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Virtual Senior Clinical Research Associate Jobs in Rochester, NY

Senior CRA

Rochester, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NJ/NY ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Senior CRA

Rochester, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NY/NJ ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Senior CRA

Rochester, NY · On-site +1

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Senior CRA

Rochester, NY · On-site +1

$110K - $138K/yr

Senior CRA- Phase I Oncology/NY/NJ ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Senior CRA

Rochester, NY

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

... and senior research staff. * Conduct screening visits to collect medical history & other ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

... and senior research staff. * Conduct screening visits to collect medical history & other ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

... and senior research staff. * Conduct screening visits to collect medical history & other ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

... and senior research staff. * Conduct screening visits to collect medical history & other ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

Senior CRA- Phase I Oncology/NJ/NY ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Research Associate

Rochester, NY · On-site

$20.75 - $27.75/hr

Various Clinical Sites Hours Per Week: 40 hours per week Schedule: Full-time, Day Shift, Monday to Friday, 8 am- 4.30 pm. Position Summary: The Research Associate will be tasked with conducting work ...

Research Associate

Batavia, NY · On-site

$69K - $92K/yr

... Research Associate, Quantum Division conducts research related to the overall mission of the ... virtual interview. Equal Opportunity Statement Fermilab is an equal opportunity employer. We ...

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Showing results 1-20

Virtual Senior Clinical Research Associate information

See Rochester, NY salary details

$35.5K

$93.1K

$141.6K

How much do virtual senior clinical research associate jobs pay per year?

As of Aug 10, 2026, the average yearly pay for virtual senior clinical research associate in Rochester, NY is $93,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,700.00 and $126,300.00 per year, depending on experience, location, and employer.

What is the difference between Virtual Senior Clinical Research Associate vs Virtual Clinical Research Associate?

AspectVirtual Senior Clinical Research AssociateVirtual Clinical Research Associate
Required CredentialsTypically requires 3+ years of experience, relevant certifications (e.g., CCRP), and advanced knowledge of clinical trialsEntry to mid-level experience, often with similar certifications but less experience required
Work EnvironmentRemote, overseeing multiple sites, managing complex trial phasesRemote or hybrid, supporting trial activities under supervision
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSimilar employers, often as entry-level or supporting roles

The Virtual Senior Clinical Research Associate typically has more experience and handles complex trial oversight, while the Virtual Clinical Research Associate is often an entry or mid-level role supporting clinical trial activities remotely.

What are popular job titles related to Virtual Senior Clinical Research Associate jobs in Rochester, NY? For Virtual Senior Clinical Research Associate jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Virtual Senior Clinical Research Associate jobs in Rochester, NY look for? The top searched job categories for Virtual Senior Clinical Research Associate jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Virtual Senior Clinical Research Associate jobs? Cities near Rochester, NY with the most Virtual Senior Clinical Research Associate job openings:
Infographic showing various Virtual Senior Clinical Research Associate job openings in Rochester, NY as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $93,057 per year, or $44.7 per hour.

Senior Clinical Research Associate

410 ICR United States USA

Rochester, NY • Hybrid

$110K - $138K/yr

Full-time

Posted 25 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