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Clinical Trials Director Jobs in Rochester, NY (NOW HIRING)

Director of Biostatistics

Rochester, NY ยท 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 ...

Director, Thoracic Surgery

Pavilion, NY ยท On-site

$550K - $600K/yr

The Director will collaborate with an outstanding team of pulmonologists, medical and radiation ... Valley has a robust clinical trials infrastructure, and ongoing clinical trials for patients with ...

Director, Thoracic Surgery

Pavilion, NY ยท On-site

$550K - $600K/yr

The Director will collaborate with an outstanding team of pulmonologists, medical and radiation ... Valley has a robust clinical trials infrastructure, and ongoing clinical trials for patients with ...

Director, Thoracic Surgery

Pavilion, NY ยท On-site

$550K - $600K/yr

The Director will collaborate with an outstanding team of pulmonologists, medical and radiation ... Valley has a robust clinical trials infrastructure, and ongoing clinical trials for patients with ...

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Clinical Trials Director information

See Rochester, NY salary details

$10

$53

$115

How much do clinical trials director jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical trials director in Rochester, NY is $53.61, according to ZipRecruiter salary data. Most workers in this role earn between $32.02 and $70.67 per hour, depending on experience, location, and employer.

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 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 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 the most commonly searched types of Clinical Trials jobs in Rochester, NY?

The most popular types of Clinical Trials jobs in Rochester, NY are:

What are popular job titles related to Clinical Trials Director jobs in Rochester, NY?

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

What cities near Rochester, NY are hiring for Clinical Trials Director jobs?

Cities near Rochester, NY with the most Clinical Trials Director job openings:

Infographic showing various Clinical Trials Director job openings in Rochester, NY as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 20% Part Time, and 6% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $111,503 per year, or $53.6 per hour.

Clinical Trials Registered Nurse, Oncology Research Clinical Trials, Full Time, Day

Valley Health System

Pavilion, NY โ€ข On-site

$45.52 - $56.90/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago


Job description

**SIGN ON BONUS**
POSITION SUMMARY:
To coordinate and implement clinical research protocols under the direction of the Director of Oncology Clinical Trials and Research Compliance, provide care to all or some of the patient's enrolled in each protocol, act as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the protocol, and coordinate all nursing activities specifically related to the implementation of the treatment regimen.
SCHEDULE:
This position is onsite and part of the Valley Clinical Trials Research Program, focusing on Oncology. It is a full-time, day shift role, Monday through Friday, with hours from 8:00 AM to 4:30 PM or 8:30 AM to 5:00 PM, totaling 40 hours per week or 80 hours bi-weekly.
In this role, your day typically includes:
- Screening and enrolling patients
- Obtaining informed consent
- Providing ongoing education and support to participants
- Coordinating study visits and performing protocol-specific procedures
- Ensuring accurate documentation of all research activities
You will collaborate closely with investigators, coordinators, and multidisciplinary teams to maintain protocol adherence, patient safety, and data integrity.
EDUCATION:
Bachelor`s degree in Nursing required. Current/valid State of New Jersey license (or legal permission to work from the New Jersey Board of Nursing.
EXPERIENCE:
2-5 years of RN experience with Clinical Research Background. Computer and keyboard skills. Medical terminology required.
SPECIAL SKILLS:
Physical and cognitive requirements: Position's physical requirements necessitate a full range of body motion including but not limited to, physically assisting patients, requiring stretching, bending, lifting, sitting, kneeling, stooping, standing, walking, pushing and pulling. Position is classified according to the USDOL as Very Heavy Work which is defined as exerting in excess of 100 pounds of force occasionally, and/or in excess of 50 pounds of force frequently, and/or in excess of 20 pounds of force constantly to move objects. The National Institute of Safety and Health (NIOSH0 guidelines, which recommends that the average worker not lift more than 51 pounds without assistance, will be followed. Manual and finger dexterity and hand-eye coordination are also required as is constant talking and listening in English. Must demonstrate effective oral and written communication skills, including speech clarity, understanding the information relayed, deductive and inductive reasoning skills (the ability to apply general rules to specific problems to produce answers that make sense and the ability to combine pieces of information to/from general rules or conclusion respectively). Considerable walking, standing, sitting, reaching, filing, typing and photocopying required. Ability to perform work accurately and pay attention to details, often changing from one task to another without loss of efficiency or composure. Ability to function competently in stressful situations and changing work environment related to changing needs of patients with acute, chronic and complex and/or terminal disease processes. Ability to work cooperatively within health system, multidisciplinary team members (i.e. MD's, Rehab, Respiratory, DI, Laboratory, etc). Ability to utilize effective time management skills to set priorities to perform responsibilities, problem solve and deliver care. IV certification.
Job Location
Luckow Pavilion
Shift
Day (United States of America)
Benefits
  • Medical/Prescription, Dental & Vision Discount Program (Full Time/Part Time Employees)
  • Group Term Life Insurance and AD&D(Full Time Employees)
  • Flexible Spending Accounts and Commuter Benefit Plans
  • Supplemental Voluntary Benefits ( e.g. Short-term and Long-term Disability, Whole Life Insurance, Legal Support, etc.)
  • 6 Paid Holidays, Paid Time Off (varies), Wellness Time Off, Extended Illness
  • Retirement Plan
  • Tuition Assistance
  • Employee Assistance Program (EAP)
  • Valley Health LifeStyles Fitness Center Membership Discount
  • Day Care Discounts for Various Daycare Facilities

Salary
Joining Valley Health System means becoming part of a dedicated team that values the highest quality of care in a supportive environment. In our commitment to high performance and reliability, we encourage and recognize exceptional individual performance through our industry leading compensation practices including a starting salary and benefits in accordance with your role, experience, education, and licensure. Actual individual salaries vary depending on these factors. The salary listed does not include other forms of compensation or benefits.
Pay Range: $45.52 - $56.90 (per hour)
EEO Statement
Valley Health System does not discriminate on the basis of ancestry, age, atypical hereditary cellular or blood trait, civil union status, color, creed, disability, domestic partnership, gender, gender identity or expression, familial status, genetic information, liability for service in the Armed Forces of the United States, marital status, medical condition or illness, mental or physical handicap, national origin, nationality, perceived disability, pregnancy, race, refusal to submit to genetic testing or make available results of such tests, religion, sex, sexual orientation, veteran's status or any other protected basis, in accordance with all applicable Federal, State and Local laws. This applies to all areas of employment, including recruitment, hiring, training and development, promotion, transfer, termination, layoff, compensation, benefits, social and recreational programs, and all other conditions and privileges of employment.