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Junior Clinical Research Associate Jobs (NOW HIRING)

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Senior Clinical Research Associate

Chicago, IL · On-site +1

Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading ... as a mentor to junior staff, while maintaining site readiness for audits and inspections. * A ...

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Senior Clinical Research Associate

Blue Bell, PA · On-site +1

Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading ... as a mentor to junior staff, while maintaining site readiness for audits and inspections. * A ...

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

As of Jun 13, 2026, the average yearly pay for junior clinical research associate in the United States is $57,652.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,000.00 and $59,500.00 per year, depending on experience, location, and employer.

What is a Junior Clinical Research Associate job?

A Junior Clinical Research Associate (Jr. CRA) assists in monitoring clinical trials to ensure they comply with regulatory guidelines, protocols, and Good Clinical Practice (GCP). They support senior CRAs by reviewing study documents, conducting site visits, and ensuring data accuracy. Jr. CRAs also help in training site staff, managing trial documentation, and assisting with ethics submissions. This entry-level role serves as a stepping stone to becoming a full Clinical Research Associate (CRA). Strong organizational skills and attention to detail are essential for success in this position.

What are some typical challenges a Junior Clinical Research Associate might face in their first year on the job?

Junior Clinical Research Associates often face challenges such as managing multiple study sites, learning complex regulatory requirements, and adapting to the fast-paced nature of clinical trials. You'll need to balance on-site monitoring visits with timely documentation and communication between sponsors, sites, and internal teams. Many new associates also find adjusting to frequent travel and strict adherence to protocols demanding at first. With support from more experienced colleagues and continuous training, most individuals quickly develop confidence and master these essential aspects of the role. Overcoming these early challenges not only builds strong foundations for future advancement but also helps ensure the success of clinical research projects.

What are the key skills and qualifications needed to thrive in the Junior Clinical Research Associate position, and why are they important?

To excel as a Junior Clinical Research Associate, you need a bachelor’s degree in life sciences or a related field, a basic understanding of clinical trial methodology, and familiarity with Good Clinical Practice (GCP) guidelines. Proficiency in using clinical trial management systems (CTMS), electronic data capture (EDC), and an understanding of regulatory documentation are often required. Strong attention to detail, organization, and effective communication skills help build relationships with study sites and ensure accurate reporting. These competencies are crucial for maintaining study integrity, regulatory compliance, and smooth collaboration within research teams.

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Junior Clinical Research Associate jobs near you
Infographic showing various Junior Clinical Research Associate job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 66% Full Time, 27% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $57,652 per year, or $27.7 per hour.

Clinical Research Associate II (CRA II)

Biotronik

Lake Oswego, OR • On-site

Full-time

Posted 24 days ago

Job description

Clinical Research Associate II (CRA 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.
The Clinical Research Associate II (CRA II) supports the successful execution of clinical investigations by partnering closely with research sites, investigators, and internal clinical teams. This role is responsible for monitoring and supporting studies throughout all phases, including study start-up, enrollment, maintenance, and closeout activities.
The CRA II conducts on-site, remote, and centralized monitoring activities to ensure compliance with FDA regulations, ICH/GCP guidelines, study protocols, and company procedures. This position also serves as a key resource to research sites by providing training, guidance, and ongoing operational support. In addition, the CRA II may mentor junior clinical research staff and contribute to process improvement initiatives.
Your Responsibilities:
  • Conduct on-site, remote, and centralized monitoring visits in accordance with FDA regulations, ICH/GCP guidelines, study protocols, and company procedures.
  • Review study data for completeness, accuracy, and protocol compliance; identify discrepancies and support resolution of data queries and action items.
  • Prepare monitoring visit reports, follow-up letters, and related study documentation in a timely manner.
  • Support study start-up activities, including site qualification, regulatory document collection, IRB submissions, and site initiation activities.
  • Maintain study files and essential documentation, including regulatory records, training materials, correspondence, and investigational product accountability.
  • Ensure investigator and site documentation complies with applicable regulations and company standards.
  • Provide training and ongoing support to investigators, coordinators, field clinical staff, and internal study teams on protocol requirements and clinical research processes.
  • Build and maintain strong working relationships with investigators, coordinators, and research site personnel.
  • Identify compliance concerns, operational risks, and process gaps; collaborate with cross-functional teams to implement corrective actions and solutions.
  • Assist with the development and review of study-related materials, including case report forms, monitoring plans, training materials, and study tools.
  • Support investigational product/device accountability, inventory management, and documentation.
  • Contribute to clinical study operations, database development activities, investigator meetings, and continuous quality improvement initiatives.
  • Mentor and provide guidance to junior clinical research staff as needed.
  • Collaborate cross-functionally with internal departments to support clinical study objectives and timelines.
  • Perform additional duties and support other studies as assigned.

Your Profile
  • Bachelor's or advanced degree in Life Sciences, Nursing, or another health-related discipline required.
  • Minimum of 3 years of CRA experience within the medical device, pharmaceutical, or CRO industry required.
  • Strong working knowledge of FDA regulations, ICH/GCP guidelines, and clinical research processes.
  • Experience conducting monitoring visits and supporting clinical study execution.
  • Knowledge or experience in Electrophysiology and/or Neuromodulation preferred.
  • CCRA or CCRP certification preferred.
  • Strong organizational, time management, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Strong attention to detail and accuracy.
  • Proficiency with Microsoft Office applications and clinical database systems.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Valid U.S. driver's license required.
  • Ability to lift and transport up to 25 pounds.

Travel
  • Approximately 25% travel is required for site visits, monitoring activities, investigator meetings, training, and educational seminars.

Location
  • Remote opportunity based within the United States

Are you interested? Please apply online through our application management system! We are looking forward to welcoming you.
Location: Remote out of Lake Oswego, Oregon | Working hours: Full-time | Type of contract: Undefined
Apply now under: www.biotronik.com/careers
Job ID: 62284 | 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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