Outlook, Word, Excel, and PowerPoint).
• Possesses interpersonal skills necessary to work effectively with subjects and other staff members.
• Strong oral and written communication skills.
• Ability to think critically.
• Ability to take direction and establish priorities for accomplishment of work assigned.
• Clearance Requirements: Public Trust

Nice To Haves

• Bachelor's Degree in nursing preferred.
• Previous experience working in military/DoD environment, preferably within immunizations, preferred.
• Demonstrated experience in regulatory and IRB submission functions, such as reporting adverse events, and continuing review report submissions.
• Experience with recruiting and enrolling clinical study subjects.

Responsibilities

• Educates subjects on research protocols, purposes of the research, procedures, and subject responsibilities.
• Answers questions and discusses risks and benefits of participation.
• Explains and obtains informed consent.
• Collects data appropriate to research protocols.
• Documents in medical/research records and on case report forms.
• Provides subject care including screening, evaluating, and monitoring of subjects.
• Prepares subjects for office visits and investigational research procedures.
• Administers investigational product(s).
• Assists in responding to medical emergencies.
• Collects, measures, weighs, and ensures safe handling, delivery, and/or transport of various biological samples in accordance with prescribed protocols.
• Provides feedback to the Principal Investigator to monitor the overall conduct of clinical trials, to include subject care and other issues that may affect subject safety, protocol adherence, and/or program operations.
• Develops reports and presents clinical results at local and national meetings.
• Assists in the preparation of research articles for publication in scientific journals.
• Supports the development of research grants and proposals.
• May perform other duties and responsibilities as assigned or directed by the supervisor, to include those needed to maintain overall clinical study operations. This may include attendance of and participation in required training for the role.
• Knowledgeable and proficient with the content of protocols.
• Identifies problems in research designs or analysis methodologies and trends in subject reactions to treatment.
• Collects, organizes, catalogs, disseminates, and maintains appropriate files of current data.
• Assists in the development of research questions, designs, and methodologies.
• Assists in writing and/or editing protocols and study-related materials.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree