23,093 Clinical Research Associate Jobs (July 2026)
Clinical Research Associate jobs in July 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 II - Senior Clinical Research Associate I
RemoteSyneos Health is a leading life sciences services organization focused on drug development and commercialization. The role of Clinical Research Associate II involves site management activities including qualification, monitoring, and close-out visits, ensuring compliance with guidelines. Candidates will be engaged in a collaborative environment and will play a significant role in advancing healthcare by fostering diverse teamwork and innovative problem-solving. Qualifications include a Bachelor’s degree in a related field, knowledge of regulatory requirements, and strong communication skills.
Posted 2 weeks 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 3 weeks ago
Clinical Research Associate / Senior Clinical Research Associate
HybridJoin PSI CRO, a dynamic mid-size global company with over 3,000 dedicated individuals, as a Clinical Research Associate / Senior Clinical Research Associate. This hybrid role involves conducting onsite and remote monitoring visits, training less experienced colleagues, and managing site communications in Germany and Switzerland. You will enjoy a supportive environment that fosters ownership and collaboration, with opportunities for career progression in a technologically integrated setting that values quality and patient safety.
Posted today
Senior Clinical Research Associate I
On-siteSyneos Health is a leading organization in life sciences services focused on accelerating customer success across drug development and commercialization. The role of Senior Clinical Research Associate I in Beijing involves monitoring clinical research studies, ensuring compliance, and collaborating with teams to support clinical trial operations. Candidates should possess a relevant bachelor's degree, a minimum of 2-4 years of clinical monitoring experience, and excellent communication skills. The company emphasizes career development and an inclusive culture, striving to create impactful healthcare solutions.
Posted 1 week 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 4 weeks ago
Senior Site Start up Associate / Senior Clinical Research Associate
HybridPremier Research seeks a Senior Site Start up Associate/Senior Clinical Research Associate (hybrid) to join their Regulatory Submissions and Contracts team. This role involves assisting biotech, medtech, and specialty pharma companies in transforming ideas and science into new medicines and technology, thus positively impacting lives. The job emphasizes growth, flexibility, and the value of team member input. Responsibilities include managing regulatory submissions and contracts while ensuring compliance with local and international regulations. Candidates should have relevant degrees and 3-5 years of experience in clinical trial submissions.
Posted 2 weeks 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 4 weeks ago
Clinical Research Associate II
On-siteAbbVie is seeking a Clinical Research Associate II to manage clinical operations and ensure protocol compliance at investigative sites. This role involves monitoring activities, conducting site visits, and ensuring data quality and safety of study subjects. Applicants should have at least one year of clinical experience and possess advanced skills in planning, collaboration, and leveraging technology. The ideal candidate will contribute to innovative solutions in clinical research while adhering to regulatory guidelines and promoting a culture of integrity and excellence.
Posted 1 day ago
Clinical Research Associate II
On-siteJoin Parexel as a Clinical Research Associate II, where you'll play a pivotal role in improving global health through clinical trials and regulatory solutions. You will be responsible for monitoring study performance, supporting investigators and site staff, and ensuring compliance with local regulations. Required skills include strong knowledge of clinical study processes, good computer skills, and fluency in English. Ideal candidates have at least two years of experience and a bachelor's degree in a biological science or healthcare-related field.
Posted 6 days ago
Clinical Research Associate II
RemotePrecision for Medicine is a unique CRO focused on improving clinical trials for life sciences. With an emphasis on Oncology and Rare Disease, the company combines cutting-edge technology and expertise to enhance the efficiency of bringing therapies to patients. They pride themselves on high CRA retention rates and provide a supportive work environment. This position requires monitoring clinical studies, helping with regulatory submissions, and ensuring compliance. Ideal candidates are detail-oriented, possess strong communication skills, and have a commitment to quality.
Posted 1 week ago
Clinical Research Associate II
On-siteFortrea is seeking a Clinical Research Associate II to manage site responsibilities for clinical trials. This role involves conducting monitoring visits, ensuring compliance with protocols and regulations, and verifying data integrity. The successful candidate will work independently and collaboratively to ensure quality and efficiency in monitoring clinical studies. A strong understanding of GCP guidelines and prior clinical monitoring experience are required, along with excellent communication and problem-solving skills.
Posted 2 weeks ago
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 3 weeks ago
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Clinical Research Associate Salary Data (July 2026)
Review salary data for Clinical Research Associate jobs based on 23,093+ 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 23,093 roles currently tracked by LiftmyCV. Last updated on Jun 23, 2026
Salary Distribution
Based on 23,093 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.