# 1,438 Remote Clinical Research Jobs (September 2026) > Browse verified remote clinical research jobs. Explore 1,438 active roles updated daily. Apply in one click with the LiftmyCV AI Agent. Canonical HTML: https://www.liftmycv.com/jobs/remote-clinical-research-jobs/ Markdown: https://www.liftmycv.com/jobs/remote-clinical-research-jobs.md Site: https://www.liftmycv.com/ 1,438 Remote Clinical Research Jobs (September 2026) Remote clinical research jobs in September 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. ## Expert Marina Galkina, Senior HR Manager, Lead Tech Recruiter, and Career Consultant https://www.linkedin.com/in/marina-galkina-148b93224/ "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. 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. 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. ## Remote Clinical Research Salary Data in September 2026 This section summarizes salary information from 1,438+ 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. | Level | P25 | P50 | P75 | | --- | --- | --- | --- | | Average | 102330.25 | 145000 | 166525 | | Entry | 52406.5 | 62400 | 76150 | | Mid | 85250 | 110000 | 130950 | | Senior | 143725 | 152500 | 183125 | Skills: ["clinical trials","GCP","study protocols","site monitoring","regulatory documentation","clinical data","patient recruitment","informed consent","source documentation","trial coordination","IRB submissions","adverse events","TMF management","EDC systems","quality assurance","remote monitoring","documentation","remote collaboration"] ## Example jobs - **Senior Clinical Research Associate (CRA) — MapLight Therapeutics — Remote**: MapLight Therapeutics is seeking a Senior Clinical Research Associate who will focus on quality Investigator site monitoring and management in the clinical trial industry. The position requires managing relationships with investigators while ensuring compliance with regulatory standards. Key responsibilities include site visits, centralized monitoring, and collaboration with internal and external teams. Candidates should possess extensive experience in CNS and neuropsychiatry trials. This remote role requires significant travel and a strong understanding of Good Clinical Practices (GCP). Competitive compensation and benefits are provided. - **Senior Clinical Research Associate — Precision for Medicine — Remote, Spain, Remote, United Kingdom, Remote, Poland, Remote, Germany, Remote, France, Remote, Hungary**: Precision for Medicine is seeking a Senior Clinical Research Associate to join their team to support dedicated FSP partnerships in Spain. This role is part of an evergreen posting aimed at building a talent pipeline for future needs. Candidates will monitor clinical studies, ensure compliance with regulations, and interact with clients while mentoring junior staff. Preferred qualifications include a minimum of five years of CRA experience in various environments with fluency in Spanish and English. Precision for Medicine values agility and collaboration, offering professional development opportunities. - **Senior Clinical Research Associate — Precision Medicine Group — Remote, Spain, Remote, United Kingdom, Remote, Poland, Remote, Hungary, Remote, France, Remote, Germany**: Precision Medicine Group is seeking a Senior Clinical Research Associate for future opportunities in Spain. This role involves monitoring clinical studies, coordinating necessary activities for study setup, and mentoring junior staff. Candidates should have a minimum of five years of CRA/SCRA experience, especially in IVD, oncology, and infectious disease studies across Europe. This is an evergreen posting aimed at building a talent pipeline for upcoming projects, offering a fully home-based opportunity. Fluency in Spanish and English is required. - **Senior Clinical Research Associate — Karius — Redwood City, CA (Hybrid) or Remote (United States)**: Karius is seeking a Senior Clinical Research Associate to lead advanced clinical site management and monitoring for its clinical programs. This role involves ensuring adherence to protocols and guidelines while managing complex sites, monitoring findings, and mentoring junior team members. The successful candidate will utilize Karius' innovative diagnostics to impact patient care significantly. The company leverages genomics and AI to enhance diagnostic insights and improve treatment outcomes for infectious diseases, making this an exciting opportunity to be part of a transformative field. - **Senior Clinical Research Associate — Parexel International, LLC — United States - Remote**: **When our values align, there's no limit to what we can achieve.** At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. PXL FSP has an exciting opportunity for a Senior CRA ! **The Senior Clinical Research Associate is responsible for the following: ** *Act as the primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.* **Key Accountabilities:** **Site Management Responsibilities** - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. - Gains an in-depth understanding of the study protocol and related procedures. - Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready. - Participates & provides inputs on site selection and validation activities. - Performs remote and on-site monitoring & oversight activities using various tools to ensure: - Data generated at site are complete, accurate and unbiased. - Subjects’ right, safety and well-being are protected. - Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. - Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out. - Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance. - Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA-Manager, CRM, TA Head and CRD as needed. - Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites. - Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines. **Team Development and Support** - Contributes strongly to CRA team knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required. - Supports and/or leads audit/inspection activities as needed. - Mentors / buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate. - Contributes to initiatives and projects adding value to the business - Performs co-monitoring as appropriate **Compliance with Parexel Standards ** • Comply with required training curriculum • Complete timesheets accurately as required • Submit expense reports as required • Update CV as required • Maintain a working knowledge of and complies with Parexel/Client processes, ICH-GCPs and other applicable requirements **Skills:** • Fluent in local languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively • Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP / ICH and country clinical research law and guidelines • Hands on knowledge of Good Documentation Practices • Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines • Demonstrated ability to mentor/lead • Proven skills in Site Management including independent management of site performance and patient recruitment • Demonstrated high level of monitoring skill with independent professional judgement • Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices • Ability to understand and analyze data/metrics and act appropriately • Experience with conducting site motivational visit designed to boost site enrollment • Capable of managing complex issues, works in a solution-oriented manner • Performs root cause analysis and implements preventative and corrective action • Capable of mentoring junior CRAs on process/study requirements and is able to perform co-monitoring visits where appropriate • Effective time management, organizational and interpersonal skills, conflict management, problem solving skills • Able to work highly independently across multiple protocols, sites, and therapy areas • High sense of accountability / urgency • Ability to set priorities and handle multiple tasks simultaneously in a changing environment • Works effectively in a matrix multicultural environment; ability to establish and maintain culturally sensitive working relationships • Demonstrates commitment to customer focus • Works with high quality and compliance mindset • Positive mindset, growth mindset, capable of working independently and being self-driven • Demonstrates and projects professional demeanor and communication consistent with organizational policies and practices • Ability to travel domestically and internationally approximately 65%-75% of working time • Expected travelling ~2-3 days/week • Current driver’s license required **Knowledge and Experience:** • Minimum 4 years of direct site management (monitoring) experience in bio/pharma/CRO Note: Specific monitoring or therapeutic experience/requirements may vary depending on the Country or study needs **Education:** • Bachelor’s degree preferred with a strong emphasis in science and /or biology #LI-KW1 **EEO Disclaimer** Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. - **Senior Clinical Research Associate — WCT Clinical Research Spain, S.L. — Barcelona, Spain**: Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to join their dynamic team. This role focuses on site qualification, initiation, monitoring, management, and study close-out visits. The ideal candidate will bring over 5 years of experience and possess excellent communication and organizational skills. Worldwide emphasizes a diverse and inclusive environment, empowering team members to excel while making a meaningful impact in clinical research. Join a company devoted to innovation and creativity in the pursuit of better patient outcomes. - **Senior Clinical Research Associate — Parexel International Turkey — Turkey-Remote**: Parexel seeks a Senior Clinical Research Associate on a temporary contract to oversee clinical trial monitoring and ensure compliance with relevant regulations. The role involves working closely with investigator sites throughout the trial process, addressing recruitment and monitoring needs. Candidates should have extensive knowledge of clinical trial methodologies, a minimum of three years of monitoring experience, and be fluent in English. This remote position offers an opportunity to contribute to patient-focused clinical trials and drive innovation in clinical research. - **Senior Clinical Research Associate — Pulse Biosciences — United States Remote**: Join Pulse Biosciences, a forward-thinking bioelectric medicine company focused on improving patient care through innovative technology. As a Senior Clinical Research Associate (Sr. CRA), you will manage and monitor clinical studies, ensuring compliance with regulations and promoting high-quality outcomes. You will collaborate with various stakeholders while contributing to a dynamic, startup-like environment that values creativity, growth, and diversity. This role offers significant responsibilities in guiding research activities and mentoring fellow associates, all while balancing work-life commitments. - **Senior Clinical Research Associate — Syneos Health UK Limited — GBR-Remote**: Syneos Health is seeking a Senior Clinical Research Associate with UK on-site monitoring experience. This remote position involves collaborating with a dedicated Clinical Solutions team to ensure compliance throughout the drug development process. Responsibilities include site qualification, data accuracy verification, and project management. This role demands excellent communication skills and a proactive approach to problem-solving. Join a company recognized for its commitment to career development and an inclusive culture focused on delivering impactful healthcare solutions. - **Senior Clinical Research Associate — ProTrials Research, Inc. — Regional**: ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries. Our people are the heart of everything we do. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you’ll join a collaborative community committed to making a meaningful impact on global health. We are excited to connect with skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence. ABOUT THE JOB The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. Sr. CRAs may be required to travel up to 65%. ABOUT THE JOB The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. Sr. CRAs may be required to travel up to 65%. ### HERE IS WHAT YOU WILL DO: Monitor clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit, including qualification, initiation, interim, and close-out site visits Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion Manage and track the preparation and return of investigational supplies at individual sites Monitor and document investigational product dispensing, inventory, and reconciliation Monitor and document laboratory sample storage and shipment Monitor trial by reviewing and reporting on the following: site enrollment and termination updates, monitoring visits, protocol deviations/exceptions, serious adverse events, and laboratory abnormalities Review source data and case report forms for accuracy, completeness, and integrity of the data, and identify and resolve ongoing data issues Review data queries and listings, and work with study centers to resolve data discrepancies Review regulatory documentation for accuracy and completeness, and support study centers with regulatory issues Maintain complete and accurate study files and review files to ensure all appropriate documentation is present Maintain consistent and timely contact with the study centers, investigators, coordinators, client personnel, and other individuals involved in clinical trials Serve as a resource for project team members including supporting CRA I and CRA II staff by providing solutions to resolve issues ### HERE IS WHAT YOU BRING TO THE TABLE: RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and previous CRA experience demonstrating career growth in the CRA position Detail-oriented Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills Flexibility with changing priorities Ability to efficiently perform and prioritize multiple tasks Familiarity with the medical and pharmaceutical industries, and related terminology and practices Extensive knowledge of FDA regulations and their practical implementation Ability to travel, including by air or by car on short notice Proficiency in Microsoft Word, Excel, and PowerPoint ### HERE IS WHAT WE OFFER: Your wellness matters to us – that’s why we provide full medical, dental, and vision insurance options for you and your family. We know life doesn’t pause for work – we provide flexible PTO so you can take care of what matters, both personally and professionally. You invest in your future – and so do we. Our 401(k) plan includes a company match to help you reach your financial goals. At ProTrials, we are committed to your growth. Whether you’re looking to expand your skills or take the next step in your career, we provide the support and opportunities you need to keep moving forward. We have the best coworkers, if we do say so ourselves. Except as otherwise permitted or required by applicable law or regulatory requirements, ProTrials will retain the applicant’s personal information in accordance with its statutory obligations and internal policies and procedures. Information collected during application completion may be retained for a reasonable period of time and in accordance with the company’s established retention policies. Applicants seeking more information may contact [HR@ProTrials.com](mailto:HR@ProTrials.com). ProTrials is an equal opportunity employer. ProTrials is committed to providing a workplace free from discrimination and harassment. All qualified candidates will receive equal consideration for employment without regard to race, color, citizenship status, national origin, ancestry, gender (including gender identity and gender expression), pregnancy, and childbirth or related medical conditions (including genetic characteristics), genetic information, sexual orientation, age, religion, creed, physical or mental disability, medical condition, military or veteran status, marital status, political affiliation, or any other characteristic protected by state or federal law. - **Senior Clinical Research Associate — Parexel International (Canada) LTD — Canada-British Columbia-Remote**: The Senior Clinical Research Associate (Sr. CRA) at Parexel is pivotal in managing and monitoring clinical trial sites to ensure patient safety and quality compliance. The role involves liaising with site staff, overseeing operational aspects of clinical trials, and ensuring adherence to Good Clinical Practices (GCP). A focus on investigator relationships is essential for effective trial delivery, along with problem-solving for any protocol-related issues. Candidates should have a strong background in clinical research methodologies and be prepared for significant travel. A bachelor's degree in life sciences is required. - **Senior Clinical Research Associate — Worldwide Clinical Trials Holdings, Inc. — Research Triangle Park, North Carolina**: Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to join their innovative and diverse team. This remote role focuses on managing research activities across various therapeutic areas, especially oncology, while supporting site compliance and regulatory requirements. Candidates should possess strong communication and organizational skills, with at least 5 years of experience in clinical research. Join a company dedicated to improving lives through collaborative and pioneering research efforts. ## Related - [Clinical Research Associate Jobs](/jobs/clinical-research-associate-jobs/) - [Remote Healthcare Jobs](/jobs/remote-healthcare-jobs/) - [Healthcare Jobs](/jobs/healthcare-jobs/) - [Remote Healthcare Administration Jobs](/jobs/remote-healthcare-administration-jobs/) - [Healthcare Administration Jobs](/jobs/healthcare-administration-jobs/) - [Remote Nursing Jobs](/jobs/remote-nursing-jobs/) - [Remote Case Manager Jobs](/jobs/remote-case-manager-jobs/) - [Case Manager Jobs](/jobs/case-manager-jobs/) - [Remote Data Analyst Jobs](/jobs/remote-data-analyst-jobs/) - [Data Analyst Jobs](/jobs/data-analyst-jobs/) - [Remote QA (Quality Assurance) Jobs](/jobs/remote-qa-jobs/) - [Remote Jobs in the US](/jobs/remote-jobs-us/) ## FAQ ### Can clinical research jobs be fully remote? Remote clinical research jobs can be fully remote, hybrid, or remote-first based on how the employer handles study work. Some clinical research tasks can be done online, while other positions may still require site contact, scheduled meetings, or occasional travel. Read each listing closely for workplace language before applying in 2026. ### What should I look for in a remote clinical research job posting? For remote clinical research jobs, check the posting for study responsibilities, communication expectations, location restrictions, and any required availability during business hours. A remote label alone may not explain whether the role involves trial documentation, study coordination, sponsor communication, or site support. The details matter more than the headline. ### Are remote clinical research jobs good for people without on-site experience? Some remote clinical research jobs may be open to applicants who can show careful documentation habits, healthcare exposure, or research-related coursework. Others may expect prior clinical research experience before allowing remote work. Since the page focuses on remote clinical research jobs, compare requirements line by line rather than assuming every listing is entry-level. ### How do I apply for remote clinical research jobs in September 2026? When applying for remote clinical research jobs in September 2026, focus your resume on clinical research tasks, remote collaboration, documentation accuracy, and any study-related responsibilities you’ve handled. If a posting mentions specific trial work or research coordination, mirror that language honestly. LiftmyCV can help organize those details without turning the application into generic remote-work copy. ### Do remote clinical research jobs require travel? Some remote clinical research jobs may still include travel, site visits, or occasional in-person meetings, even when the main workplace is remote. The listing should explain whether travel is expected and how often it may happen. If the posting is vague, ask before investing too much time in the application process. ### What experience matters most for remote clinical research jobs? Remote clinical research employers usually care about evidence that you can handle regulated, detail-heavy research work without constant in-person supervision. Useful anchors can include clinical research exposure, study documentation, patient or site communication, and organized follow-through. Keep the resume tied to clinical research rather than describing only general remote office experience. ### Apply to Remote Clinical Research Jobs Faster Use LiftmyCV to match with remote clinical research openings, tailor your resume for each role, and auto-apply without repeating the same application steps.