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Junior Clinical Research Associate Jobs (NOW HIRING)

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Icon plc

Senior Clinical Research Associate

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...

BeiGene, Inc.

Senior Clinical Research Associate

$105K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Research Associate (SCRA) is primarily a site monitor and is responsible for ... junior clinical staff. Supervisory Responsibilities: • Provides site level management for ...

BeiGene USA

Senior Clinical Research Associate

$105K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Research Associate (SCRA) is primarily a site monitor and is responsible for ... to junior clinical staff. Supervisory Responsibilities: Provides site level management for ...

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

As of Aug 16, 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.

Is it hard to get a junior clinical research associate job?

Securing a junior clinical research associate position can be competitive, often requiring a relevant bachelor's degree in life sciences or related fields, along with strong organizational and communication skills. Entry-level roles may also prefer candidates with some internship or research experience and familiarity with clinical trial protocols and regulatory requirements.

What is a junior clinical research associate?

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 August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $57,652 per year, or $27.7 per hour.

Senior Clinical Research Associate - CNS

Cognitive Research Corporation

Remote

Full-time

Re-posted 9 days ago

Job description

The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Essential Duties & Responsibilities
  • Initiates, monitors, and closes-out investigative sites in accordance with FDA/ICH regulations.
  • Tracks and maintains study specific non-Case Report Form database
  • Administers Clinical research projects; collects investigator documentation, site management, clinical contact, and prepare reports as required
  • Ensures appropriate source document review and source document verification as required
  • Reviews Case Report Forms to identify erroneous, missing, or incomplete data
  • Generates queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly
  • Verifies study drug accountability; generates and tracks drug shipments and storage
  • Travels as necessary, based on project needs and according to Clinical Monitoring Plan requirements
  • Performs data collection, retrieval, entry and clean up as necessary
  • Develops and maintains strong relationships with Investigator(s) and site staff
  • Independently manages sites resulting in acceptable Quality Assurance reports.
  • Escalates study/site issues/deviations appropriately
  • Serves as lead monitor for a protocol or project by creating study files, arranges monitoring schedules, leads the project team, organize and run meetings and performs other project management duties as assigned by management
  • Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format
  • Reports, writes narratives, and follows-up on reported serious adverse events
  • Interacts and attends client meetings, as appropriate
  • Mentors junior staff/CRAs
  • Quality oversight checks of monitoring
  • Performs other duties as assigned

Qualifications
  • Bachelor's degree, or RN, in a related field or equivalent combination of education, training and experience
  • Minimum 5 years' experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
  • Ability to work and travel independently with minimal supervision
  • Experience with numerous EDC systems.
  • Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Office, Zoom and Adobe
  • Excellent writing and verbal skills, English language proficiency
  • Meticulous attention to detail
  • Time management and ability to prioritize tasks
  • Ability to travel up to 70%

Department Clinical Operations Role Senior Clinical Research Associate Locations Remote, US Remote status Fully Remote Employment type Full-time

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