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Regional Study Coordinator Jobs (NOW HIRING)

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of ... Benefits may vary by role, country, region, union status, and other employment status factors. You ...

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of ... Benefits may vary by role, country, region, union status, and other employment status factors. You ...

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities ... Maintains familiarity with all protocols being conducted at sites within the assigned region and ...

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities ... Maintains familiarity with all protocols being conducted at sites within the assigned region and ...

MO · On-site

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities ... Maintains familiarity with all protocols being conducted at sites within the assigned region and ...

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities ... Maintains familiarity with all protocols being conducted at sites within the assigned region and ...

COC CE Coordinator

Atlanta, GA · On-site

$50K - $57K/yr

... region of the Balance of State (BoS) CoC. This work is done alongside three CE System Coordinators and reports to the Coordinated Entry Team Lead. The CE Coordinator will ensure that all HUD required ...

The successful applicant will serve as a liaison with national and regional study coordinating centers and with other participating treatment sites. -Partner with aligned senior leaders to determine ...

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Regional Study Coordinator information

See salary details

$33.5K

$67.8K

$115.5K

How much do regional study coordinator jobs pay per year?

As of Jul 28, 2026, the average yearly pay for regional study coordinator in the United States is $67,779.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $79,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Regional Study Coordinators, and how can they be effectively managed?

Regional Study Coordinators often encounter challenges such as coordinating across multiple sites, managing diverse teams, and ensuring consistent study protocols despite regional differences. Effective communication and strong organizational skills are key to overcoming these hurdles. Leveraging regular meetings, clear documentation, and collaboration tools can help maintain alignment among all stakeholders, while proactive problem-solving ensures that any site-specific issues are addressed quickly and efficiently.

What is the difference between Regional Study Coordinator vs Clinical Research Associate?

AspectRegional Study CoordinatorClinical Research Associate
CredentialsBachelor’s degree in health sciences or related field; often requires certification in clinical researchBachelor’s degree in life sciences or health sciences; often requires certification in clinical research
Work EnvironmentCoordinates multi-site clinical studies, liaising with sites and sponsorsMonitors clinical trial sites, ensuring compliance and data integrity
Employer & IndustryPharmaceutical companies, CROs, academic institutionsPharmaceutical companies, CROs, biotech firms

The Regional Study Coordinator and Clinical Research Associate roles share similar educational backgrounds and work within the clinical research industry. While the Coordinator manages study operations across multiple sites, the Associate primarily monitors individual trial sites. Both roles are essential for successful clinical trials and often collaborate closely.

What does a Regional Study Coordinator do?

A Regional Study Coordinator manages and oversees clinical research studies within a specific geographic area or set of sites. Their responsibilities include coordinating study activities, ensuring regulatory compliance, supervising site staff, monitoring data collection, and serving as a liaison between study sponsors and local research teams. They play a crucial role in making sure studies are conducted efficiently, ethically, and according to protocol, while also resolving issues that arise during the study process.

What are the key skills and qualifications needed to thrive as a Regional Study Coordinator, and why are they important?

To thrive as a Regional Study Coordinator, you need strong project management abilities, knowledge of clinical research protocols, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and sometimes certifications like SOCRA or ACRP are advantageous. Excellent organization, communication, and problem-solving skills help you coordinate effectively across multiple sites and stakeholders. These competencies are crucial to ensure studies are executed smoothly, compliantly, and on schedule across diverse regions.
More about Regional Study Coordinator jobs
What cities are hiring for Regional Study Coordinator jobs? Cities with the most Regional Study Coordinator job openings:
What states have the most Regional Study Coordinator jobs? States with the most job openings for Regional Study Coordinator jobs include:
Infographic showing various Regional Study Coordinator job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $67,779 per year, or $32.6 per hour.
Study Coordinator

Study Coordinator

Portland VA Research Foundation

Portland, OR • On-site

$32.19/hr

Full-time

Posted 17 days ago


Job description

Job Title: Study Coordinator

Department: Research

Reports To: John Mastronarde

FLSA Status: Full Time, Non-exempt

Pay Rate: $32.19 per hour

Work Type: Onsite

POSITION SUMMARY

The Study Coordinator will assist in the coordination and execution of multiple elements in human subjects research within the VA Portland Health Care System (VAPORHCS), with primary emphasis on assisting the lead study coordinator and local Primary Investigator of the project: Development and Evaluation of a Care Pathway for Evaluation and Management of the Respiratory Syndromes of Amyotrophic Lateral Sclerosis (ALS) [CAPRESA]. The lead study coordinator is based at the central site for this study, Rocky Mountain Regional VA Medical Center in Aurora, CO. Flexibility, time management, customer service, and a team-based aptitude are key.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Identify, communicate with, recruit, and enroll Veterans to participate in the study
  • Conduct informed consent and administer surveys to patients
  • Maintain a working knowledge of FDA and IRB guidelines that govern research
  • Enter patient data into electronic database systems
  • Clean, package, and ship diagnostic testing equipment to patients and be prepared to provide technical support for common issues using the equipment
  • Modify or develop study training materials for equipment use
  • Download data stored on testing devices returned by patients
  • Assist qualitative research staff with qualitative data collection as needed, including reading prepared questions to patients and recording their verbal responses using automated transcription software
  • Maintain organized and accurate study records
  • Support coverage across the study team, stepping in when necessary to screen and enroll patients, request and review medical records, assist Principal Investigator with document preparation, including regulatory materials such as IRB forms, or manuscript writing, and other study related tasks, as needed
  • Attend research coordinator educational opportunities at OHSU and the Portland VA
  • Other duties as assigned by Principal Investigator and manager

SUPERVISORY RESPONSIBILITY

This position has no direct reports.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and EXPERIENCE

  • Bachelor's degree or higher; preferably in a scientific or social science discipline
  • Previous experience with human subjects' research
  • Previous experience with veteran population preferred

KNOWLEDGE, SKILLS, AND ABILITIES

  • Ability to work in a fast-paced environment and meet critical deadlines
  • Ability to clearly organize and/or adapt to multiple priorities at one time
  • Ability to work well with other people as well as independently
  • Strong communication skills, with the ability to communicate clearly in English with Veterans of all backgrounds
  • Critical thinking skills to interpret, implement, and facilitate clinical research protocols
  • Proficiency with Microsoft Office applications
  • Able to use critical thinking skills to make decisions that are within scope, and to recognize when decisions are out of scope.

ADDITIONAL INFORMATION

Because this position is based in a VA facility, the Research Assistant must secure a VA Without Compensation Appointment (WOC) prior to starting work, and must maintain a WOC Appointment in order to continue employment.

The VA's WOC process will be facilitated by the supervisor and processed through the VA Research and Development office. The screening process required to obtain a WOC may include a background check, a credit check, a physical, a drug test, and a TB test.

After the WOC process has been completed, the VA also requires several trainings prior to employees starting work.

Portland VA Research Foundation is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, color, sex, sexual orientation, gender identity, religion, national origin or age.

All PVARF employees are required to be fully vaccinated for COVID-19 within 8 weeks of hire, unless medically exempt. Employees will be required to provide either proof of vaccination or an approved medical exemption prior to beginning work.


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