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Clinical Study 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 ...

Global Channel Management, Inc.

$57/hr

Qualifications Clinical Study Manager needs 5 years relevant experience is required with a BSc, 3 years with a MS/MPH, or 2 years with PharmD/PhD/MD Clinical Study Manager requires: * Phase II/III ...

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 ...

PSI CRO

Clinical Study Coordinator

Cleveland, TN

We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Site/Study Coordinator supports a medical institution in clinical trial ...

DiaSorin

Clinical Study Coordinator

Austin, TX

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of analytical and clinical studies involving Luminex in vitro diagnostic devices, planning and execution of ...

Danaher

Senior Clinical Study Manager

Chaska, MN · On-site

$135K/yr

The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...

DiaSorin

Clinical Study Coordinator

Austin, TX · On-site

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of analytical and clinical studies involving Luminex in vitro diagnostic devices, planning and execution of ...

People Make Us

Clinical Study Manager

Durham, NC · On-site

Provide operational leadership, coordination, and oversight for assigned clinical studies. Ensure studies are conducted in compliance with ICH/GCP guidelines, regulatory requirements, company SOPs ...

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Clinical Study information

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$22K

$125.3K

$206K

How much do clinical study jobs pay per year?

As of Jul 13, 2026, the average yearly pay for clinical study in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What can you do with a clinical studies degree?

A clinical studies degree prepares individuals for roles in clinical research, such as clinical research coordinator, clinical data manager, or research associate. These positions involve managing trials, collecting and analyzing data, and ensuring compliance with regulatory standards, often requiring knowledge of Good Clinical Practice (GCP) and familiarity with research tools and protocols.

What are clinical studies?

Clinical studies are research investigations conducted with human volunteers to evaluate the safety, effectiveness, and side effects of medical treatments, drugs, devices, or interventions. These studies follow strict scientific and ethical guidelines and are usually carried out in several phases before a treatment can be approved for widespread use. Clinical studies help determine whether new approaches to prevention, diagnosis, or therapy are safe and effective for people. Participation in clinical studies is voluntary and can contribute to advancements in medical science.

What are some common challenges faced when managing multiple clinical studies simultaneously?

Professionals involved in clinical studies often juggle several projects at once, which can present challenges such as balancing competing timelines, ensuring regulatory compliance across studies, and coordinating with diverse teams. Effective project management, clear communication, and strong organizational skills are key to addressing these challenges. Utilizing project management tools and maintaining detailed documentation can help keep studies on track and reduce the risk of errors or delays.

What does a clinical study do?

A clinical study involves researching new medical treatments, drugs, or devices to determine their safety and effectiveness. Clinical study professionals, such as clinical research coordinators or investigators, manage the process, collect data, and ensure compliance with regulatory standards throughout the trial.

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

AspectClinical StudyClinical Research Coordinator
CredentialsOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are advantageous
Work EnvironmentConducted in hospitals, clinics, or research facilities; involves direct patient interaction and data collectionWorks in research sites, hospitals, or clinics; manages study logistics and coordinates between teams
Employer & IndustryPharmaceutical companies, academic institutions, CROsResearch institutions, hospitals, pharmaceutical companies

While both roles are integral to clinical research, a Clinical Study typically refers to the overall research process or specific studies, whereas a Clinical Research Coordinator is a professional who manages and oversees the day-to-day operations of clinical trials. Understanding these distinctions helps in choosing the right career path or job search focus.

How much money can I make doing clinical trials?

Clinical study participants typically earn between $50 and $500 per visit, depending on the trial's complexity, duration, and required procedures. Compensation varies based on factors such as the type of study, location, and whether the trial involves invasive procedures or longer commitments.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related roles. Entry-level roles in clinical research may include Clinical Trial Assistant or Clinical Research Coordinator, with CRAs often needing a bachelor's degree and knowledge of Good Clinical Practice (GCP) guidelines. Advancement to a CRA position often involves gaining experience and sometimes obtaining certifications like the CCRP or RAC.

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 guidelines like GCP, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as CCRC or CCRA is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating multiple tasks and interacting with diverse stakeholders. These skills ensure compliance, accurate data collection, and smooth trial operations, which are vital for the integrity and success of clinical studies.
More about Clinical Study jobs
What cities are hiring for Clinical Study jobs? Cities with the most Clinical Study job openings:
What are the most commonly searched types of Clinical Study jobs? The most popular types of Clinical Study jobs are:
What states have the most Clinical Study jobs? States with the most job openings for Clinical Study jobs include:
Clinical Study jobs near you
Clinical Study Coordinator

Clinical Study Coordinator

ICON

Blue Bell, PA • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 13 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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