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Associate International Clinical Research Jobs (NOW HIRING)

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...

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Associate International Clinical Research information

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$36K

$94.3K

$143.5K

How much do associate international clinical research jobs pay per year?

As of Aug 8, 2026, the average yearly pay for associate international clinical research 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 the difference between Associate International Clinical Research vs Clinical Research Coordinator?

AspectAssociate International Clinical ResearchClinical Research Coordinator
Required CredentialsBachelor's degree, often in life sciences; certifications like CCRP or GCP trainingBachelor's degree, relevant certifications often preferred
Work EnvironmentGlobal or multi-site clinical trials, often in international settingsSingle-site or multi-site clinical trial management, primarily in hospitals or research centers
Employer & Industry UsagePharmaceutical companies, CROs, academic institutions involved in international studiesHospitals, research institutions, pharmaceutical companies conducting clinical trials
Common Search & ComparisonYesYes

While both roles support clinical trial processes, the Associate International Clinical Research typically focuses on international or multi-site studies, requiring global coordination skills. The Clinical Research Coordinator usually manages local or site-specific trials, emphasizing patient interaction and trial administration. Understanding these differences helps candidates choose the role that best fits their experience and career goals.

More about Associate International Clinical Research jobs
What cities are hiring for Associate International Clinical Research jobs? Cities with the most Associate International Clinical Research job openings:
What are the most commonly searched types of International Clinical Research jobs? The most popular types of International Clinical Research jobs are:
What states have the most Associate International Clinical Research jobs? States with the most job openings for Associate International Clinical Research jobs include:
What job categories do people searching Associate International Clinical Research jobs look for? The top searched job categories for Associate International Clinical Research jobs are:
Associate International Clinical Research jobs near you
Infographic showing various Associate International Clinical Research 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 23 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