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Clinical Trials Director Jobs in Ridgefield, CT (NOW HIRING)

micro1 AI

Director of Biostatistics

Bridgeport, CT · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

New Haven, CT · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Stamford, CT · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

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Clinical Trials Director information

See Ridgefield, CT salary details

$10

$54

$116

How much do clinical trials director jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical trials director in Ridgefield, CT is $54.11, according to ZipRecruiter salary data. Most workers in this role earn between $32.31 and $71.35 per hour, depending on experience, location, and employer.

What is the difference between Clinical Trials Director vs Clinical Research Manager?

AspectClinical Trials DirectorClinical Research Manager
ResponsibilitiesOversees entire clinical trial programs, manages teams, and ensures regulatory complianceManages daily operations of clinical research projects, coordinates activities, and supports trial execution
Required CredentialsTypically requires a clinical research or life sciences degree, with extensive experienceRequires similar degrees and experience, often with less strategic oversight
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple projectsOperational roles within research sites or CROs, focusing on project execution

The Clinical Trials Director focuses on strategic oversight and leadership of clinical trial programs, while the Clinical Research Manager handles day-to-day project management. Both roles require relevant credentials and industry experience, but differ in scope and level of responsibility.

What are some common challenges faced by a clinical trials director and how can they be managed?

Clinical Trials Directors often encounter challenges such as coordinating large, cross-functional teams, ensuring strict regulatory compliance, and managing tight timelines for multiple studies. Effective communication, strong leadership, and proactive risk management are essential to address these issues. Staying updated on regulatory changes and fostering collaboration between departments can also help streamline processes and ensure trials run efficiently.

What does a clinical trials director do?

A Clinical Trials Director oversees the planning, execution, and management of clinical research trials to ensure they are conducted ethically, safely, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and ensure that trials meet scientific and operational objectives. Their responsibilities also include liaising with regulatory agencies, monitoring trial progress, and addressing any issues that arise during the study.

What are the key skills and qualifications needed to thrive as a clinical trials director?

To thrive as a Clinical Trials Director, you need a strong background in clinical research, regulatory compliance, and project management, typically supported by an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are commonly required. Exceptional leadership, strategic thinking, and communication skills are crucial for managing cross-functional teams and stakeholder relationships. These competencies ensure successful trial execution, regulatory adherence, and the delivery of safe and effective clinical outcomes.

What cities near Ridgefield, CT are hiring for Clinical Trials Director jobs?

Cities near Ridgefield, CT with the most Clinical Trials Director job openings:

Clinical Trials Director jobs near you
Infographic showing various Clinical Trials Director job openings in Ridgefield, CT as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,551 per year, or $54.1 per hour.

Associate Medical Director, Clinical Development, Ophthalmology

PVH (Tommy Hilfiger/Calvin Klein)

Tarrytown, NY • On-site

$243.60 - $329.40/hr

Other

Posted 11 days ago

PVH Corp. rating

6.3

Company rating: 6.3 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

Job description

Associate Medical Director, Clinical Development, Ophthalmology

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Clinical Development Program (CDP) team, supporting our Ophthalmology therapeutics portfolio. In this role, you will serve as Medical Lead for clinical trials, designing clinical study concepts and leading the Global Clinical Study Team, while collaborating with discovery teams, the Therapeutic Head, and Strategic Program Teams to deliver high-quality, scientifically sound program milestones. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Location: Tarrytown, NY or Cambridge, MA
Travel: 10% to relevant conferences

Discover your role:
  • Act as medical expert and leader in interactions with external stakeholders
  • Define clinical trial-related Clinical Development Program goals and objectives
  • Partner with discovery teams to shape the next generation of targets in the field
  • Ensure the scientific accuracy of clinical study concepts through rigorous review and consultation with internal and external experts
  • Present clinical study concepts to the Therapeutic Head, Strategic Program Teams, and internal governance meetings
  • Lead the Global Clinical Study Team to deliver high-quality program milestones on schedule
  • Oversee the medical content of clinical study reports and the analysis of clinical data, including safety monitoring, to ensure patient safety
This role requires:
  • MD or equivalent, with board eligibility or certification in Ophthalmology
  • 0-2 years of academic clinical or translational research experience
  • Experience in Ophthalmic drug development strongly preferred

#MDJobs, #MDJobsCD, #Ophthalmology, #GDTherapeuticJobs

Does this sound like you?

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. For more information about on-site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$243,600.00 - $329,400.00

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