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Associate Merck Clinical Trials Jobs in Rochester, NY

Registered Nurse

Rochester, NY · On-site

$38.67 - $51.92/hr

... treatments , clinical trials, and multidisciplinary care from experts in medical and radiation ... REQUIRED QUALIFICATIONS: · Diploma or Associate's Degree in Nursing · Registered Nurse license in ...

Registered Nurse

Rochester, NY · On-site

$38.67/hr

... treatments , clinical trials, and multidisciplinary care from experts in medical and radiation ... REQUIRED QUALIFICATIONS: · Diploma or Associate's Degree in Nursing · Registered Nurse license in ...

Registered Nurse

Rochester, NY · On-site

$38.67 - $51.92/hr

... treatments , clinical trials, and multidisciplinary care from experts in medical and radiation ... REQUIRED QUALIFICATIONS: · Diploma or Associate's Degree in Nursing · Registered Nurse license in ...

Registered Nurse

Rochester, NY · On-site

$38.67 - $51.92/hr

... treatments , clinical trials, and multidisciplinary care from experts in medical and radiation ... REQUIRED QUALIFICATIONS: · Diploma or Associate's Degree in Nursing · Registered Nurse license in ...

The Clinical Specialist/Optometric Assistant is primarily responsible for helping ensure a great ... In partnership with the retail associates, schedule appointments and manage exam books according to ...

Optometric Assistant

Webster, NY · On-site

$17 - $25.50/hr

The Clinical Specialist/Optometric Assistant is primarily responsible for helping ensure a great ... In partnership with the retail associates, schedule appointments and manage exam books according to ...

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Showing results 1-20

Associate Merck Clinical Trials information

See Rochester, NY salary details

$17

$39

$69

How much do associate merck clinical trials jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for associate merck clinical trials in Rochester, NY is $39.45, according to ZipRecruiter salary data. Most workers in this role earn between $31.78 and $43.41 per hour, depending on experience, location, and employer.

What is the difference between Associate Merck Clinical Trials vs Clinical Research Coordinator?

AspectAssociate Merck Clinical TrialsClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications (e.g., CCRP)Bachelor's degree, often similar certifications
Work EnvironmentPharmaceutical company, clinical trial sites, research labsHospital, research sites, clinics
Employer & IndustryPharmaceutical industry, biotech firmsHealthcare facilities, research organizations
Common Search & ComparisonYesYes

The Associate Merck Clinical Trials role typically involves supporting clinical trial activities within a pharmaceutical company, focusing on drug development and regulatory compliance. In contrast, a Clinical Research Coordinator manages patient recruitment, data collection, and trial logistics at research sites. Both roles require similar educational backgrounds and certifications, but their work environments and specific responsibilities differ, with the Associate Merck Clinical Trials position being more industry-focused and the Clinical Research Coordinator more patient-facing.

What are the most commonly searched types of Merck Clinical Trials jobs in Rochester, NY? The most popular types of Merck Clinical Trials jobs in Rochester, NY are:
What are popular job titles related to Associate Merck Clinical Trials jobs in Rochester, NY? For Associate Merck Clinical Trials jobs in Rochester, NY, the most frequently searched job titles are:
What cities near Rochester, NY are hiring for Associate Merck Clinical Trials jobs? Cities near Rochester, NY with the most Associate Merck Clinical Trials job openings:
Infographic showing various Associate Merck Clinical Trials job openings in Rochester, NY as of July 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $82,061 per year, or $39.5 per hour.

Senior Clinical Research Associate

410 ICR United States USA

Rochester, NY • Hybrid

$110K - $138K/yr

Full-time

Posted 10 days ago


Job description

Senior Clinical Research Associate - Oncology - New York

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.


Responsibilities: 

  • Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness 

  • Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites 

  • Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials 

  • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs 

  • Promptly document monitoring activities and submit/approve visit reports  

  • Manage site essential document collection and TMF reconciliation with site files 

  • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals 

  • Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution 

  • Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans 

  • Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations 

  • Support sites and the client's regulatory inspections 

  • Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities  

  • Lead site engagement initiatives and foster relationships with key Oncology sites and networks  

Qualifications 

  • Bachelor’s degree (scientific field preferred) 

  • 5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.

  • 1+ years early development trial experience  

  • Solid tumor clinical trial experience is required

  • Experience utilizing Veeva systems is highly preferred 

  • Demonstrated experience developing/maintaining site relationships and securing compliance 

  • Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology 

  • Experience collaborating with sites from initial engagement through close-out phases 

  • Experience activating sites 

  • Experience training site staff 

  • Experience supporting sites and/or sponsors in regulatory inspections 

  • Experience working within a Functional Services (or in-house) monitoring model is preferred 

  • Willing to travel up to 50% 


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