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Remote Medical Monitor Jobs in Boston, MA (NOW HIRING)

Sr. Tax Manager (REMOTE)

Waltham, MA · Remote

$134K - $167K/yr

Collaborate with finance, legal, and operations teams to implement and monitor tax strategies ... Medical, Dental, and Vision Insurance Options * Life and Disability Insurance * Paid Time-Off

Sr. Tax Manager (REMOTE)

Waltham, MA · Remote

$134K - $167K/yr

Collaborate with finance, legal, and operations teams to implement and monitor tax strategies ... Medical, Dental, and Vision Insurance Options * Life and Disability Insurance * Paid Time-Off

Showing results 21-40

Remote Medical Monitor information

See Boston, MA salary details

$22.8K

$100.6K

$193.4K

How much do remote medical monitor jobs pay per year?

As of Sep 2, 2026, the average yearly pay for remote medical monitor in Boston, MA is $100,552.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,800.00 and $91,800.00 per year, depending on experience, location, and employer.

What is a remote medical monitor?

A Remote Medical Monitor is a healthcare professional, typically a physician, who oversees the safety and efficacy of clinical trials from a remote location. They are responsible for reviewing patient data, monitoring adverse events, and ensuring compliance with study protocols without being physically present at the trial site. Remote Medical Monitors play a crucial role in maintaining the integrity of clinical research, facilitating timely decisions, and ensuring patient safety. Their work allows for greater flexibility and efficiency in clinical trial management, especially in multi-site or decentralized studies.

What are the key skills and qualifications needed to thrive as a remote medical monitor?

To thrive as a Remote Medical Monitor, you need a medical degree (MD or equivalent), clinical experience, and a strong understanding of clinical trial protocols and regulations. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification are typically required. Excellent analytical skills, attention to detail, and effective remote communication are vital soft skills for this role. These abilities ensure accurate oversight of patient safety and data integrity in decentralized clinical trials.

How does a remote medical monitor effectively collaborate with clinical trial teams across different time zones?

As a Remote Medical Monitor, you will regularly coordinate with clinical research associates, investigators, and data management teams who may be located globally. Effective collaboration often involves flexible scheduling for virtual meetings, clear written communication, and proactive updates to ensure all team members are aligned. Utilizing project management tools and maintaining detailed documentation helps streamline workflows and reduce misunderstandings. Strong organizational skills are essential to manage time zone differences and ensure timely responses to safety queries or protocol deviations.

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

AspectRemote Medical MonitorRemote Clinical Research Associate
Required CredentialsMedical degree or clinical background, certifications like CCRP or CCRA often preferredDegree in life sciences, healthcare, or related field; certifications like CCRP common
Work EnvironmentRemote, primarily reviewing clinical trial data and safety reportsRemote or onsite, overseeing trial sites and monitoring compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, research institutions

While both roles support clinical trials remotely, Remote Medical Monitors focus on safety data review and medical oversight, whereas Remote Clinical Research Associates primarily oversee trial site activities and compliance. Both require healthcare or scientific backgrounds and are common in the pharmaceutical and biotech industries.

What are the most commonly searched types of Medical Monitor jobs in Boston, MA?

The most popular types of Medical Monitor jobs in Boston, MA are:

What cities near Boston, MA are hiring for Remote Medical Monitor jobs?

Cities near Boston, MA with the most Remote Medical Monitor job openings:

Head of Clinical Affairs - medical device dental implant start-up (REMOTE)

InnoTech Staffing

Cambridge, MA • Remote

$81K - $111K/yr

Full-time

Medical, Dental, Retirement, PTO

Re-posted 21 days ago


Job description

InnoTECH Staffing has partnered with an exciting medical device start-up and is looking to hire a fulltime permanent Head of Clinical Affairs.   This is a REMOTE position. 

Ideal candidate will have experience leading clinical strategy for Class II implant start-up, along with 10+ years of clinical study execution & submission experience in the medical device industry. Lastly, should have demonstrated experience leading FDA IDE pivotal clinical studies through execution.

There is no sponsorship offered - must be a US Citizen or GreenCard holder.

  About the Role

We are seeking an experienced and hands-on Head of Clinical Affairs to lead clinical strategy, starting with the execution of our pivotal study. This individual will serve as the clinical leader for the program, providing both strategic oversight and day-to-day operational guidance to ensure successful study execution.

Key Responsibilities Clinical Strategy & Leadership

●     Lead the overall clinical strategy, ensuring alignment with regulatory and business objectives.

●     Develop and execute strategies for site selection, enrollment, risk management and data quality.

●     Manage partners and process to facilitate shipment of clinical study products from the US to a clinical site in Sao Paulo, Brazil.

●     Serve as the primary clinical subject matter expert for executive leadership, the Board of Directors, investors, and external stakeholders.

●     Collaborate closely with company team members to support FDA interactions, including pre-submissions, IDE submissions and responses to agency feedback.

Clinical Study Readiness & Execution Plan

●     Develop and execute a plan to demonstrate the Company’s enrollment targets are achievable within the timeframe budgeted for in the operating plan.

●     Manage preparation of clinical study infrastructure, operational controls, and vendor (CRO, EDC, TMF) selection and management.

●     Lead process for clinical site readiness, including finalizing site budgets, contracts, IRB approvals, site qualifications and site initiation visits.

●     Partner with clinical sites to develop a robust site specific patient recruitment plan to achieve their enrollment targets.

●     Identify operational risks and implement mitigation plans to ensure study success.

Clinical Operations Oversight

●     Oversee the execution of the IDE clinical study, ensuring milestones, timelines, enrollment targets, and budgets are achieved.

●     Monitor study progress, enrollment, data quality, protocol compliance, site performance, and patient retention.

●     Ensure that clinical investigation strictly adheres to GCP guidelines and ISO 14155.

●     Partner with investigators and clinical sites to support successful study conduct and participant recruitment.

●     Assist with preparation of clinical materials for regulatory submissions, investor presentations, scientific publications, and conference presentations.

Qualifications Required

●     10+ years of clinical study execution & submission experience in the medical device industry.

●     Demonstrated experience leading FDA IDE pivotal clinical studies through execution.

●     Deep understanding of FDA regulations governing medical device clinical trials, including IDE requirements, Good Clinical Practice (GCP), and ISO 14155.

●     Experience managing CROs and external clinical vendors.

●     Strong knowledge of clinical study design, execution, monitoring and data management.

●     Excellent leadership, communication, and stakeholder management skills.

●     Ability to operate effectively in a fast-paced startup environment with limited resources.

●     Experience implementing clinical SOPs.

Personal Attributes

●     Strategic thinker who is also willing to engage in day-to-day operational execution.

●     Highly organized with strong project management capabilities.

●     Collaborative and team-oriented leadership style.

●     Comfortable navigating ambiguity and helping build processes from the ground up.

●     Strong sense of accountability and ownership.

Compensation

●     Competitive salary, benefits and equity commensurate with experience.

Regarding benefits, the company currently offers cash reimbursement for health and dental insurance premiums. 

They are a small team (only two full-time employees), so they have not initiated a group health plan yet, though they plan to as the team grows. They do not currently offer a 401K match. Again, they plan to offer this as the team grows. They offer unlimited vacation and fully remote work.