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Junior Clinical Research Associate Jobs (NOW HIRING)

Medasource

$96 - $103/hr

Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region ... junior team members. This is an excellent opportunity for an experienced clinical research ...

Manhattan Research

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Senior Clinical Research Coordinator

New York, NY · On-site

$80K/yr

... junior staff, and serve as a primary point of contact for sponsors, CRAs, and the Principal ... to junior clinical research coordinators. · Identify and troubleshoot study-level issues ...

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Urgent

UAB

CLINICAL RESEARCH ADMINISTRATOR III

Tampa, FL · On-site

$55K - $89K/yr

The position is responsible for administrative and financial oversight of departmental-sponsored research, as well as OnCore report analysis and junior clinical research staff training. General ...

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

As of Sep 5, 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?

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 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $57,652 per year, or $27.7 per hour.

Sr. Clinical Research Associate (NE)

Medasource

On-site

$96 - $103/hr

Other

Posted 4 days ago

Job description

Sr. Field Clinical Research Associate
Remote with Travel required in the North Central Region (ideally based out of Boston, MA or Philadelphia, PA)
Hybrid role
Compensation: $70 – $75 per hour

ABOUT THE ROLE

Our client, a leading life sciences company, is seeking a Sr. Field Clinical Research Associate for a remote, travel-based, part-time 12-month contract position focused on the North Central Region, with the possibility of extension. In this hybrid role, you will be responsible for monitoring clinical studies at assigned sites to ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols. You will play a key role in site initiation, periodic and close-out visits, data and documentation review, adverse event and protocol deviation reporting, and resolution of site issues. The position involves close coordination with study teams, enrolling sites and subjects, facilitating data query resolution, and mentoring junior team members. This is an excellent opportunity for an experienced clinical research professional with a strong background in cardiac, vascular, or neuromodulation technologies.

WHAT YOU’LL DO
  • Monitor clinical studies at sites in your assigned territory (and others as requested) to ensure compliance with regulatory requirements, Good Clinical Practice, and study protocols, including site initiation, periodic, and close-out visits.
  • Ensure both regulatory and clinical protocol compliance is maintained for all assigned clinical projects.
  • Review data and source documentation from investigational sites for accuracy and completeness.
  • Ensure timely and accurate reporting of adverse events, protocol deviations, device complaints, and malfunctions according to company policies and procedures.
  • Resolve and/or facilitate resolution of site issues, including identification of root causes and actions to prevent recurrence.
  • Coordinate with study teams, field clinical engineers, and specialists to enroll sites into new and ongoing clinical studies.
  • Facilitate enrollment of study subjects via site coordinators and support resolution of data queries and action items at clinical sites.
  • Promptly report findings of monitoring visits according to established processes.
  • Collaborate with in-house teams to ensure complete and timely submission of study documents.
  • Participate in conference calls and training sessions as required.
  • Train site personnel to ensure compliance with study protocols and local regulations.
  • Mentor less experienced clinical team members as requested.
  • Demonstrate a high level of written and verbal communication skills with internal and external customers.
WHAT YOU BRING
  • Bachelor’s degree from an accredited university or college, preferably in natural science, pre-medicine, nursing, bioengineering, or a related field.
  • Minimum five years of clinical research experience with a superb understanding of all aspects of clinical research.
  • Strong written, verbal, interpersonal, presentation, analytical, and organizational skills.
  • Ability to interpret basic clinical data, meet deadlines, and communicate effectively with all levels of employees.
  • Proficiency with word processing software and relevant clinical applications.
  • Ability to work independently and within a dynamic, global team environment.
  • Ability to exchange straightforward information, ask questions, and check for understanding.
  • Familiarity with cardiac, vascular, and/or neuromodulation technologies.
  • Prior clinical monitoring experience (strongly preferred).
  • Experience in a medical device/pharmaceutical company or clinical/hospital environment (preferred).
  • Certification by an industry-recognized professional society (e.g., SoCRA, ACRP) or accredited institution (preferred).
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