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Medical Monitor Clinical Trial Jobs in Ridgefield, CT

Insight Global

Clinical Trial Support RN

New Haven, CT · On-site

$50 - $55/hr

  • Medical

  • Dental

  • Vision

  • Life

As a clinical trial support staff member, you will be responsible for coordinating and conducting ... You will also monitor and report on the safety and efficacy of the vaccine candidates, provide ...

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Medical Monitor Clinical Trial information

See Ridgefield, CT salary details

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

As of Aug 12, 2026, the average hourly pay for medical monitor clinical trial in Ridgefield, CT is $37.51, according to ZipRecruiter salary data. Most workers in this role earn between $25.62 and $47.88 per hour, depending on experience, location, and employer.

What is a medical monitor clinical trial?

A Medical Monitor in a clinical trial is a physician responsible for ensuring the safety of trial participants and the integrity of the study. They review and analyze clinical data, assess adverse events, and provide medical expertise to ensure compliance with regulatory and ethical guidelines. Medical Monitors collaborate with investigators, sponsors, and regulatory agencies to guide the trial's medical aspects. Their role is crucial in maintaining patient safety while ensuring the study's scientific and regulatory requirements are met.

What are the main daily responsibilities of a medical monitor in a clinical trial?

A Medical Monitor in a clinical trial is primarily responsible for overseeing participant safety and ensuring that the study is conducted in accordance with clinical protocols and regulatory standards. This involves reviewing and assessing adverse event reports, providing medical expertise to the clinical team, and communicating with investigators to resolve medical queries. You’ll also participate in safety data review meetings and contribute to key trial documents such as safety monitoring plans. The role requires ongoing collaboration with data management, regulatory, and pharmacovigilance teams to ensure a smooth and compliant trial process.

What are the key skills and qualifications needed to thrive in the medical monitor clinical trial position?

To thrive as a Medical Monitor Clinical Trial, you need an MD or equivalent medical degree, comprehensive clinical expertise, and experience with Good Clinical Practice (GCP) guidelines. Familiarity with clinical trial management systems, electronic data capture platforms, and relevant regulatory documentation is essential, as is certification such as Board Certification or GCP training. Strong analytical thinking, effective communication, and collaborative problem-solving skills make a candidate stand out in this role. These competencies are crucial to ensure participant safety, maintain regulatory compliance, and facilitate the success of clinical trials.

Medical Monitor Clinical Trial jobs near you
Infographic showing various Medical Monitor Clinical Trial job openings in Ridgefield, CT as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $78,029 per year, or $37.5 per hour.

Executive Medical Director, Neurology, Clinical Development (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 26 days ago

Job description

Contact: Alexandra Spink -
No 3rd party candidates

We are looking for an accomplished Executive Medical Director, Neurology Clinical Development to lead the strategy, execution, and oversight of global clinical development programs across neurology indications. This highly visible leadership role will drive clinical programs from early development through registration, provide medical leadership across cross-functional teams, and help shape the future of our neurology gene therapy portfolio.

As the medical lead for assigned programs, you will provide expert oversight of medical monitoring, clinical strategy, data interpretation, regulatory interactions, and scientific communications. Working collaboratively across Research, Clinical Operations, Regulatory Affairs, Biostatistics, Pharmacovigilance, Commercial, and other key stakeholders, you will play a critical role in advancing innovative therapies for patients with neurologic diseases.

Key Responsibilities

  • Lead the strategy, design, and execution of global clinical development programs across Phases I–III.
  • Serve as the therapeutic area lead for the Neurology Gene Therapy Clinical Development team, partnering with Clinical Operations, Toxicology, Regulatory Affairs, Commercial, Pharmacovigilance, Clinical Quality, and Biostatistics.
  • Provide medical oversight for clinical trials, ensuring patient safety, protocol compliance, data integrity, and study quality.
  • Lead clinical operational strategy, including site selection, enrollment, feasibility, and issue resolution.
  • Collaborate with Clinical Operations on medical monitoring, safety review, coding, and data cleaning.
  • Interpret clinical trial data and ensure the scientific integrity of study reports and communications.
  • Author or oversee clinical sections of regulatory submissions, including INDs, NDAs, BLAs, and briefing books.
  • Represent the company during regulatory agency interactions and Advisory Committee meetings.
  • Develop safety management documents, DMC charters, investigator communications, and other study-related materials.
  • Build relationships with CROs, investigators, key opinion leaders, consultants, and investigational sites.
  • Analyze and present clinical data through publications, presentations, scientific meetings, and advisory boards.
  • Maintain expertise in neurology and gene therapy through scientific literature and medical conferences.
  • Manage clinical development budgets, timelines, risks, and program progress.
  • Support business development, product evaluations, due diligence, and portfolio strategy.
  • Provide medical expertise to internal and external stakeholders across research, development, commercial, regulatory, manufacturing, and patient-focused functions.
  • Coach, mentor, and develop direct reports while fostering a collaborative, high-performing team.

Qualifications

  • MD (or foreign equivalent) with clinical training and experience in Neurology required.
  • PhD in a related scientific discipline preferred.
  • 10+ years of global clinical development experience in the pharmaceutical or biotechnology industry across Phases I–III.
  • 5+ years of leadership experience managing clinical development teams.
  • Pediatric neurology experience preferred.
  • Gene therapy experience preferred.
  • Strong expertise in medical monitoring, clinical trial design, regulatory strategy, and clinical data interpretation.
  • Thorough knowledge of ICH-GCP guidelines, FDA regulations, and global clinical development requirements.
  • Excellent leadership, communication, and cross-functional collaboration skills.
  • Ability to travel domestically and internationally up to 20%.