Remote Clinical Research Associate Jobs
Remote clinical research associate jobs are in active demand across the U.S., with remote-first firms and distributed clinical operations teams hiring for site monitoring, data oversight, and trial management work. Employers hiring remotely right now include CVS Health, Medpace, and Alvarez & Marsal. See the openings below and apply to the ones that match your experience.
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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 Associate Job Market
Who's Hiring
- CVS Health30
- Medpace27
- Alvarez & Marsal26
- Worldwide Clinical Trials13
- サイネオス・ヘルス11サ
Top Industries Hiring
- Technology & Software60
- Healthcare & Medical Services51
- Biotechnology & Pharmaceuticals42
- Consulting & Professional Services42
- Science & Research34
What Employers Look For
The qualifications that appear most often in remote clinical research associate jobs.
- Bachelor's degree in life sciences, nursing, or a related clinical field
- ICH E6(R2) Good Clinical Practice certification or equivalent training
- Experience conducting site initiation, interim monitoring, and close-out visits
- Proficiency with electronic data capture systems such as Medidata Rave or Oracle InForm
- Knowledge of FDA regulations, including 21 CFR Parts 11, 50, and 56
- Ability to manage multiple investigative sites concurrently across geographies
Tips for Your Remote Clinical Research Associate Job Search
Apply early to remote roles that fit
Migrate Mate lists remote clinical research associate openings from across the U.S. in one place. Search roles by therapeutic area or monitoring type and apply directly to the ones that match your protocol experience before postings fill.
Show remote monitoring capability upfront
Name the electronic data capture systems you've used, such as Medidata Rave, Veeva Vault, or Oracle Clinical One, in your resume and cover letter. Remote employers need to know you can conduct source data verification and site oversight without traveling.
Demonstrate async communication in interviews
Remote clinical operations teams rely on written updates, structured emails, and clear monitoring visit reports. During interviews, reference specific examples of how you've communicated site issues, protocol deviations, or escalations in writing with sponsors or sites.
Target decentralized and hybrid trial sponsors
Sponsors running decentralized clinical trials and contract research organizations with remote monitoring programs hire clinical research associates remotely most consistently. Focus your search on companies that describe hybrid or fully remote monitoring in their job postings.
Prepare for remote onboarding from day one
Remote clinical research associate roles often assign sites immediately after onboarding. Before your start date, confirm access to the sponsor's electronic trial master file system, review the protocol and monitoring plan, and establish your communication cadence with site coordinators.
Remote Clinical Research Associate Jobs: Frequently Asked Questions
How do I get a remote clinical research associate job?
Target companies with distributed clinical operations teams, including contract research organizations with remote monitoring programs and sponsors running decentralized trials. Remote employers screen for strong written communication, comfort with electronic data capture systems, and the ability to manage site relationships without in-person visits. Demonstrating self-direction through independent monitoring experience and proficiency with remote source data verification gives candidates a clear edge.
Which companies hire remote clinical research associates?
Employers currently hiring remote clinical research associates include CVS Health, Medpace, and Alvarez & Marsal, per current remote listings on Migrate Mate as of June 2026. Contract research organizations, biopharmaceutical sponsors, and medical device companies with decentralized or hybrid trial models are the most consistent sources of remote clinical research associate openings.
Can you get a remote clinical research associate job with no experience?
Yes, but remote entry-level roles are harder to land because you're expected to manage sites and solve problems independently from day one. Contract research organizations occasionally hire remote clinical research assistants or junior monitors who train remotely. Showing familiarity with Good Clinical Practice guidelines, electronic data capture platforms, and strong written communication skills can open doors when direct monitoring experience is limited.
Do you need a degree for remote clinical research associate jobs?
Usually, but the field weighs practical credentials alongside formal education. Most remote employers expect a life sciences degree or equivalent clinical background, though relevant certifications like the SOCRA CCRP or ACRP CCRC can strengthen a profile. Remote employers also put significant weight on demonstrated experience with site management, protocol adherence, and the written communication skills that remote monitoring depends on.
Which industries hire the most remote clinical research associates?
Most remote clinical research associate openings sit in Technology & Software, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, per current remote listings on Migrate Mate as of June 2026. These sectors rely on distributed clinical teams to manage geographically spread trial sites without requiring associates to be co-located with sponsors or sites.
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