Remote Clinical Trial Manager Jobs
Remote clinical trial manager jobs are open across the U.S. at remote-first sponsors, contract research organizations, and distributed biotech and pharmaceutical teams. Companies hiring remotely right now include Parexel, ICON, and Menarini. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 31+ Remote Clinical Trial Manager jobs
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Location/Division Specific Information
Join Thermo Fisher Scientific as a Medical Director/Clinical Trial Physician(FSP) based in the United States and be part of a world-class organization conducting groundbreaking research. Ideal candidate location is Eastern or Central Time Zone. This position is fully remote, benefit eligible with travel in a 10-20% range(international maybe required).
- Must be legally authorized to work in the United States or Canada without sponsorship.
- Must be able to pass a comprehensive background check, which includes a drug screening(where applicable).
- East coast time zone is preferred, or ability to work EST hours
Client Dedicated Role:
Our client, a global mid-sized biotech company, focuses on developing innovative treatments for patients with autoimmune diseases. This fast-growing, international organization has a strong scientific foundation. If you're looking for a place where your work, in partnership with others, can have real impact—and where you're encouraged to challenge yourself and contribute to breakthrough solutions , the Medical Director/Clinical Trial Physician could be a great fit.
Discover Impactful Work:
Provides clear medical leadership in the Study team, working in close collaboration with the other members of this cross functional team, in order to provide reliable, high quality study data within time and budget.
A day in the Life:
Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active escalation and correction of issues in consultation with the Global Medical Indication Lead
Interpret the clinical trial data for regulatory documents (e.g. CSR, INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required, in consultation with the Indication Lead
Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
In case more than 1 physician is working on the protocol, a primus inter pares will be appointed, and they will ensure that answers to questions from sites /IRBs RAs, eligibility and protocol deviation decisions will be harmonized across medics
Keys to Success:
Education
Medical Doctor or equivalent degree required. Board certification(s) are preferred
Specialty education(e.g. residency/fellowship) required in neurology. This should be accompanied by patient treatment and/or research experience
1-3 years of industry experience required. Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization
Neurologists with expertise in Pediatric Neurology or Neuromuscular diseases are highly preferred.
Knowledge, Skills, Abilities
Excellent English, both written and spoken is a must, as well as ability to travel
Shown understanding and experience with NDA submission process
Shown understanding of regulatory guidelines for adverse event reporting
Proven interpersonal skills enabling to lead a study team, while recognizing individual expert competencies, providing medical advice and evaluations exercising judgment in which issues need to be escalated immediately
Pro-active problem solver with negotiation skills, remaining sensitive to the different cultural needs in a global organization
Strong communication skills to ensure close collaboration with the cross functional team members so that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties. A matrix structure requires additional skills in gathering decision information, negotiation and communicating decisions and actions
Physical Requirements / Work Environment
Work is performed in an office environment with exposure to electrical office equipment
Occasional drives to site locations with occasional travel both domestic and international
Frequently stationary for 6-8 hours per day
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists
Frequent mobility required
Occasional crouching, stooping, bending and twisting of upper body and neck
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences
Frequently interacts with others to obtain or relate information to diverse groups
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task
Regular and consistent attendance
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Location/Division Specific Information
Join Thermo Fisher Scientific as a Medical Director/Clinical Trial Physician(FSP) based in the United States and be part of a world-class organization conducting groundbreaking research. Ideal candidate location is Eastern or Central Time Zone. This position is fully remote, benefit eligible with travel in a 10-20% range(international maybe required).
- Must be legally authorized to work in the United States or Canada without sponsorship.
- Must be able to pass a comprehensive background check, which includes a drug screening(where applicable).
- East coast time zone is preferred, or ability to work EST hours
Client Dedicated Role:
Our client, a global mid-sized biotech company, focuses on developing innovative treatments for patients with autoimmune diseases. This fast-growing, international organization has a strong scientific foundation. If you're looking for a place where your work, in partnership with others, can have real impact—and where you're encouraged to challenge yourself and contribute to breakthrough solutions , the Medical Director/Clinical Trial Physician could be a great fit.
Discover Impactful Work:
Provides clear medical leadership in the Study team, working in close collaboration with the other members of this cross functional team, in order to provide reliable, high quality study data within time and budget.
A day in the Life:
Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active escalation and correction of issues in consultation with the Global Medical Indication Lead
Interpret the clinical trial data for regulatory documents (e.g. CSR, INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required, in consultation with the Indication Lead
Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
In case more than 1 physician is working on the protocol, a primus inter pares will be appointed, and they will ensure that answers to questions from sites /IRBs RAs, eligibility and protocol deviation decisions will be harmonized across medics
Keys to Success:
Education
Medical Doctor or equivalent degree required. Board certification(s) are preferred
Specialty education(e.g. residency/fellowship) required in neurology. This should be accompanied by patient treatment and/or research experience
1-3 years of industry experience required. Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization
Neurologists with expertise in Pediatric Neurology or Neuromuscular diseases are highly preferred.
Knowledge, Skills, Abilities
Excellent English, both written and spoken is a must, as well as ability to travel
Shown understanding and experience with NDA submission process
Shown understanding of regulatory guidelines for adverse event reporting
Proven interpersonal skills enabling to lead a study team, while recognizing individual expert competencies, providing medical advice and evaluations exercising judgment in which issues need to be escalated immediately
Pro-active problem solver with negotiation skills, remaining sensitive to the different cultural needs in a global organization
Strong communication skills to ensure close collaboration with the cross functional team members so that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties. A matrix structure requires additional skills in gathering decision information, negotiation and communicating decisions and actions
Physical Requirements / Work Environment
Work is performed in an office environment with exposure to electrical office equipment
Occasional drives to site locations with occasional travel both domestic and international
Frequently stationary for 6-8 hours per day
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists
Frequent mobility required
Occasional crouching, stooping, bending and twisting of upper body and neck
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences
Frequently interacts with others to obtain or relate information to diverse groups
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task
Regular and consistent attendance
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
See All 31 Remote Clinical Trial Manager Jobs
Find roles that match your experience and apply in just a few clicks.
Find JobsRemote Clinical Trial Manager Job Market
Who's Hiring
Top Industries Hiring
- Education
- Science & Research
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What Employers Look For
The qualifications that appear most often in remote clinical trial manager jobs.
- Bachelor's or advanced degree in life sciences, nursing, or a related clinical field
- 3-5 years of clinical trial management or clinical research associate experience
- ICH E6 Good Clinical Practice certification or equivalent documented training
- Proficiency with clinical trial management systems such as Veeva Vault or Medidata Rave
- Experience managing investigative sites across Phase II, III, or IV studies
- Strong working knowledge of FDA regulations and applicable regulatory guidelines
Tips for Your Remote Clinical Trial Manager Job Search
Apply early to remote roles that fit
Migrate Mate lists remote clinical trial manager openings from across the U.S. in one place, so you can find roles that match your experience and apply directly without sifting through unrelated postings.
Show remote site management experience clearly
Remote employers want to know you've managed clinical sites without being on-site. Specify in your application materials the number of sites you've overseen remotely, the therapeutic areas covered, and how you kept enrollment on schedule using virtual check-ins and electronic data capture tools.
Demonstrate async communication skills upfront
Remote clinical trial manager roles run on written updates, audit trails, and documented decision-making. Use your cover letter and any work samples to show you communicate protocol deviations, site issues, and milestone updates clearly in writing, because remote hiring managers judge async fluency before the interview.
Prepare for remote-specific interview scenarios
Expect interview questions about how you've handled a site going off-protocol when you couldn't visit in person, or how you escalated a vendor issue across time zones. Frame answers around the tools you used, the documentation you created, and how you kept the trial on track without physical presence.
Remote Clinical Trial Manager Jobs: Frequently Asked Questions
How do I get a remote clinical trial manager job?
Target remote-first contract research organizations, virtual biotech startups, and pharmaceutical companies with distributed clinical operations teams, as these employers are most likely to have built workflows that support remote trial managers. Remote employers screen for self-directed communication, rigorous documentation habits, and confidence managing sites, vendors, and data across time zones without in-person oversight. Proficiency with electronic data capture platforms and strong asynchronous writing skills give candidates a clear edge.
Which companies hire remote clinical trial managers?
Remote clinical trial manager roles are posted by Parexel, ICON, and Menarini and others right now, based on current remote listings on Migrate Mate as of September 2026. Hiring tends to concentrate at remote-first contract research organizations, distributed biotech firms, and pharmaceutical sponsors that have moved clinical operations to fully virtual or hybrid models.
Can you get a remote clinical trial manager job with no experience?
Yes, but remote entry-level clinical trial manager roles are harder to land because employers expect you to manage timelines and site relationships independently from day one. Contract research organizations and smaller virtual sponsors are most likely to hire at the entry level. Demonstrating clinical research coordinator experience, familiarity with Good Clinical Practice guidelines, and comfort with remote collaboration tools can open the door when direct management experience is thin.
Do you need a degree for remote clinical trial manager jobs?
Usually, but the field increasingly weighs hands-on clinical research experience alongside or instead of a specific degree. A background as a clinical research coordinator, proficiency with regulatory submissions, and demonstrated site management results can offset the absence of a life sciences degree at many remote employers, particularly at contract research organizations and smaller biotech sponsors looking for proven operators over credentialed newcomers.
Which industries hire the most remote clinical trial managers?
Most remote clinical trial manager openings sit in Education, Science & Research, and Biotechnology & Pharmaceuticals, per current remote listings on Migrate Mate as of September 2026. Those sectors rely on distributed clinical operations teams that coordinate sites, investigators, and vendors across geographies, making remote clinical trial management a natural fit for their operating models.
See All 31 Remote Clinical Trial Manager Jobs
Find roles that match your experience and apply in just a few clicks.
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