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Icon Clinical Research Jobs (NOW HIRING)

ICON

Home Health Study Manager

Blue Bell, PA · On-site

Home Health Study Manager - United States (Remote) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Icon plc

Home Health Study Manager

Blue Bell, PA · Remote

Home Health Study Manager - United States (Remote) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Icon plc

Medical Supply Kit Production Associate

Blue Bell, PA · On-site

$14.25 - $18.25/hr

Medical Supply Kit Production Associate - Blue Bell, PA (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Icon plc

At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are ...

ICON

Sr. Clinical Research Associate

Blue Bell, PA

Clinical Research Associate 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 ...

ICON

Senior Clinical Research Associate

Rochester, NY · On-site

$110K - $138K/yr

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

Icon plc

Sr. Clinical Research Associate

Blue Bell, PA · On-site

Clinical Research Associate 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 ...

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$49K

$107.3K

$189K

How much do icon clinical research jobs pay per year?

As of Sep 3, 2026, the average yearly pay for icon clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is an Icon Clinical Research?

An ICON Clinical Research job typically involves working for ICON plc, a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. Roles at ICON can range from clinical research associates and project managers to data analysts and regulatory specialists. Employees help design, manage, and monitor clinical trials to ensure they meet regulatory and ethical standards. These positions often require experience in clinical research, strong attention to detail, and adherence to Good Clinical Practice (GCP) guidelines.

What does a typical day look like for someone working at Icon Clinical Research?

A typical day at ICON Clinical Research often involves collaborating with cross-functional teams to oversee the progress of clinical trials, monitoring study data for accuracy, and ensuring all activities adhere to regulatory standards. You'll attend project meetings, communicate regularly with sponsors and investigators, and manage documentation and reporting tasks using specialized software. Depending on your specific role, you may also be responsible for site management, participant enrollment, or clinical data review. The work environment is fast-paced and supportive, offering opportunities for professional growth and advancement within the clinical research field.

What are the key skills and qualifications needed to thrive in the Icon Clinical Research position, and why are they important?

To thrive at ICON Clinical Research, you typically need a background in life sciences or a related field, experience with clinical trial processes, and strong analytical skills. Familiarity with industry-standard clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication help you excel in a collaborative research environment. These skills are crucial to ensure regulatory compliance, data integrity, and successful execution of clinical trials.

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Cities with the most Icon Clinical Research job openings:

What are the most commonly searched types of Icon Clinical Research jobs?

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Icon Clinical Research jobs near you
Infographic showing various Icon 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 $107,336 per year, or $51.6 per hour.

Home Health Study Manager

ICON

Blue Bell, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

Home Health Study Manager - United States (Remote)
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 have an incredible opportunity for a Home Health Study Manager to join ICON's Accellacare In-Home Care team. The Study Manager's primary responsibility is to coordinate and manage all contracted services in assigned studies, providing quality service, and exceeding the expectations of our customers. The Study Manager manages the key relationships and communication among all internal and external stakeholders involved in a study, keeping all stakeholders informed in a timely and professional manner about the progress and key events with the study. The Study Manager is expected to accurately identify issues and creatively resolve problems while correcting processes as needed.
This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Location: Eastern or Central Time Zone - United States (Remote)
What you will be doing:
  • Coordinate, administer, and document all study management activities while maintaining and adhering to study project plans and timelines
  • Train assigned staff (including subcontracted resources) and ensure staff is providing quality service
  • Provide support and guidance for all resources, including routine teleconferences to review progress to timelines, issue management, and information sharing
  • Contact necessary staff to ensure tasks are scheduled and have occurred per the required timelines
  • Review study documentation to ensure completeness, accuracy and timeliness, and seek or correct documentation, as needed
  • Ensure study information is updated and reports are reviewed and provided to the appropriate stakeholders according to expected timelines
  • Solicit information to support inquiries from all stakeholders
  • Support all internal and external team members in their efforts to support the study
  • Participate in and lead study team reviews
  • Act as the liaison between the sponsor, CRO, investigative site staff, laboratory, pharmacy and other internal and external personnel as the study requires
  • Represent department effectively and professionally in project calls, webinars, teleconferences, and meetings
  • Comply with ICH/GCP, IATA, HIPAA, and other appropriate regulations, policies and procedures
  • Ensure overall study deliverables and that contracted study visits are completed on schedule, documentation is timely, complete, and accurate, and lab samples are evaluable

Your profile:
  • 2+ years of experience as a Clinical Research Coordinator, Clinical Research Associate, or similar clinical research role coordinating study startup, operational activities, and study closeout processes
  • Exceptional attention to detail and organizational skills, with the ability to effectively manage multiple priorities and complex study activities concurrently
  • Strong problem-solving skills with the ability to quickly assess situations, identify solutions, and resolve operational challenges
  • Laboratory knowledge (preferred)
  • Bachelor's degree, preferably in a life sciences, healthcare, or related field

#LI-TP1
#LI-Remote
#LI-Accellacare
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

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