9,019 Clinical Research Associate Jobs (November 2026)
Clinical Research Associate jobs in November 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
RemotePrecision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the…
Posted 1 week ago
Clinical Research Associate II/ Senior Clinical Research Associate
RemotePrecision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the…
Posted 1 week ago
Clinical Research Associate II/ Senior Clinical Research Associate
HybridJoin PSI CRO as a Clinical Research Associate II/Senior Clinical Research Associate, where you'll ensure the quality and integrity of clinical trials. Act as the key communication point between clinical trial sites and project teams, building strong…
Posted 3 weeks ago
Senior Clinical Research Associate I/II
RemoteSyneos Health is seeking a Senior Clinical Research Associate I/II to oversee site management and ensure compliance throughout the clinical trial process. This role involves coordinating site qualifications, monitoring, and addressing site…
Posted 2 weeks ago
Senior Clinical Research Associate I
RemoteJOB SUMMARY The Senior Clinical Research Associate I is responsible for the site management, site monitoring and close out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with…
Posted 3 weeks ago
Clinical Research Associate II
HybridJob Description We are seeking a highly motivated Clinical Research Associate II (CRA II) to join our Clinical Development team. In this role, you will be accountable for the performance and compliance of assigned protocols and sites within the…
Posted today
Clinical Research Associate II
On-siteJoin PSI CRO as a Clinical Research Associate II, where you'll manage the clinical aspects of global projects. Based in Bangkok, Thailand, you'll engage directly with project stakeholders, conduct monitoring visits, and ensure compliance with clinical…
Posted today
Clinical Research Associate II
On-siteAtriCure is seeking a Clinical Research Associate II (CRA II) to support its clinical affairs department. The CRA II will manage assigned clinical investigative sites, implement study protocols, and ensure compliance with Good Clinical Practice (GCP)…
Posted 1 day ago
Clinical Research Associate II
On-siteAbbVie is seeking a Clinical Research Associate II to drive the execution of clinical trials across various therapeutic areas, ensuring compliance with regulations and quality standards. The role involves mentoring junior staff, conducting monitoring…
Posted 1 day ago
Clinical Research Associate II
On-siteJoin Worldwide Clinical Trials as a Clinical Research Associate II and make a significant impact in the field of clinical research. This home-based role involves managing clinical studies with a focus on quality, patient safety, and regulatory compliance.…
Posted 1 day ago
Clinical Research Associate II
On-siteJoin Parexel as a Clinical Research Associate II, where you will work closely with clinical sites to ensure adherence to study protocols and quality data collection. Responsibilities include building relationships with investigators, performing on-site…
Posted 5 days ago
Clinical Research Associate II
On-siteAs a Clinical Research Associate II at ICON Strategic Solutions, you will play a pivotal role in designing and analyzing clinical trials, ensuring protocol compliance, and contributing to innovative treatments. With over 90 sponsor partnerships, ICON…
Posted 6 days ago
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Clinical Research Associate Salary Data (November 2026)
Review salary data for Clinical Research Associate jobs based on 9,019+ active postings, including CRA roles across clinical trial monitoring, site management, documentation, and compliance-focused research work.
Average Salary
$63k
$87k
$132k
25th
50th
75th
Based on 9,019 roles currently tracked by LiftmyCV. Last updated on Oct 22, 2026
Salary Distribution
Based on 9,019 roles currently tracked by LiftmyCV. Last updated on Oct 22, 2026
| Experience Level | 25th Percentile | Median (50th) | 75th Percentile | Sample Size |
|---|---|---|---|---|
| Overall | $62,962.38 | $86,760 | $131,557.13 | 9,019 |
| Entry-Level | $47,601.38 | $61,502.25 | $83,625 | 38 |
| Mid-Level | $65,564.63 | $76,096 | $105,250 | 64 |
| Senior-Level | $133,706.25 | $176,207.75 | $203,300 | 34 |
"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.