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Research Coordinator

The Geneva Foundation·Colorado Springs, Colorado

$60,000 - $65,000/yr·Part Time·On Site·Remote friendly·2-5 yrs
·Posted 2 months ago
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About the role

The Research Coordinator oversees and administers research study activities, including project planning, regulatory compliance, and protocol implementation. They also manage data collection systems, recruit research subjects, and coordinate technical support staff to ensure study objectives are met.

About the Position

The Research Coordinator I oversees and administers research study and associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed. May recruit and coordinate research subjects, as appropriate, and serves as principle administration liaison for the project. Oversees and coordinates the provision of administrative and staff services to investigators; develops and maintains record keeping systems and procedures.

About the Project

This position will support multiple research projects under the MIRROR program.

Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) delivers high value research, education, training, and infrastructure for over 40 clinically relevant musculoskeletal injury (MSI) studies within the military health system (MHS).

MIRROR supports a broad scope of projects, including epidemiological investigation, investigator initiated pilots, and prospective randomized multisite clinical trials.

Areas of clinical evaluation comprise general MSI care process models and highly prevalent anatomically-specific (e.g. back, knee, shoulder pain, etc.) targeted interventions with protocols examining effective return-to-duty activities.

These studies particularly focus on deployment-limiting MSIs, ensuring that research addresses the challenges faced by service members in maintaining operational readiness.

Results of these studies generate evidence-based approaches for future clinical practice guidelines as well as educational opportunities for future military and civilian providers at WRNMMC and USU.

Compensation: $30,000

Qualifications

  • Bachelor’s degree or equivalent work experience required
  • 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

  • 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

Candidates must possess a bachelor's degree or equivalent experience, with 2-4 years of experience in clinical research or healthcare preferred. Proficiency in Microsoft Office, knowledge of regulatory guidelines (CFR, GCP, ICH), and strong organizational and communication skills are required.

  • bachelor degree
  • Communication
  • Microsoft Office
  • Microsoft Excel
  • Record keeping
  • Infection control
  • Regulatory compliance
  • Data analysis
  • OSHA compliance
  • Project planning
  • Data collection
  • Clinical research
  • Protocol implementation
  • ICH guidelines
  • Subject recruitment
  • GCP guidelines
  • CFR guidelines

Benefits

  • Dental insurance
  • Vision insurance
  • Medical insurance
  • Paid holidays
  • Paid time off
  • Short-term disability
  • Long-term disability
  • Life insurance
  • Employee assistance program
  • Flexible spending account
  • Health savings account
  • Accidental death and dismemberment insurance
  • Employer match
  • Public service loan forgiveness
  • Flexible leave options
  • 403b retirement plan

Posting details

Employment type
Part Time
Work arrangement
On Site
Experience
2-5 yrs
Salary
$60,000 - $65,000/yr
Location
Colorado Springs, Colorado
Posted
Apr 30, 2026
Application
Employer website
TG

Hiring organization

The Geneva Foundation

The Geneva Foundation is a 501(c)3 nonprofit established in 1993 with the purpose to ensure optimal health for service members and the communities they serve. This purpose is accomplished through our mission to advance military medicine through research, development, and...

Salary listed on 10 jobs
IndustryResearch Services
TypeNonprofit
Size201-500 employees
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Market context

Colorado administration roles stay competitive

In Colorado, administration roles in clinical research often draw steady interest because employers look for candidates who can coordinate studies, manage documentation, and support compliance. This role is competitive because it asks for a bachelor’s degree, clinical research experience, and preferred skills in science-related study, electronic data capture systems, and project management. Review the AI-summarized requirements and benefits here to save time, then tailor your application to show direct research coordination experience.

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