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Exercise Training Research Coordinator Jobs (NOW HIRING)

Clinical Research Coordinator Salary: TBD Reports to: Arthroplasty Director The following ... Education/Training: Bachelor's degree required, Masters preferred Experience: 3+ years of ...

Research Coordinator

Roslyn, NY ยท On-site

$32 - $50/hr

Complete all required institutional, regulatory, and sponsor training. * Perform additional duties ... Ability to maintain confidentiality and exercise sound professional judgment. Posted Salary Range ...

Exercise appropriate discretion when handling sensitive patient and clinical information ... Skills training and professional development resources * Opportunity to gain experience supporting ...

Complete all required institutional, regulatory, and sponsor training. * Perform additional duties ... Ability to maintain confidentiality and exercise sound professional judgment. Posted Salary ...

Complete all required institutional, regulatory, and sponsor training. * Perform additional duties ... Ability to maintain confidentiality and exercise sound professional judgment. Pay RangeUSD $32.00 ...

Clinical Research Coordinator

Lake Worth, FL ยท On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) Location: Lake Worth, FL | Site Name: JEM Research Institute ... Maintain regulatory documentation and ensure proper training is completed for all study amendments ...

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Exercise Training Research Coordinator information

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How much do exercise training research coordinator jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for exercise training research coordinator in the United States is $28.15, according to ZipRecruiter salary data. Most workers in this role earn between $21.88 and $31.97 per hour, depending on experience, location, and employer.

What are popular job titles related to Exercise Training Research Coordinator jobs?

For Exercise Training Research Coordinator jobs, the most frequently searched job titles are:

Infographic showing various Exercise Training Research Coordinator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 17% Part Time, and 1% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $58,562 per year, or $28.2 per hour.

Research Coordinator

Huntsville, AL โ€ข On-site

$15 - $20/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago


Job description

Benefits:
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Research Coordinator – Clinical Trials
Rehabilitation & Neurological Services, LLC is seeking an experienced, organized, dependable, and motivated Clinical Research Coordinator to join our growing clinical research team. We are looking for a reliable professional who wants to grow with our organization long-term and become an integral part of a fast-paced, patient-centered research program.
This position requires someone who can work independently, prioritize responsibilities effectively, problem-solve proactively, and maintain professionalism while managing multiple clinical trials and deadlines.
Qualifications
* Minimum of 2–3 years of CLINICAL RESEARCH experience preferred
* Current GCP (Good Clinical Practice) training/certification required
* Medical office, nursing, allied health, or healthcare experience strongly preferred
* Prior experience coordinating pharmaceutical and/or device clinical trials
* Strong organizational, communication, and multitasking skills
* Ability to prioritize and manage multiple studies simultaneously
* Dependable, detail-oriented, and self-motivated
* Ability to work independently with minimal supervision
* Comfortable interacting with patients, sponsors, CROs, physicians, and monitors
* Proficiency with EMR systems, Microsoft Office, and electronic data entry systems
* Knowledge of IRB processes, informed consent, source documentation, adverse event reporting, and regulatory compliance
* Experience with recruitment, retention, and participant scheduling preferred
* Phlebotomy experience is a plus
* Bilingual candidates are encouraged to apply
Responsibilities
* Coordinate and manage day-to-day clinical trial activities
* Screen, recruit, and retain study participants
* Conduct and document informed consent procedures
* Schedule and coordinate study visits and follow-up appointments
* Ensure protocol compliance and participant safety
* Maintain accurate source documentation, regulatory binders, and study records
* Enter and resolve data queries in electronic data capture systems
* Communicate effectively with sponsors, CROs, monitors, investigators, and participants
* Prepare for sponsor monitoring visits, audits, and site initiation visits
* Assist with lab processing, specimen handling, shipping, and study-related procedures
* Track enrollment goals, study timelines, visit windows, and regulatory deadlines
* Participate in occasional weekend community engagement and outreach events related to research and education
* Support a positive, professional, team-oriented environment focused on excellence and growth
Application Requirements
Qualified applicants must submit:
* Current resume/CV
* List of clinical trials previously worked on
* Specific role/capacity on each study (Coordinator, Regulatory, Recruitment, Data Entry, etc.)
* Certifications and GCP training documentation
* Professional references
Preferred Therapeutic Experience
* Neurology
* Migraine/Headache Medicine
* Alzheimer’s Disease/Dementia
* Psychiatry
* Internal Medicine or Primary Care
We are seeking someone reliable, professional, organized, and committed to growing with a physician-led research program focused on innovation, patient care, and advancing clinical science. Competitive compensation will be based on experience and qualifications.