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Remote Medical Monitor Clinical Trial Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... remote patient monitoring and any/all decentralized trial processes * Tracks, monitors and reports ...

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · Remote

... site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry ... Working knowledge of medical terminology. * Experience with medical laboratory testing and ...

CTI

Clinical Trial Manager

Covington, KY · Remote

May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ... Ability to understand complex medical terminology and procedures * Ability to review and explain ...

CTI

Clinical Trial Manager

Covington, KY · On-site +1

May conduct on-site or remote monitoring activities as needed, including, but not limited to, Pre ... Ability to understand complex medical terminology and procedures * Ability to review and explain ...

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

Review protocol deviations and monitor for trends. * Coordinate review of data listings and ... Must be familiar with routine medical/scientific terminology * Knowledge of FDA and/or EMEA ...

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Remote Medical Monitor Clinical Trial information

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How much do remote medical monitor clinical trial jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for remote medical monitor clinical trial in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Remote Medical Monitor Clinical Trial vs Remote Clinical Research Coordinator?

AspectRemote Medical Monitor Clinical TrialRemote Clinical Research Coordinator
CredentialsMedical degree or clinical background, certifications like CCRP or CCRA often preferredBachelor's degree, often in health or science fields; certifications like CCRP beneficial
Work EnvironmentPrimarily remote, overseeing trial safety and complianceRemote or on-site, managing study logistics and participant coordination
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, CROs

The Remote Medical Monitor Clinical Trial focuses on overseeing patient safety and trial compliance remotely, often requiring clinical credentials. In contrast, the Remote Clinical Research Coordinator manages study logistics and participant coordination, with a broader range of educational backgrounds. Both roles are essential in clinical research but differ in responsibilities and required qualifications.

More about Remote Medical Monitor Clinical Trial jobs
What cities are hiring for Remote Medical Monitor Clinical Trial jobs? Cities with the most Remote Medical Monitor Clinical Trial job openings:
What are the most commonly searched types of Medical Monitor Clinical Trial jobs? The most popular types of Medical Monitor Clinical Trial jobs are:
What states have the most Remote Medical Monitor Clinical Trial jobs? States with the most job openings for Remote Medical Monitor Clinical Trial jobs include:
What job categories do people searching Remote Medical Monitor Clinical Trial jobs look for? The top searched job categories for Remote Medical Monitor Clinical Trial jobs are:
Remote Medical Monitor Clinical Trial jobs near you
Infographic showing various Remote Medical Monitor Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Senior Clinical Trial Manager

ARTBIO

Cambridge, MA • On-site, Remote

Full-time

Re-posted 14 days ago

Job description

SummaryThe Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial, and support the program strategy in a highly collaborative environment. The successful candidate will manage members of the clinical operations team, including those at CROs and study vendors, work collaboratively with clinical trial sites, and partner with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in line with regulatory requirements. The successful candidate must be comfortable working independently and cross-functionally to ensure study compliance and data quality.
Responsibilities
  • Lead cross-functional meetings with the Clinical Development, Clinical Operations, Data Management, regulatory, Quality, and Clinical Supply Chain.
  • Support the development within budget and on schedule.
  • Drive study startup activities, including feasibility, site selection, and timelines.
  • Manage activities of Phase 1 and 2 clinical trial investigators with a focus on the US to ensure compliance with the study protocol and overall clinical objectives.
  • Maintain clear communication across all departments.
  • Proactively manage, identify, and mitigate risks with the study team.
  • Serve as cross-functional lead for the clinical trial.
  • Identify and report potential program issues and implement CAPAs where necessary.
  • Act as the primary point of contact for trial execution and escalation.
  • Provide financial and management accountability updates to internal stakeholders as required.
  • Lead the oversight of CROs and vendors in partnership with the rest of the Clinical Operations team to assure the integrity of clinical data with respect to accuracy, accountability, and documentation through review of case report forms, source documents, medical records, etc.
  • Perform clinical research site activities, which can include onsite or remote monitoring, co-monitoring, and training visits.
  • Ensure that all study documentation and SOPS are maintained according to applicable regulations and industry-accepted standards, both in the field and in-house.
  • Contribute to the development of study documentation, including protocol review, study operations manuals, SOPs, ICFs, CRFs, CSRs, IBs, and data cleaning.
  • Collaborate with Clinical, Regulatory, and Quality team members to ensure compliance of department/study activities with FDA regulations, guidelines, and principles of ICH GCP and company SOPs.
  • Limited travel possible to clinical sites to supervise and/or monitor clinical studies (~25%).
Qualifications & Education
  • Bachelor’s or Master’s degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • 5 to 8 years of experience in clinical operations or direct study management in a biotech or pharmaceutical company (Industry Sponsor).
  • Excellent communication skills.
  • Extensive experience managing US clinical sites, including start-up activities and monitoring.
  • Experience in oncology (preferably in solid tumors); radiopharmaceuticals a plus.
  • Experience overseeing CROs and vendors, maintaining timelines, and overseeing budgets.
  • Experience with clinical data review and data management processes.
  • Excellent communication, organizational, and leadership skills.
  • Ability to work independently, plan, prioritize, and risk mediate in a fast-paced environment.
  • Strong working knowledge of GCP, ICH, and FDA regulations.
About Us
Channeling Energy. Changing Lives. ARTBIO redefines cancer care by discovering and developing a new class of Alpha Radioligand Therapies (ARTs), powered by unique Pb-212 isotope technology and seamless supply. Our team works tirelessly to bring therapies that matter to patients who need them.
 
The unique ARTBIO approach selects the optimal alpha-precursor isotope (212Pb) and tumor-specific targets to create therapeutics with the potential for the highest efficacy and safety. The company's AlphaDirect™ technology, a first-of-its-kind 212Pb isolation method, enables a distributed manufacturing approach for the reliable production and delivery of ARTs. ARTBIO is advancing multiple pipeline programs, with lead program AB001 currently in first-in-human trials. The company is shaped by a long-standing scientific legacy with nearly a century of pioneering work in radiation therapy conducted at the University of Oslo and Norway’s Radium Hospital.
 
Cancer is relentless. So are we. We are driven by a desire to do better for cancer patients, lowering the burden of toleration and safety while at the same time raising the bar on clinical efficacy and duration. As an emerging, global biotech with locations in Boston, Basel, London, and Oslo, we take advantage of diverse scientific depth and insights, which makes ARTBIO a unique place to work. 
 
 
EEO Statement
ARTBIO is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. If you have a disability or special need that requires accommodation, please let us know.
 
Questions and Application Process
If interested, please apply and send your CV to HR@artbio.com. All inquiries are treated confidentially.
 
ARTBIO does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between ARTBIO and the agency. ARTBIO will not pay any fees related to unsolicited resumes.