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Junior Cra Jobs (NOW HIRING)

Immatics NV

Senior Clinical Research Associate

$120K - $135K/yr

Mentor junior CRA team members and contribute to continuous improvement of clinical operations processes and procedures Travel required: Willingness to travel up to 75%. Valid Driver's License ...

Mindlance

Clinical Research Assocoate

San Diego, CA

The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical ... Provide guidance and training to junior level team members as assigned by management * Recommend ...

Thermo Fisher Scientific

CRA I/ II- FSP

Cornelius, NC · Remote

Work Schedule Environmental Conditions Ready to take the next step in your CRA career? At CRG ... We are hiring both Junior and experienced CRAs who are passionate about clinical research and eager ...

Thermo Fisher Scientific

CRA I/ II- FSP

Cornelius, NC · Remote

Work Schedule Environmental Conditions Ready to take the next step in your CRA career? At CRG ... We are hiring both Junior and experienced CRAs who are passionate about clinical research and eager ...

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Junior Cra information

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$19K

$52.5K

$88K

How much do junior cra jobs pay per year?

As of Jun 9, 2026, the average yearly pay for junior cra in the United States is $52,462.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,000.00 and $57,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a Junior Clinical Research Associate (CRA) during site monitoring visits?

As a Junior CRA, one common challenge during site monitoring visits is balancing thorough oversight with building positive relationships with site staff. You may encounter incomplete documentation, protocol deviations, or data discrepancies that require careful attention and clear communication. Additionally, learning to prioritize tasks efficiently and adapt to varying site procedures is essential. Over time, you'll develop confidence in addressing issues, ensuring regulatory compliance, and supporting sites effectively.

What is the difference between Junior Cra vs Clinical Research Associate?

AspectJunior CraClinical Research Associate
Required CredentialsTypically a bachelor's degree in life sciences or related field; some roles may require certificationSame as Junior Cra, often with additional certifications preferred
Work EnvironmentEntry-level, often in clinical trial sites or research teamsMore experienced, overseeing multiple sites or studies
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Common Search & ComparisonYesYes

The main difference between a Junior Cra and a Clinical Research Associate is experience level. Junior Cras are entry-level roles focusing on supporting clinical trials, while Clinical Research Associates are more experienced professionals responsible for monitoring and managing clinical studies. Both roles require similar educational backgrounds and are used in the same industry settings.

Is it hard to get a CRA job?

Securing a Junior CRA (Clinical Research Associate) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with some experience or training in clinical trials. Strong organizational skills, attention to detail, and familiarity with regulatory requirements and monitoring tools improve job prospects, but entry-level roles may still have a competitive application process.

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

To thrive as a Junior CRA, you need a background in life sciences or a related field, attention to detail, and a solid understanding of clinical trial protocols and regulatory requirements. Familiarity with electronic data capture (EDC) systems, Microsoft Office Suite, and GCP (Good Clinical Practice) certification is typically required. Strong organizational skills, communication, and an ability to manage time effectively are standout soft skills for this role. These competencies are crucial for ensuring the accuracy, compliance, and smooth execution of clinical studies.

What are Junior CRAs?

Junior Clinical Research Associates (Junior CRAs) are entry-level professionals who assist in the monitoring and management of clinical trials. They work under the supervision of more experienced CRAs to ensure that clinical research studies comply with regulatory requirements and study protocols. Their responsibilities often include site visits, reviewing documentation, ensuring data quality, and supporting communication between study sites and sponsors. Junior CRAs gain valuable experience that can lead to more senior roles in clinical research.
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Junior Cra jobs near you

Clinical Research Associate II (CRA II)

Biotronik

Lake Oswego, OR • On-site

Full-time

Posted 20 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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