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Senior Cra Jobs in Rochester, NY (NOW HIRING)

NBT Bank

Affordable Housing Originator

Fairport, NY

Complete understanding of CRA & Banking Regulations. * Working knowledge of workflow application ... Career Development Whether you're just starting your career or serve in a senior leadership role ...

NBT Bank

Affordable Housing Originator

Fairport, NY · On-site

Complete understanding of CRA & Banking Regulations. * Working knowledge of workflow application ... Career Development Whether you're just starting your career or serve in a senior leadership role ...

NBT Bank

Senior Relationship Banker

Webster, NY · On-site

$20.10 - $26.79/hr

Pay Range: $20.10 - $26.79 The role of the Senior Relationship Banker is to provide quality ... Reinvestment Act CRA. * 10% Performs other duties as assigned including but not limited to ...

NBT Bank

Senior Relationship Banker

Webster, NY

$20.10 - $26.79/hr

Pay Range: $20.10 - $26.79 The role of the Senior Relationship Banker is to provide quality ... Reinvestment Act CRA. * 10% Performs other duties as assigned including but not limited to ...

Five Star Bank

Chief Compliance Officer

Rochester, NY · On-site

$160K - $210K/yr

As a key senior leader of a growing and innovative financial institution, the Chief Compliance ... CRA) programs, to ensure compliance with applicable laws and regulations while proactively ...

NBT Bank

Relationship Banking Associate

Fairport, NY · On-site

$18.50 - $20.81/hr

... CRA. * 5% Performs other duties as assigned and required. Physical Requirements: * Communicate ... Career Development Whether you're just starting your career or serve in a senior leadership role ...

All JobsCra JobsSenior Cra JobsSenior Cra Jobs in Rochester, NY

Senior Cra information

See Rochester, NY salary details

$35.5K

$93.1K

$141.6K

How much do senior cra jobs pay per year?

As of Jul 26, 2026, the average yearly pay for senior cra 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.

How does a Senior Clinical Research Associate (CRA) typically collaborate with site staff and project teams during a clinical trial?

A Senior CRA regularly works with site staff, including investigators and coordinators, to ensure clinical trials are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines. They serve as a key liaison, communicating study updates, addressing site concerns, and providing training when needed. Additionally, Senior CRAs often collaborate with project managers, data managers, and other CRAs to monitor progress, resolve issues, and ensure data integrity. This teamwork is critical for maintaining study timelines and overall trial quality.

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

AspectSenior CraClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trials, often some certificationsBachelor's degree, entry-level to mid-level experience, some certifications
Work EnvironmentLeads monitoring activities, manages sites, mentors junior staffPerforms site monitoring, data collection, and compliance checks
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

The main difference between a Senior Cra and a Clinical Research Associate is experience level and responsibilities. Senior Cras typically oversee monitoring activities, mentor junior staff, and handle more complex tasks, while Clinical Research Associates focus on site monitoring and data collection. Both roles are essential in clinical trials and share similar industry environments and credentials.

What jobs can I get after being a CRA?

After working as a Clinical Research Associate (CRA), you can transition into roles such as Clinical Project Manager, Clinical Operations Manager, Regulatory Affairs Specialist, or Medical Writer. These positions often require experience in clinical trial management, regulatory knowledge, and strong communication skills, and may involve overseeing study progress, ensuring compliance, or coordinating between teams.

What are the key skills and qualifications needed to thrive as a Senior Clinical Research Associate (CRA), and why are they important?

To thrive as a Senior Clinical Research Associate, you need deep knowledge of clinical trial protocols, regulatory guidelines (such as GCP), and several years of hands-on experience in clinical monitoring. Familiarity with electronic data capture (EDC) systems, CTMS platforms, and certifications like ACRP or SOCRA are commonly required. Excellent organizational skills, attention to detail, and effective communication are soft skills that set top candidates apart. These skills ensure trial integrity, regulatory compliance, and smooth collaboration among sponsors, sites, and teams.

What does a senior CRA do?

A senior Clinical Research Associate (CRA) oversees and monitors clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They coordinate site activities, review data quality, and may mentor junior staff, often using monitoring tools and working closely with investigators and sponsors. Strong organizational skills and knowledge of clinical trial processes are essential for this role.

How much does a senior CRA make at Thermo Fisher?

A Senior Clinical Research Associate (CRA) at Thermo Fisher typically earns between $80,000 and $110,000 annually, depending on experience, location, and certifications. The role involves monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What are Senior CRAs?

Senior Clinical Research Associates (Senior CRAs) are experienced professionals responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory guidelines, protocols, and good clinical practice. They play a key role in managing study sites, reviewing data, and ensuring the integrity and quality of clinical research. Senior CRAs also mentor junior staff, resolve complex issues, and maintain effective communication between sponsors, sites, and regulatory bodies. Their expertise helps ensure that clinical trials are conducted safely and efficiently.

What is the average salary of a CRA in the US?

The average salary of a Clinical Research Associate (CRA) in the US is approximately $70,000 to $90,000 per year, depending on experience, location, and certifications. Senior CRAs with extensive experience can earn over $100,000 annually, often with additional benefits and bonuses.
What are the most commonly searched types of Cra jobs in Rochester, NY? The most popular types of Cra jobs in Rochester, NY are:
What are popular job titles related to Senior Cra jobs in Rochester, NY? For Senior Cra jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Senior Cra jobs in Rochester, NY look for? The top searched job categories for Senior Cra jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Senior Cra jobs? Cities near Rochester, NY with the most Senior Cra job openings:
Senior Cra jobs near you
Infographic showing various Senior Cra job openings in Rochester, NY as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $93,057 per year, or $44.7 per hour.

Senior CRA- Phase I Oncology- NJ/NY

410 ICR United States USA

Rochester, NY

$110K - $138K/yr

Full-time

Posted 2 days ago

Job description

Senior CRA- Phase I Oncology/NY/NJ

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