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Regional Clinical Research Associate Jobs (NOW HIRING)

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... SCRA II (5+ yrs) - oversees complex sites/regions, mentors peers, and drives process improvements

Icon plc

Senior Clinical Research Associate

Houston, TX · Hybrid

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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Regional Clinical Research Associate information

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$11K

$79.4K

$137.5K

How much do regional clinical research associate jobs pay per year?

As of Jul 17, 2026, the average yearly pay for regional clinical research associate in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are some common challenges Regional Clinical Research Associates face when managing multiple study sites?

Regional Clinical Research Associates (CRAs) often juggle overseeing several clinical trial sites, which can present challenges such as coordinating travel schedules, maintaining consistent communication with site staff, and ensuring all sites comply with study protocols and regulatory requirements. Balancing administrative duties with on-site monitoring visits requires strong organizational and time-management skills. Additionally, adapting to varying site cultures and addressing site-specific issues are essential for maintaining study quality and fostering effective collaboration.

What are the key skills and qualifications needed to thrive as a Regional Clinical Research Associate, and why are they important?

To thrive as a Regional Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory requirements, and a relevant life sciences degree, often complemented by industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Strong organizational, problem-solving, and communication skills help manage multiple sites, build rapport with investigators, and ensure protocol compliance. These competencies are critical for maintaining data integrity, ensuring regulatory compliance, and supporting successful clinical trial outcomes across diverse locations.

What is a Regional Clinical Research Associate?

A Regional Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials at sites within a specific geographic region. They ensure that clinical studies are conducted according to protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Regional CRAs act as a liaison between the clinical trial sponsor and research sites, performing site visits, verifying data accuracy, and ensuring patient safety. Their work helps ensure the integrity and reliability of clinical trial data while supporting the successful completion of research studies.

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

AspectRegional Clinical Research AssociateClinical Research Associate
Required CredentialsBachelor's degree, clinical research certification often preferredBachelor's degree, clinical research certification often preferred
Work EnvironmentTravel across multiple sites within a regionMonitor specific sites, often within a local area
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentUnderstanding regional responsibilities and scopeMonitoring specific clinical trial sites

The main difference between a Regional Clinical Research Associate and a Clinical Research Associate lies in their scope of work. The Regional CRA oversees multiple sites within a region, often traveling extensively, while the CRA typically monitors individual sites within a specific area. Both roles require similar credentials and are employed in the same industry sectors, but their geographic focus and daily responsibilities differ.

What Does a Regional Clinical Research Associate Do?

A regional clinical research associate works to manage studies and clinical trials associated with pharmaceutical and biotechnological drugs, products, and procedures. Your responsibilities in this career include writing and creating trial protocols, assisting in the scientific research that determines the efficacy and safety of vaccines or a medication, liaising with the ethics committee about trial subject safety, rights, and well-being, and training staff on protocol, case report form completion, and proper source documentation. Other duties include conducting research analysis, documenting and overseeing IP inventory, liaising with regulatory authorities, and tracking, managing, and ordering trial and IP materials.

More about Regional Clinical Research Associate jobs
Who are the top companies hiring for Regional Clinical Research Associate jobs? The top employers for Regional Clinical Research Associate jobs are:
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Regional Clinical Research Associate jobs near you
Infographic showing various Regional Clinical Research Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Regional Clinical Research Associate II

Biotronik

Lake Oswego, OR • On-site

Full-time

Posted 19 days ago

Job description

Regional Clinical Research Associate II
BIOTRONIK is one of the leading manufacturers of cardio- and endovascular implants and catheters for cardiac rhythm management, electrophysiology and vascular intervention. As a globally active company headquartered in Berlin, Germany, we develop, produce and distribute high-quality medical products based on the latest technology and research. Our success is based on the competence and results-oriented cooperation of our employees.
BIOTRONIK is looking to add a Regional Clinical Research Associate II to our Clinical Studies team. Conduct on-site, remote, and centralized monitoring to ensure compliance with FDA regulations, ICH/GCP guidelines, BIOTRONIK procedures, and IRB/EC policies. Supports clinical studies in cardiac rhythm management and related areas by ensuring data integrity, subject safety, and protocol adherence.
Your Responsibilities:
  • Conduct monitoring activities in accordance with BIOTRONIK procedures and applicable regulations to evaluate protocol compliance, data accuracy, and subject safety through review of regulatory documents, medical records, reported data, and investigational device accountability (as applicable).
  • Manage all monitoring responsibilities for assigned clinical studies, including:
    • Scheduling and completing monitoring visits within established timelines in alignment with risk-based monitoring plans and internal procedures.
    • Identifying data discrepancies and compliance issues; communicating findings to site staff, providing retraining where necessary, and developing effective resolution strategies.
    • Escalating significant issues to the study team and department management through appropriate channels, including monitoring visit reports.
  • Collaborate closely with Investigators and Research Coordinators during monitoring visits to ensure compliance, address findings, and support timely issue resolution.
  • Partner with BIOTRONIK Clinical Studies team members to prepare for site visits, proactively assess site performance, and escalate critical findings.
  • Present monitoring outcomes to site staff with clear guidance on corrective actions; review and resolve data queries to ensure mutual understanding and closure.
  • Serve as an ongoing resource to study sites between visits, providing guidance on data queries, action items, and study requirements.
  • Train and mentor BIOTRONIK staff on monitoring processes and best practices; conduct site training and co-monitoring visits as requested.
  • Complete all required documentation, including monitoring reports, follow-up letters, and action items, in accordance with BIOTRONIK standards.
  • Support departmental and study-related initiatives, including audits, investigator meetings, and training activities, in collaboration with the Manager, CRA Group.
  • Interface effectively with cross-functional teams, including Clinical, Regulatory, Sales, and site personnel, to support study execution.

Your Profile
  • Bachelor's degree or higher level degree in nursing, life sciences or related medical/scientific field.
  • Must have a valid US driver's license.
  • Minimum of 3 years on-site monitoring research experience for a CRO, Pharma, or Medical Device company. Experience supporting medical device IDE trials is preferred.
  • Strong clinical trial monitoring experience in relevant BIOTRONIK product and/or relevant therapeutic areas (electrophysiology and vascular interventional cardiology) preferred.
  • Demonstrated experience in clinical trial monitoring, preferably within electrophysiology, cardiology, or related therapeutic areas.
  • Experience monitoring first-in-human (FIH), investigational device exemption (IDE), post-approval, and/or post-market studies.
  • Strong understanding of GCP/ICH guidelines and FDA regulations, including 21 CFR Parts 11, 50, 54, 56, 812, and 820, as well as ISO standards for medical device clinical trials.
  • Current certification as a Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP).
    Solid knowledge of medical terminology.
  • Ability to work independently with minimal supervision in a regional territory.
  • Strong organizational, analytical, and problem-solving skills, with the ability to assess complex situations and develop effective solutions.
  • Excellent interpersonal and communication skills, with the ability to engage effectively with physicians, site staff, cross-functional teams, and leadership.
  • Ability to communicate protocol and regulatory requirements clearly and constructively.
  • Responsible for adequate and reasonable home office set up including dedicated desk space to accommodate work responsibilities and BIOTRONIK supplied equipment.

Travel
  • Approximately 75% travel required throughout the United States to investigational centers and BIOTRONIK, Inc. corporate office. Travel frequency may vary based on study needs and may include air, ground, or rail travel.

Location
  • Remote opportunity based in the Midwest, Southwest or Southeast

Are you interested? Please apply online through our application management system! We are looking forward to welcoming you.
Location: Midwest, southwest or Southeast, United States | Working hours: Full-time | Type of contract: Undefined
Apply now under: www.biotronik.com/careers
Job ID: 62419 | BIOTRONIK Inc. | United States (US)
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law. Please note that applications sent by post will only be returned if a sufficiently stamped self-addressed envelope is included.

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