Remote Clinical Research Manager Jobs
Remote Clinical Research Manager jobs are open across the U.S. in pharmaceuticals, biotechnology, contract research organizations, and medical device companies, from mid-level managers stepping into distributed teams to senior leaders overseeing multi-site trials. Employers hiring remotely right now include Medpace, CVS Health, and Alvarez & Marsal. Scan the live roles below and apply to whichever ones fit.
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INTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
ROLE AND RESPONSIBILITIES
SystImmune is seeking a high quality, ambitious and experienced Senior Clinical Research Associate (CRA) to support SystImmune’s clinical trials. The Sr. CRA is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. The Sr CRA must be self-motivated, independent, and able to work in a small team environment. The successful candidate will be a highly organized individual who can also multitask and adjust direction based on changing project/corporate priorities.
- Perform Site Evaluation Visits, Site Initiation Visits, Interim monitoring visits and Close Out Visits.
- Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites.
- Responsible for ensuring investigator sites have met all contractual and regulatory requirements for site initiation and first release of study drug.
- Assist in the development of study/program plans (i.e., Monitoring Plan, eCRF Completion Guidelines, Data Management Plan, Safety Management Plan, etc.).
- Manage patient recruitment strategies, proactively identifying barriers to recruitment while proposing solutions (i.e., study-site webinars, newsletters or other potential creative solutions).
- Monitor recruitment, data quality and patient safety while on site and remotely through EDC systems and direct site communication.
- Liaise with study site personnel to ensure timely and correct entry of data into eCRF, including the timely resolution of data queries.
- Maintain project files including ethics committee approvals, curricula vitae of investigators and study personnel, clinical investigators brochure, protocols, case report forms instructions, consent documents, clinical-trial material shipping orders, start-up meeting attendance documentation, letters of agreement, lab reference ranges, and all investigator and site correspondence.
- Identify and complete follow-up of SAEs at study sites.
- Assist with data listing, data coding, patient profile reviews, database lock, and site close-out activities.
- Ensure appropriate and timely submission of documents to the Trial Master File.
- Perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP.
BASIC QUALIFICATIONS
- Bachelor’s degree in health science or related field.
- 5+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits.
- Excellent verbal and written communication skills required.
- Excellent organizational, multi-tasking and time management skills required.
- Demonstrated experience developing/maintaining site relationships and securing compliance.
- Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines.
- Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
- Ability to travel as required (50-75%).
COMPENSATION AND BENEFITS
The expected base salary range for this position is $90,000 - $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
INTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
ROLE AND RESPONSIBILITIES
SystImmune is seeking a high quality, ambitious and experienced Senior Clinical Research Associate (CRA) to support SystImmune’s clinical trials. The Sr. CRA is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. The Sr CRA must be self-motivated, independent, and able to work in a small team environment. The successful candidate will be a highly organized individual who can also multitask and adjust direction based on changing project/corporate priorities.
- Perform Site Evaluation Visits, Site Initiation Visits, Interim monitoring visits and Close Out Visits.
- Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites.
- Responsible for ensuring investigator sites have met all contractual and regulatory requirements for site initiation and first release of study drug.
- Assist in the development of study/program plans (i.e., Monitoring Plan, eCRF Completion Guidelines, Data Management Plan, Safety Management Plan, etc.).
- Manage patient recruitment strategies, proactively identifying barriers to recruitment while proposing solutions (i.e., study-site webinars, newsletters or other potential creative solutions).
- Monitor recruitment, data quality and patient safety while on site and remotely through EDC systems and direct site communication.
- Liaise with study site personnel to ensure timely and correct entry of data into eCRF, including the timely resolution of data queries.
- Maintain project files including ethics committee approvals, curricula vitae of investigators and study personnel, clinical investigators brochure, protocols, case report forms instructions, consent documents, clinical-trial material shipping orders, start-up meeting attendance documentation, letters of agreement, lab reference ranges, and all investigator and site correspondence.
- Identify and complete follow-up of SAEs at study sites.
- Assist with data listing, data coding, patient profile reviews, database lock, and site close-out activities.
- Ensure appropriate and timely submission of documents to the Trial Master File.
- Perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP.
BASIC QUALIFICATIONS
- Bachelor’s degree in health science or related field.
- 5+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits.
- Excellent verbal and written communication skills required.
- Excellent organizational, multi-tasking and time management skills required.
- Demonstrated experience developing/maintaining site relationships and securing compliance.
- Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines.
- Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
- Ability to travel as required (50-75%).
COMPENSATION AND BENEFITS
The expected base salary range for this position is $90,000 - $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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Find JobsRemote Clinical Research Manager Job Market
Who's Hiring
- Medpace32
- CVS Health32
- Alvarez & Marsal26
- Worldwide Clinical Trials13
- サイネオス・ヘルス11サ
Top Industries Hiring
- Technology & Software67
- Healthcare & Medical Services65
- Biotechnology & Pharmaceuticals49
- Consulting & Professional Services44
- Science & Research37
What Employers Look For
The qualifications that appear most often in remote clinical research manager jobs.
- Bachelor's or master's degree in life sciences, nursing, or a related clinical field
- Minimum of five years of clinical research experience including direct trial management
- Demonstrated knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Experience managing CRAs, site coordinators, or cross-functional study teams
- Proficiency with electronic data capture systems such as Medidata Rave or Veeva Vault
- Project Management Professional or SOCRA CCRP certification preferred by many employers
Tips for Your Remote Clinical Research Manager Job Search
Apply early to remote roles that fit
Migrate Mate lists remote clinical research manager openings from across the U.S. in one place, so you can find roles that match your therapeutic area and seniority and apply directly without sorting through unrelated listings.
Document your independent trial management
Remote employers want proof you've closed protocol deviations, managed CRAs, and kept enrollment on track without daily in-person support. Build a one-page summary of trials you've managed and the outcomes you drove, and reference it in applications.
Show mastery of remote clinical tools
Fluency with electronic data capture systems, CTMS platforms, and video-based site visit workflows signals to remote hiring managers that you can operate from day one. Name the specific systems you've used in your resume and cover materials.
Prepare for async-heavy remote interviews
Distributed clinical teams often screen with written case exercises or asynchronous video responses before live interviews. Practice explaining a site performance issue or a protocol deviation decision in writing as clearly as you would in person.
Target companies with decentralized trial programs
Organizations running decentralized or hybrid trials have embedded infrastructure for remote management and hire clinical research managers remotely as a standard practice, not an exception. Focusing your search on these companies increases your chances of landing a fully remote role.
Remote Clinical Research Manager Jobs: Frequently Asked Questions
How do I get a remote clinical research manager job?
Target employers that already run distributed clinical operations, such as contract research organizations, virtual biotech startups, and large pharma companies with decentralized trial programs. Remote hiring managers screen for self-direction, clear async written communication, and hands-on experience managing CRAs or study timelines without daily in-person oversight. Candidates who can show they've closed protocol deviations or kept site enrollment on track independently tend to move faster through remote processes.
Which companies hire remote clinical research managers?
Companies hiring remote clinical research managers right now include Medpace, CVS Health, and Alvarez & Marsal, based on current remote listings on Migrate Mate as of June 2026. Remote openings in this role are most common at contract research organizations, decentralized trial platforms, and mid-to-large biopharmaceutical companies that run distributed site networks.
Can you get a remote clinical research manager job with no experience?
Yes, but remote entry into this specific role is harder because remote employers expect you to manage study sites and vendors with limited hand-holding from day one. CROs and decentralized trial companies occasionally hire clinical research managers at an entry level if you can show clinical monitoring experience, a working knowledge of GCP, and documented examples of independent problem-solving on a trial. Contract or part-time remote roles at smaller biotech firms are often the most accessible starting point.
Do you need a degree for remote clinical research manager jobs?
Usually, but the degree matters less than your clinical trial experience and demonstrated ability to manage remotely. Most remote employers expect at least a bachelor's degree in a life sciences field, but candidates with strong CRA or study coordinator backgrounds, GCP certification, and a portfolio of trials they've managed end-to-end regularly advance past candidates with degrees and less hands-on experience.
Which industries hire the most remote clinical research managers?
The sectors hiring the most remote clinical research managers are Technology & Software, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, based on current remote listings on Migrate Mate as of June 2026. Those sectors rely on distributed site networks and decentralized trial models that make remote management a practical and common arrangement rather than an exception.
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