ZipRecruiter

Log In

1

Associate Director Of Clinical Research Jobs in Rochester, NY

ICON

Senior Clinical Research Associate

Rochester, NY · On-site

$110K - $138K/yr

Senior Clinical Research Associate- Northeast ICON is a global healthcare intelligence and clinical ... Providing training and guidance to site staff and other CRAs to maintain high standards of clinical ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

Socket.dev

Clinical Research Coordinator II

Rochester, NY · On-site

$55 - $81/hr

Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 years of clinical research or healthcare experience required * Experience in [gastroenterology ...

next page

Showing results 1-20

All JobsAssociate Of Clinical Research JobsAssociate Director Of Clinical Research JobsAssociate Director Of Clinical Research Jobs in Rochester, NY

Associate Director Of Clinical Research information

What does an associate director of clinical research do?

An Associate Director of Clinical Research oversees the planning, execution, and management of clinical trials and research studies within a healthcare or pharmaceutical organization. They ensure that studies comply with regulatory requirements, company policies, and ethical standards. This role involves managing teams, collaborating with various departments, and analyzing data to support new drug development or medical procedures. They also contribute to strategic decision-making and the improvement of clinical trial processes.

What are the key skills and qualifications needed to thrive as an associate director of clinical research?

To thrive as an Associate Director of Clinical Research, you need advanced knowledge of clinical trial design, regulatory compliance, and project management, usually supported by a degree in life sciences or a related field and significant clinical research experience. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and certifications such as CCRA or CCRP are typically expected. Leadership, strategic thinking, and strong interpersonal skills help drive cross-functional teams and effective stakeholder communication. These combined skills ensure trials are conducted efficiently, ethically, and in accordance with regulatory standards, which is critical for successful research outcomes.

How does an associate director of clinical research collaborate with cross-functional teams during a clinical trial?

An Associate Director of Clinical Research plays a central role in coordinating with various teams such as regulatory affairs, data management, biostatistics, and clinical operations. They ensure that study protocols are followed, timelines are met, and communication between departments is seamless. Regular meetings, progress updates, and collaborative problem-solving are key aspects of their daily routine. This cross-functional teamwork helps to address challenges efficiently and ensures that clinical trials run smoothly from start to finish.

What is the difference between Associate Director Of Clinical Research vs Clinical Project Manager?

AspectAssociate Director Of Clinical ResearchClinical Project Manager
CredentialsTypically requires a master's or doctoral degree in life sciences, along with experience in clinical research.Usually requires a bachelor's or master's degree in a related field, with relevant project management experience.
Work EnvironmentWorks in pharmaceutical or biotech companies, overseeing multiple clinical trials and teams.Manages specific clinical projects, coordinating activities between teams and vendors.
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and CROs, focusing on research oversight.Found in similar settings, focusing on project execution and timelines.

The Associate Director Of Clinical Research typically holds a higher-level role with broader oversight responsibilities compared to a Clinical Project Manager, who focuses on managing individual clinical projects. Both roles require relevant experience and credentials but differ mainly in scope and seniority.

What are popular job titles related to Associate Director Of Clinical Research jobs in Rochester, NY?

For Associate Director Of Clinical Research jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Associate Director Of Clinical Research jobs in Rochester, NY look for?

The top searched job categories for Associate Director Of Clinical Research jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Associate Director Of Clinical Research jobs?

Cities near Rochester, NY with the most Associate Director Of Clinical Research job openings:

Associate Director Of Clinical Research jobs near you
Infographic showing various Associate Director Of Clinical Research job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Clinical Research Associate

410 ICR United States USA

Rochester, NY • On-site

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 22 days ago

Job description

Senior Clinical Research Associate- Northeast

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply