ZipRecruiter

Log In

1

Clinical Study Jobs (NOW HIRING)

ICON

Clinical Study Specialist

Warren, NJ · On-site

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring ...

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 ...

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 ...

Kps-Life

Sr. Clinical Study Lead (Hybrid)

Cambridge, MA · On-site

On Assignment Sr. Clinical Study Lead (Hybrid) KPS Life is hiring a Senior Clinical Study Lead (Sr. CSL) to be fully dedicated to our sponsor client and located on site 3 days per week in either ...

New

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 ...

University of Utah

Clinical Study Coordinators

Campus, IL · On-site

$22K - $51K/mo

Details Open Date 08/17/2026 Requisition Number PRN45944B Job Title Clinical Study Coordinators Working Title Clinical Study Coordinators Career Progression Track P00 Track Level P2 - Developing, P1 ...

University of Utah

Clinical Study Coordinators

Campus, IL · On-site

$22K - $51K/mo

Details Open Date 08/17/2026 Requisition Number PRN45944B Job Title Clinical Study Coordinators Working Title Clinical Study Coordinators Career Progression Track P00 Track Level P2 - Developing, P1 ...

Icon plc

Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring ...

Icon plc

Clinical Study Specialist

Cambridge, MA · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring ...

Icon plc

Clinical Study Specialist

New York, NY · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

BeiGene USA

Regional Clinical Study Senior Manager

Acts as regional lead for multiple studies across an indication or across a program as required * Leads the regional clinical operations team (including external partners working on a regional level ...

previous page

Showing results 41-60

All JobsHealthcare JobsClinical Study Jobs

clinical study information

See salary details

$22K

$125.3K

$206K

How much do clinical study jobs pay per year?

As of Sep 12, 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 is a clinical study?

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 the key skills and qualifications needed to thrive as a clinical study coordinator?

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.

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 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.

Do clinical studies pay well?

Clinical study roles, such as clinical research coordinators or assistants, typically offer moderate pay that varies based on experience, location, and the complexity of the study. Entry-level positions may start at minimum wage or slightly above, while experienced professionals or those with specialized skills can earn higher salaries, often supplemented by benefits and overtime opportunities.

What jobs are there in clinical studies?

Jobs in clinical studies include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research facility, hospital, or pharmaceutical company, with schedules varying from full-time to part-time depending on the role.
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:

What are popular job titles for Clinical Study?

Popular job titles for Clinical Study:

clinical study jobs near you
Infographic showing various Clinical Study job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Clinical Study Specialist

Cambridge, MA • Hybrid

410 ICR United States USA
See more jobs at 410 ICR United States USAexternal

$62K - $77K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago

Job description

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA))

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.


What you will be doing

  • Organizes and delivers analyzable reports and metrics to the clinical study lead

  • Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings

  • Collates data for assessments such as feasibility and site selection and reviews site usability database

  • Contributes to review of study documents such as informed consent forms, case report forms and facilitates study document reviews per company standard operating procedures

  • Compiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders

  • Collates materials for training and investigator meetings

  • Tracks site activation, enrolment and monitoring visits to projected plans, and escalate any issues or delays with site activation or deviations from monitoring plan

  • Monitors and updates investigator/site status for the trial, and supports with clinical trial registry postings

  • Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance

  • Ensures scheduled reports are received (i.e. 1572 reportable changes, financial disclosure form)

  • Manages and maintains team SharePoint and/or shared drive sites, as needed

  • Communication with sites as directed and maintains site contact information

  • Contributes to line listings review for Blind Data Review Meeting (BDRM)

  • May manage or contribute to oversight of Third Party Vendors (TPV)

  • Tracks and monitors close out activities – study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and CRA close-out visits

  • Participates in Standard Operating Procedures (SOPs) revisions or departmental initiatives

  • Proactively recommends process improvement initiatives for the department

Your profile

  • Must have a Bachelor's Degree

  • Must have a minimum of 2 years industry related work experience

  • Experience supporting global trials (NA, LAM, EU, APAC, India)

  • Experience working in TMF, CTMS, Sharepoint,

  • Excels in written and verbal communications

  • Self-starter, can work independently with minimal oversight, solution-oriented

  • ICF review experience

  • General competency: powerpoint/excel skills, meeting minutes

  • Vendor management/oversight experience a plus

  • Must be open to hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA


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

$62,376.00-$77,970.00

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