19,617 Clinical Research Associate Jobs (June 2026)
Clinical Research Associate jobs in June 2026 often center on site monitoring, trial documentation, protocol compliance, and communication with investigators, sponsors, and clinical operations teams. Listings may include on-site, remote, and hybrid CRA roles across early-stage studies, late-phase trials, and ongoing site management work. Create an account to explore the full job feed and auto-apply with LiftmyCV AI Agent.
Clinical Research Associate I/ Clinical Research Associate II
RemotePrecision for Medicine is seeking Clinical Research Associates I and II to enhance clinical trial execution in the life sciences sector. The role offers remote working flexibility, primarily targeting candidates based in the Paris area. Successful candidates will monitor and support clinical studies, while enjoying a positive work-life balance and a supportive company culture. Required qualifications include a life sciences degree and at least one year of CRA experience, particularly in oncology studies.
Posted 1 week ago
Senior Clinical Research Associate II
On-siteSyneos Health is seeking a Senior Clinical Research Associate II to join their clinical solutions team in Mumbai. This role involves extensive clinical monitoring experience, focusing on site selection, initiation, and activation. The ideal candidate will have a strong oncology background and will act as the primary point of contact for clinical sites. Responsibilities include ensuring compliance with regulations, assessing safety, documenting activities, and managing site-level communications. Join a dynamic team dedicated to driving progress in healthcare and delivering impactful solutions.
Posted 5 days ago
Senior Clinical Research Associate I
RemotePSI CRO seeks a Senior Clinical Research Associate I to join their dynamic and dedicated team. Founded in 1995, PSI is a global company specializing in clinical research for novel medications. The role involves communicating with project stakeholders, ensuring targets and timelines are met, and maintaining high quality standards. Ideal candidates will have a degree in Life Sciences, at least 3 years of monitoring experience, and be proficient in Japanese and English. PSI offers a supportive environment with growth opportunities in an innovative healthcare industry.
Posted 1 week ago
Clinical Research Associate II / Sr Clinical Research Associate
HybridAllucent is seeking a Clinical Research Associate (CRA II) or Senior Clinical Research Associate (Sr. CRA) to lead monitoring activities for investigational sites in France. In this role, you will ensure compliance with clinical trial protocols and regulations while mentoring junior team members. This position can be office-based in Paris or remote, providing opportunities to work collaboratively with a dedicated team to deliver results that matter. Join us to navigate the complexities of clinical trials and support the development of life-changing therapies.
Posted 1 week ago
Clinical Research Associate II
On-sitePSI CRO is a prominent Contract Research Organisation with over 30 years in the industry, emphasizing quality and timely clinical research services. As a Clinical Research Associate II, you'll oversee communication with project stakeholders and ensure compliance with clinical research standards. Key responsibilities include site management, monitoring visits, and maintaining data integrity. Required qualifications include a degree in Life Sciences, at least a year of monitoring experience, and proficiency in English, Spanish, and Catalan. PSI offers stability, a competitive salary, and opportunities for career development.
Posted today
Clinical Research Associate II
On-siteICON is seeking a Clinical Research Associate II (CRA II) to support clinical trials. This role focuses on designing and analyzing trials, ensuring compliance, and collaborating with investigators. Candidates should have at least 2 years of experience, a relevant Bachelor's degree, and strong communication skills. The position highlights the importance of integrity, collaboration, and inclusion as core values of ICON. Benefits include a competitive salary, health programs, and learning opportunities.
Posted 6 days ago
Clinical Research Associate II
On-siteJoin Fortrea as a Clinical Research Associate II and advance your clinical research career. You will play a crucial role in the successful delivery of clinical trials, supporting monitoring activities and ensuring compliance. This position suits individuals with at least one year of onsite experience looking to grow in a nurturing environment. You will gain exposure to various therapeutic areas while developing strong foundational skills in clinical research.
Posted 1 week ago
Clinical Research Associate II
On-siteAbbVie seeks a Clinical Research Associate II to support its R&D operations. This role involves ensuring the successful execution of clinical studies by monitoring investigative sites, ensuring compliance with regulations, and conducting site visits. Key responsibilities include training site personnel, managing investigator payments, and ensuring data quality and subject safety. Candidates should have a health-related tertiary qualification and at least a year of clinical experience, including on-site monitoring. Strong organizational skills and an understanding of clinical research regulations are essential.
Posted 2 weeks ago
Clinical Research Associate II
HybridAtriCure is seeking a Clinical Research Associate II (CRA II) to join their clinical affairs department. The CRA II will manage assigned clinical investigative sites, assisting with study protocol implementation and execution for clinical trials. Key responsibilities include site activity coordination, compliance monitoring, and training site personnel. Candidates should possess a science degree and two years of CRA experience, demonstrating knowledge of regulatory standards. This position provides opportunities for professional growth within a supportive and inclusive culture focused on innovative medical solutions for Afib treatment.
Posted 3 weeks ago
Clinical Research Associate II
On-siteJohnson & Johnson is seeking a Clinical Research Associate II (CRA II) to join their team fully remote across the U.S. The role involves coordinating clinical trials, ensuring compliance with protocols, and maintaining data quality. Candidates should hold a bachelor's degree in a scientific field with a minimum of 2 years in clinical research. Responsibilities include site visits, regulatory compliance, and teamwork to solve trial issues. The anticipated salary range for this position is $87,000 to $140,300, with additional benefits like retirement plans, generous vacation, and parental leave.
Posted 4 weeks ago
Senior Clinical Research Associate (CRA)
RemoteMapLight Therapeutics is seeking a Senior Clinical Research Associate specializing in clinical trials for central nervous system disorders. This remote position, requiring up to 75% travel, involves managing Investigator sites, conducting monitoring visits, and collaborating with internal and external stakeholders. The ideal candidate will have extensive experience in neuropsychiatry, including in-patient schizophrenia or Alzheimer's disease, and a solid understanding of Good Clinical Practices. Compensation ranges between $145,000 and $160,000 annually, along with a benefits package.
Posted 1 week ago
Clinical Research Associate I
On-siteSyneos Health is seeking a Clinical Research Associate I in Shanghai to join its Clinical Solutions team. The role involves site qualification, initiation, monitoring, and management, ensuring compliance with regulatory standards. Candidates should possess a bachelor's degree or RN, knowledge of Good Clinical Practice, and excellent interpersonal skills. The position requires managing travel of up to 75% and engaging in global clinical projects. This is an exciting opportunity to shape the future of healthcare within a collaborative and innovative team environment.
Posted 1 day ago
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Clinical Research Associate Salary Data (June 2026)
Review salary data for Clinical Research Associate jobs based on 19,617+ active postings, including CRA roles across clinical trial monitoring, site management, documentation, and compliance-focused research work.
Average Salary
$70k
$107k
$139k
25th
50th
75th
Based on 19,617 roles currently tracked by LiftmyCV. Last updated on Jun 23, 2026
Salary Distribution
Based on 19,617 roles currently tracked by LiftmyCV. Last updated on Jun 23, 2026
| Experience Level | 25th Percentile | Median (50th) | 75th Percentile | Sample Size |
|---|---|---|---|---|
| Overall | $70,050 | $106,784.25 | $138,975.63 | 9,310 |
| Entry-Level | $45,550 | $58,240 | $73,000 | 19 |
| Mid-Level | $81,250 | $106,784.25 | $124,125 | 42 |
| Senior-Level | $120,175 | $159,000 | $189,500 | 25 |
"Clinical Research Associate hiring in 2026 is less about broad clinical exposure and more about proof of trial execution. Employers tend to read for monitoring experience, site management, protocol compliance, documentation habits, and comfort with EDC or CTMS tools. For CRA roles, a resume that shows how you handled site issues, audit readiness, and cross-functional trial communication usually carries more weight than a general research background."
Marina's Market Take
Senior HR Leader & Lead Tech Recruiter
How to Land a Clinical Research Associate Role in 2026
Clinical research associate jobs usually reward candidates who can show disciplined trial monitoring, clean documentation habits, and comfort working across sites, sponsors, CROs, investigators, and study teams. In 2026, your application should make your trial exposure easy to understand: phases supported, therapeutic areas, monitoring model, site volume, protocol complexity, and whether you have worked in startup, maintenance, closeout, or a mix of study stages.
For CRA I and entry-level clinical research associate roles, position yourself around site coordination, regulatory document handling, source data review exposure, EDC familiarity, and GCP training. If your background is in clinical research coordination, study assistant work, nursing, pharmacy, or lab operations, connect that experience to patient visits, query resolution, informed consent support, IRB documentation, and investigator site communication.
For experienced CRA and senior CRA roles, lead with monitoring ownership. Be specific about site initiation visits, interim monitoring visits, closeout visits, protocol deviation follow-up, TMF quality, safety reporting workflows, and issue escalation. Employers reviewing clinical research associate applications want evidence that you can spot risk early, document findings clearly, and keep sites aligned with protocol, ICH-GCP, and sponsor expectations.
- Match your search to trial setting: separate CRO roles from sponsor-side CRA openings, academic medical center roles, and device or biotech studies.
- Use the right work-style filters: many CRA jobs differ sharply between regional travel, remote monitoring, hybrid site support, and on-site monitoring expectations.
- Spell out systems and documents: EDC, CTMS, eTMF, regulatory binders, monitoring visit reports, source documents, and query workflows all help place your experience.
- Target therapeutic fit: oncology, cardiology, neurology, infectious disease, rare disease, and medical device trials can each require different site habits and protocol fluency.
LiftmyCV helps you find clinical research associate jobs that match your skills, experience, and preferred work style, then auto-apply to relevant roles faster.
Required Skills
Resume Tips
A clinical research associate resume should show that you can monitor sites, protect protocol quality, and keep trial documentation inspection-ready. Prioritize experience with site initiation, interim monitoring, closeout visits, source data verification, query resolution, informed consent review, and adverse event documentation. If you’ve worked across Phase I to Phase IV studies, oncology, cardiology, rare disease, device trials, or decentralized trials, name those areas clearly.
Keep the resume practical. Cut broad claims like “excellent communicator” unless they’re tied to investigator meetings, site training, IRB submissions, or sponsor/CRO updates. Replace long task lists with proof of monitoring judgment, documentation accuracy, and follow-through. Tools and credentials matter here, so include systems such as Veeva Vault, Medidata Rave, Oracle Clinical, CTMS platforms, eTMF systems, EDC tools, and ICH-GCP training. Certifications such as ACRP-CRA or SOCRA CCRP can be worth placing near the top if current in 2026.
Weak bullet: Responsible for monitoring clinical trial sites and reviewing documents.
Stronger bullet: Conducted interim monitoring visits across multi-site Phase III studies, reviewed source data against EDC entries, resolved outstanding queries, and documented protocol deviations in CTMS and eTMF systems.
For entry-level CRA resumes, emphasize clinical trial assistant work, research coordinator experience, regulatory binder maintenance, patient visit tracking, lab kit coordination, and exposure to GCP procedures rather than unrelated healthcare duties.
LiftmyCV helps you create an ATS-friendly clinical research associate resume tailored to each job, so your skills and experience better match what employers are looking for.
How to Prepare for Interviews
Clinical Research Associate interviews usually center on monitoring judgment, protocol discipline, site communication, and documentation quality. Prepare examples from 2026 or earlier studies where you identified a source data discrepancy, handled a protocol deviation, followed up on missing regulatory documents, or escalated a patient safety concern without overstepping the CRA role.
Expect scenario questions rather than broad personality prompts. A common format is a monitoring visit case: you may be given incomplete source notes, delayed query responses, or temperature excursion records and asked how you would document findings, prioritize action items, and communicate with the site and study team. Practice walking through your reasoning in the order a CRA would actually work: protocol, ICH-GCP, source verification, site file review, issue escalation, and follow-up letter language.
Review your experience with EDC systems, CTMS updates, eTMF completeness, informed consent checks, adverse event reporting, and remote or on-site monitoring visits. Bring concise examples with study phase, therapeutic area, site count, and measurable cleanup results where possible.