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Clinical Study Coordinator Jobs (NOW HIRING)

ICON

Clinical Study Coordinator

Blue Bell, PA · On-site

Clinical Study Coordinator 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 ...

Icon plc

Clinical Study Coordinator

Blue Bell, PA · On-site

Clinical Study Coordinator 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 ...

Icon plc

Clinical Study Coordinator

Washington, DC · On-site

Clinical Study Coordinator 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 ...

Propedix, Inc.

Clinical Study Coordinator

Milford, MA · On-site

$25 - $30/hr

Clinical Study Coordinator (Consultant) About the Company: Propedix is a biopharma and consumer health company dedicated to advancing innovative treatments in healthcare. Our flagship product ...

City of Hope

Clinical Study Coord

Duarte, CA

Clinical Study Coordinator - Clinical Research (On-Site) Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes ...

City of Hope

Clinical Study Coord

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coordinator

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site) Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes ...

City of Hope

Clinical Study Coordinator

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site) Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes ...

PSI CRO

Clinical Study Coordinator

Tulsa, OK

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and ...

Milestone One

Clinical Study Coordinator

Tulsa, OK

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and ...

City of Hope

Clinical Study Coord

Duarte, CA

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

Icon plc

Clinical Study Coordinator

Washington, DC

Clinical Study Coordinator 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 ...

City of Hope

Clinical Study Coord

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coord

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coord

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site) Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes ...

City of Hope

Clinical Study Coordinator

Zion, IL · On-site

Clinical Study Coordinator About City of Hope, City of Hope's mission is to make hope a reality for all touched by cancer and diabetes. Founded in 1913, City of Hope has grown into one of the largest ...

PSI CRO

Clinical Study Coordinator

Cleveland, TN

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and ...

PSI CRO

Clinical Study Coordinator

Tulsa, OK · On-site

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and ...

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How much do clinical study coordinator jobs pay per year?

As of Jul 13, 2026, the average yearly pay for clinical study coordinator in the United States is $67,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,500.00 and $78,500.00 per year, depending on experience, location, and employer.

What does a clinical study coordinator do?

A clinical study coordinator manages and oversees clinical trials to ensure they follow protocols, regulatory requirements, and good clinical practice. They coordinate participant recruitment, collect and record data, and communicate with research teams, often using electronic data capture systems. Strong organizational skills and knowledge of regulatory guidelines are essential for this role.

Who makes more, CRC or CRA?

In the clinical research field, Clinical Research Associates (CRAs) generally earn higher salaries than Clinical Research Coordinators (CRCs) due to their greater responsibilities in monitoring and overseeing clinical trials. CRAs often have more experience, specialized training, and may work remotely or travel frequently, which can contribute to higher compensation. Salary differences can vary based on experience, location, and employer, but overall, CRAs tend to have higher earning potential than CRCs.

What is the difference between Clinical Study Coordinator vs Clinical Research Associate?

AspectClinical Study CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences or related field; certifications like CCRP are a plusOften a bachelor's degree in life sciences; certifications like CCRP or RAC are common
Work EnvironmentConducts site visits, manages study activities at clinical sitesMonitors multiple sites remotely or on-site, ensuring protocol compliance
Employer & Industry UsageHospitals, clinics, research sitesPharmaceutical companies, CROs, biotech firms

While both roles support clinical research, Clinical Study Coordinators focus on managing day-to-day site activities, whereas Clinical Research Associates primarily monitor and oversee multiple sites to ensure regulatory compliance and data integrity.

What are some common challenges Clinical Study Coordinators face when managing multiple studies at once?

Clinical Study Coordinators often juggle several studies simultaneously, which requires strong organizational and time-management skills. Challenges include prioritizing tasks, ensuring regulatory compliance across different protocols, and keeping accurate documentation for each study. Effective communication with investigators, sponsors, and participants is essential to prevent misunderstandings and maintain study timelines. Utilizing project management tools and maintaining up-to-date records can help coordinators stay on track and reduce stress.

Is CRC an entry level position?

A Clinical Study Coordinator (CRC) is often considered an entry-level position in clinical research, typically requiring a bachelor's degree and some familiarity with Good Clinical Practice (GCP) guidelines. However, experience and certifications like the Certified Clinical Research Coordinator (CCRC) can enhance job prospects and responsibilities.

What is the salary of a clinical research coordinator?

The salary of a clinical research coordinator typically ranges from $50,000 to $70,000 annually, depending on experience, location, and the complexity of the studies they manage. Entry-level coordinators may earn less, while those with specialized skills or certifications can earn higher salaries. Many coordinators also receive benefits such as health insurance and paid time off.

What are the key skills and qualifications needed to thrive as a Clinical Study Coordinator, and why are they important?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, IRB submission processes, and Good Clinical Practice (GCP) certification is highly valued. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating study teams and liaising with stakeholders. These abilities ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, safeguarding both data integrity and participant safety.
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Clinical Study Coordinator jobs near you
Clinical Study Coordinator

Clinical Study Coordinator

ICON

Blue Bell, PA • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Clinical Study Coordinator
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 Clinical Study Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
  • Collaborating with cross-functional teams to develop and implement clinical trial protocols.
  • Coordinating and overseeing the execution of clinical studies, ensuring adherence to protocols and regulatory requirements.
  • Managing study timelines, budgets, and resources effectively.
  • Facilitating communication between investigative sites, sponsors, and internal teams.
  • Ensuring data accuracy and completeness through regular monitoring and quality control activities.

Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
  • Bachelor's degree in a relevant scientific discipline.
  • Proven experience as a Clinical Study Coordinator or in a similar role.
  • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
  • Strong organizational and multitasking skills.
  • Excellent communication and interpersonal abilities.

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
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