Research Coordinator – BLES

Jobtailor

Fort Bragg (NC)

On-site

USD 55,000 - 80,000

Full time

14 days+

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Job summary

Jobtailor in the United States is seeking a Research Coordinator to support study execution and data collection in collaboration with a research team. The role emphasizes maintaining safety and confidentiality of participants and adhering to GCP/GLP and CFR guidelines.

The position requires a Bachelor’s degree or equivalent experience, 2–4 years of clinical research or healthcare-related work, and strong communication with diverse stakeholders.

Qualifications

Bachelor’s degree or equivalent work experience required.
U.S. Citizenship required.
Research coordination and data collection experience highly desired.
2-4 years’ experience in clinical research preferred.
2-4 years’ non-profit, research, or healthcare experience desired.
Demonstrate competence in oral and written communication.
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor.
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner.
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines.

Responsibilities

Assist with report generation and project close-out support
Perform data collection responsibilities as assigned
Promote safety and confidentiality of research participants at all times
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives
Document all correspondence and communication pertinent to the research
Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization

Skills

Research Coordination

Data Collection

Data Analysis

Report Generation

Project Close-Out

Research Protocol

Infection Control

GCP Knowledge

GLP Knowledge

CFR Knowledge

ICH Guidelines

Communication Skills

Organizational Skills

Attention to Detail

Diplomatic Communication

Education

Bachelor's degree or equivalent

Tools

Excel

Microsoft Office

Job description

Assist with report generation and project close-out support
Perform data collection responsibilities as assigned
Promote safety and confidentiality of research participants at all times
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives
Document all correspondence and communication pertinent to the research
Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization

Requirements

Bachelor’s degree or equivalent work experience required
U.S. Citizenship required
Research coordination and data collection experience highly desired
2-4 years’ experience in clinical research preferred
2-4 years’ non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines

Core Competencies

Demonstrates expertise in research coordination, data collection, and adherence to regulatory guidelines such as OSHA, GCP, and GLP. Proficient in managing research protocols and effectively communicating with diverse stakeholders.

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