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

Doist

Senior Director, Clinical Science

Stamford, CT · On-site

$266 - $344/hr

The Senior Director, Clinical Science provides senior scientific and strategic leadership for the design, execution, and interpretation of clinical trials across one or more therapeutic programs.

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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.

Senior Medical Director, Clinical Development, Endocrinology

Regeneron Pharmaceuticals, Inc

Tarrytown, NY • On-site

$333.30 - $450.90/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago

Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Senior Medical Director, Clinical Development, Endocrinology

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 Senior Medical Director to join our Endocrinology team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross‑functional stakeholders. This role requires a high‑performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.

This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

When & where:
  • Work Location: Tarrytown, NY, Washington D.C., or Cambridge, Massachusetts
  • Travel: 10% to relevant conferences
Discover your role:
  • You guide the Global Clinical Study Team to deliver high‑quality trials on time.
  • You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance.
  • You lead clinical study and protocol development and present to internal and external stakeholders.
  • You provide clinical and scientific leadership for data review, study reports, and publications.
  • You work closely with cross‑functional partners to advance program goals and key deliverables.
  • You collaborate with discovery teams to help shape future targets and development opportunities in the field.
This role requires:
  • An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.
  • At least 4 years of pharmaceutical industry experience in clinical development (equivalent research in academia will be considered).
  • Experience in rare disease drug development strongly preferred.
  • Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage.

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.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.

Salary Range (annually)

$333,300.00 - $450,900.00

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