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Contract Senior Clinical Research Associate Jobs

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a ... This will be for a 6 month contract. As a Clinical Research Associate at ICON , you will play a ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal ...

Icon plc

Senior Clinical Research Associate

Chicago, IL · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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Contract Senior Clinical Research Associate information

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$36K

$94.3K

$143.5K

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

As of Aug 8, 2026, the average yearly pay for contract senior clinical research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What is a contract senior clinical research associate?

A Contract Senior Clinical Research Associate (CRA) is an experienced clinical research professional who works independently or through an agency on a contract basis, rather than as a permanent employee. Their primary role is to monitor clinical trials, ensuring that studies are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Senior CRAs have advanced knowledge of clinical trial processes and often oversee multiple sites or junior staff. They are responsible for reviewing data, managing documentation, and acting as a liaison between the study sponsor and the investigative sites. Contract positions offer flexibility and variety, but may require more travel and self-management.

What skills and qualifications are needed to thrive as a contract senior clinical research associate?

To thrive as a Contract Senior Clinical Research Associate, you need comprehensive knowledge of clinical trial processes, GCP/ICH guidelines, and relevant regulatory requirements, typically supported by a life sciences degree and several years of monitoring experience. Familiarity with Electronic Data Capture (EDC) systems, trial management software, and certifications like ACRP or SOCRA are commonly required. Exceptional organizational skills, attention to detail, and effective communication make someone stand out in this role. These skills and qualities are vital to ensure protocol compliance, high data quality, and successful collaboration across study sites.

How does a contract senior clinical research associate typically collaborate with study sites and sponsors during a clinical trial?

As a Contract Senior Clinical Research Associate (CRA), you play a key liaison role between study sites and sponsors. You are responsible for monitoring site performance, ensuring protocol compliance, and addressing any issues that arise during the trial. Regular communication with site staff and sponsor representatives is essential, often involving site visits, remote monitoring, and reporting. Effective collaboration helps maintain study integrity, ensures regulatory requirements are met, and facilitates the timely progression of the clinical trial.

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

AspectContract Senior Clinical Research AssociateClinical Research Associate
CredentialsBachelor's degree, relevant certifications, experience in clinical trialsBachelor's degree, entry-level certifications often sufficient
Work EnvironmentContract basis, often in multiple sites or projects, possibly remoteFull-time or part-time, typically at a single site or sponsor location
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms, project-basedPharmaceutical companies, CROs, hospitals, research sites

The Contract Senior Clinical Research Associate typically has more experience, handles complex trial aspects, and works on a contractual basis. The Clinical Research Associate is often an entry-level or mid-level role focused on site monitoring and data collection. Both roles are essential in clinical trials but differ mainly in experience level and employment type.

More about Contract Senior Clinical Research Associate jobs
What cities are hiring for Contract Senior Clinical Research Associate jobs? Cities with the most Contract Senior Clinical Research Associate job openings:
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What job categories do people searching Contract Senior Clinical Research Associate jobs look for? The top searched job categories for Contract Senior Clinical Research Associate jobs are:
Contract Senior Clinical Research Associate jobs near you
Infographic showing various Contract Senior Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Senior Clinical Research Associate

410 ICR United States USA

Blue Bell, PA • Remote

Full-time

Posted 22 days ago

Job description

Senior CRA

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.


We are currently seeking a Contractor Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month contract. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

  • Bachelor’s degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • Minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

#LI-Remote #LI-ZH1


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.

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