3,624 Remote Clinical Research Jobs (June 2026)
Remote clinical research jobs in June 2026 can include work across clinical trial coordination, study operations, data review, regulatory documentation, site support, and patient-facing research administration. Listings may range from entry-level clinical research assistant roles to experienced clinical research associate, trial manager, and study start-up positions, with remote requirements varying by employer and protocol. Create an account to explore the full job feed and auto-apply with LiftmyCV AI Agent.
Senior Clinical Trial Coordinator
RemoteThe Senior Clinical Trial Coordinator (Sr. CTC) role involves comprehensive trial and site administration, document management, and regulatory compliance. Key responsibilities include managing clinical supply, coordinating site start-up activities, ensuring timely submissions to authorities, and collaborating with finance for budgeting and payments. The position serves as a Subject Matter Expert (SME) to improve processes and mentor junior staff. Candidates should have at least 3 years of clinical research experience and strong communication and organizational skills.
Posted 6 days ago
Freelance Regional Clinical Trial Coordinator
RemoteRho is seeking a Freelance Regional Clinical Trial Coordinator for a full-time, home-based position. The coordinator will play a crucial role in preparing Investigator Site Files, maintaining Trial Master Files, and ensuring effective communication between stakeholders. Join a dynamic team dedicated to redefining clinical research and healthcare.
Posted 3 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
Senior Clinical Research Associate
RemoteJoin Danaher as a Senior Clinical Research Associate, where you'll play a critical role in the execution of clinical trials for innovative diagnostics and medical devices. This remote position offers an opportunity to work with top researchers and institutions, emphasizing collaboration and continuous improvement. You will ensure compliance with regulatory standards while contributing to the advancement of healthcare solutions that save lives. Ideal candidates will have substantial clinical research experience, strong communication skills, and the ability to manage multiple projects effectively.
Posted 1 week ago
Senior Clinical Research Associate
RemotePrecision for Medicine is a unique CRO focusing on the oncology and rare disease sectors. They are looking for a Senior Clinical Research Associate to provide vital support to clinical research studies. The role includes overseeing study site management, ensuring patient safety, and maintaining data quality. Candidates should have at least 3 years of on-site monitoring experience, with a preferred background in oncology. Strong interpersonal skills and attention to detail are necessary, along with proficiency in Microsoft Office programs and the ability to work independently. Travel is required for this role.
Posted 1 week ago
Senior Clinical Research Associate
RemotePrecision for Medicine is looking for a Senior Clinical Research Associate to support clinical research studies in Oncology and Rare Disease. The role involves ensuring compliance with protocols and regulations, managing site operations, and maintaining high-quality data. The CRA will act as a liaison for study sites and clinical teams, requiring independent judgment and effective communication skills. Candidates should have a relevant degree and a minimum of 3 years of on-site monitoring experience. Familiarity with Microsoft Office and fluency in English are essential.
Posted 1 week ago
Senior Clinical Research Associate
RemotePSI CRO is seeking a Senior Clinical Research Associate to join our dynamic global team. This role involves communication with project stakeholders, ensuring clinical research projects meet standards and timelines. You will build relationships with clinical sites, focusing on subjects' rights and quality compliance. Candidates should possess relevant education, a minimum of five years of independent monitoring experience in the USA, and proficiency in English, among other skills. The position offers opportunities for career advancement within a company that prioritizes its employees.
Posted 2 weeks ago
Senior Clinical Research Associate
RemoteCareDx, Inc., a leader in precision medicine solutions for transplant patients, is seeking a Senior Clinical Research Associate for its Clinical Operations team. This crucial role focuses on the integrity, quality, and compliance of clinical trials. Candidates should have extensive experience in clinical study management and a commitment to enhancing patient outcomes. The position entails site visits, compliance with regulations, and mentoring junior CRAs. Successful applicants will exhibit strong analytical skills, a customer-focused mindset, and adaptability in a dynamic environment.
Posted 2 weeks ago
Clinical Trial Manager/ Senior Clinical Trial Manager
RemoteThe Clinical Trial Manager/Senior Clinical Trial Manager oversees the planning and execution of clinical studies, ensuring adherence to protocols and regulatory standards. This role involves collaborating with clients, developing crucial documentation, and managing study teams. The incumbent will also identify training needs for clinical research associates (CRAs), conduct feasibility analyses, and handle the logistics of investigator meetings. Ideal candidates should possess a minimum of seven years of clinical research experience and a strong educational background in a science or health-related field.
Posted 1 week ago
Clinical Trial Manager/Sr Clinical Trial Manager
RemoteErasca is seeking a Clinical Trial Manager or Senior Clinical Trial Manager to oversee global oncology clinical trials from planning through execution. The ideal candidate will have substantial experience in managing clinical vendors and ensuring compliance with regulatory standards. Responsibilities include site management, budget oversight, and providing updates to management. Candidates should have a life sciences degree and significant experience in trial operations with demonstrated leadership skills. The anticipated salary range is $145,000 to $190,000, along with a comprehensive benefits package.
Posted 1 week ago
Clinical Trial Manager
RemoteThe Clinical Trial Manager leads the execution of clinical studies and oversees data collection, ensuring adherence to clinical protocols. Responsibilities include providing strategic input on study documents, developing recruitment strategies, and managing compliance with regulations. With a minimum of 7 years in clinical operations, the manager collaborates with cross-functional teams and stakeholders. The position requires effective communication, decision-making skills, and involves light travel, offering a dynamic work environment focused on drug development.
Posted 6 days ago
Clinical Trial Manager
RemoteSyneos Health is seeking a Clinical Trial Manager dedicated to sponsor operations, requiring project management experience and previous CRA experience. This role involves overseeing clinical monitoring, ensuring compliance with protocols and regulations, and collaborating with various teams to achieve trial milestones. The Clinical Trial Manager will lead site management, risk assessment, and document quality. A Bachelor's degree or RN in a related field is essential, along with strong communication and conflict resolution skills. This position is remote, contributing to global drug development efforts.
Posted 1 week ago
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Remote Clinical Research Salary Data in June 2026
This section summarizes salary information from 3,624+ active remote clinical research job postings, including roles in clinical trial coordination, clinical research associate work, site monitoring, data review, and study operations. Use it to compare compensation patterns across remote clinical research roles before applying.
Average Salary
$101k
$129k
$160k
25th
50th
75th
Based on 3,624 roles currently tracked by LiftmyCV. Last updated on Jun 23, 2026
Salary Distribution
Based on 3,624 roles currently tracked by LiftmyCV. Last updated on Jun 23, 2026
| Experience Level | 25th Percentile | Median (50th) | 75th Percentile | Sample Size |
|---|---|---|---|---|
| Overall | $101,000 | $128,800 | $160,252.5 | 1,710 |
| Entry-Level | $62,250 | $67,000 | $76,750 | 4 |
| Mid-Level | $92,450 | $117,500 | $132,250 | 27 |
| Senior-Level | $129,850 | $166,102.5 | $195,710.88 | 24 |
"Remote clinical research hiring in 2026 tends to favor candidates who can prove they’ve already worked cleanly across sites, sponsors, CROs, EDC systems, and regulated documentation without daily in-person oversight. For CRAs, coordinators, data roles, and trial operations teams, the resume has to show protocol discipline, monitoring judgment, audit readiness, and comfort working across time zones. Remote access is attractive, but employers still screen hard for structure, accountability, and clean communication."
Marina's Market Take
Senior HR Leader & Lead Tech Recruiter
How to Land a Remote Clinical Research Job in 2026
Remote clinical research jobs usually reward candidates who can show that they understand trial execution without needing constant in-person oversight. For CRA, clinical trial associate, study coordinator, regulatory affairs, and clinical data roles, your application should make the remote piece practical: site communication, documentation discipline, protocol follow-through, and comfort working across CTMS, eTMF, EDC, and shared study trackers.
Start by choosing a clear lane. A remote CRA should emphasize monitoring visits, query follow-up, site training, adverse event documentation, and sponsor or CRO communication. A clinical trial coordinator or clinical research associate support candidate should point to patient scheduling, IRB submissions, consent workflows, study binders, and vendor coordination. Regulatory candidates need to foreground submissions, essential documents, protocol amendments, and audit-ready filing. Clinical data candidates should lead with EDC review, discrepancy management, data cleaning, and collaboration with biostatistics or medical review teams.
- Show the trial phase and therapeutic area when you can. Oncology, vaccines, cardiology, rare disease, or device studies tell employers more than a generic clinical research title.
- Make remote collaboration visible. Mention sponsor calls, site follow-ups, remote monitoring, document review cycles, and cross-functional work with CRAs, project managers, data teams, and regulatory staff.
- Use compliance language carefully. Reference GCP, ICH guidelines, SOPs, informed consent, protocol deviations, and audit readiness only where you have handled those responsibilities directly.
- Prioritize postings that match your operating level. Entry-level clinical trial assistant roles, mid-level CRA positions, and senior study management jobs ask for different evidence, even when all are listed as remote clinical research jobs.
For search strategy in 2026, filter for work style and trial function together, such as remote CRA, remote clinical trial coordinator, remote regulatory specialist, or remote clinical data associate. LiftmyCV helps you find remote clinical research jobs that match your skills, experience, and preferred work style, then auto-apply to relevant roles faster.
Required Skills
Resume Tips
For remote clinical research jobs, your resume should show that you can manage regulated study work without constant in-person supervision. Highlight experience with clinical trial documentation, study start-up, site monitoring, patient recruitment, protocol adherence, adverse event tracking, and communication with investigators, sponsors, CROs, or IRBs. If you have worked with EDC or CTMS tools, name them clearly, such as Medidata Rave, Veeva Vault, Oracle Clinical, REDCap, Florence, or TrialMaster. Certifications like CCRC, CCRP, ACRP-CP, GCP training, or ICH-GCP familiarity also belong near the top if they match the posting.
Cut vague healthcare language that does not connect to trial operations. A line like “Worked with patients and maintained records” is too broad for remote clinical research roles. Replace it with proof of study-specific work, compliance habits, and remote coordination.
- Weak: Assisted with clinical research tasks and updated study files.
- Strong: Coordinated remote site documentation for Phase II oncology studies, tracked queries in Medidata Rave, and maintained TMF records in Veeva Vault under ICH-GCP requirements.
Present older clinical care experience through a research lens. Nursing, pharmacy, lab, public health, or patient coordinator work can help if you connect it to informed consent, source documentation, protocol visits, safety reporting, data accuracy, or HIPAA-aware communication. For 2026 postings, remote readiness also matters, so mention virtual monitoring, eConsent workflows, video site check-ins, shared trackers, and cross-time-zone sponsor updates when they are real parts of your background.
How to Prepare for Interviews
Interviews for remote clinical research jobs often test how you manage protocol details, site communication, documentation, and deadlines without daily in-person supervision. Prepare examples from clinical trial coordination, CRA work, data review, regulatory support, patient recruitment, or vendor follow-up, depending on the roles you’re targeting in 2026.
Expect scenario questions such as, “A site is behind on query resolution and missing source documents. What do you do first?” A good answer should walk through prioritization, escalation, audit trail habits, and how you keep the PI, site staff, sponsor, or CRO team aligned. For clinical research coordinator and CRA-style roles, review GCP, informed consent, protocol deviation handling, monitoring visit reports, and EDC workflows. For remote trial operations or regulatory roles, prepare to discuss document tracking, IRB submissions, TMF quality, and cross-functional handoffs.
Bring concise examples with metrics where possible: enrollment targets, query turnaround time, number of sites supported, study phases, therapeutic areas, or inspection readiness work. Remote roles also call for clear examples of communication across time zones, disciplined follow-up, and careful documentation.