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Icon Plc Jobs in Raleigh, NC (NOW HIRING)

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

Senior Project Manager, COA-ICON- US Remote (East Coast) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

Feasibility Informatics Manager 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 ...

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

Feasibility Informatics Manager 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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How much do icon plc jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for icon plc in Raleigh, NC is $32.85, according to ZipRecruiter salary data. Most workers in this role earn between $29.42 and $36.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at ICON plc?

To thrive as a Clinical Research Associate at ICON plc, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for success in this role. These skills and qualifications are vital to ensuring clinical trials are conducted accurately, ethically, and in compliance with regulatory standards.

What is ICON plc?

ICON plc is a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. The company specializes in clinical research and provides a wide range of services including clinical trial management, consulting, and laboratory services. ICON plc helps organizations bring new medicines and medical devices to market by managing and conducting clinical studies and ensuring regulatory compliance. Founded in 1990 and headquartered in Dublin, Ireland, ICON operates in over 40 countries worldwide.

What are the typical responsibilities of a Clinical Research Associate at ICON plc?

As a Clinical Research Associate (CRA) at ICON Plc, your primary responsibilities include monitoring clinical trial sites, ensuring compliance with study protocols, and maintaining accurate documentation. You'll frequently collaborate with site staff and cross-functional teams to resolve any issues and support patient safety and data integrity. The role requires regular travel to trial locations, attention to regulatory requirements, and effective communication skills. Your contributions are vital for keeping studies on track and ensuring high-quality, reliable results for sponsors.

What is the difference between Icon Plc vs Clinical Research Associate?

AspectIcon PlcClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or CRA are commonRequires similar degrees; certifications like CCRA or CRA are often necessary
Work EnvironmentGlobal clinical trial sites, offices, and remote settingsMonitoring clinical trials at sites, coordinating with sponsors and sites
Employer & Industry UsageContract research organization (CRO) providing clinical trial servicesRole within CROs, pharmaceutical companies, or biotech firms

Icon Plc is a leading CRO that employs Clinical Research Associates (CRAs) to monitor and manage clinical trials. Both roles require similar qualifications and work in comparable environments, often within the pharmaceutical and biotech industries. The main difference lies in the company branding and specific project assignments, but their responsibilities and credentials overlap significantly.

What cities near Raleigh, NC are hiring for Icon Plc jobs? Cities near Raleigh, NC with the most Icon Plc job openings:
Infographic showing various Icon Plc job openings in Raleigh, NC as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 3% Contract, and 2% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $68,325 per year, or $32.8 per hour.

Oncology Scientific Lead, Med Com (Associate Scientific Dir)

Icon plc

Raleigh, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 18 days ago


Job description

Scientific Lead - Medical Communications

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.


ICON Global Medical Communications (GMC) is looking for a passionate, and inspiring Scientific Lead to join our team. As a Scientific Lead you will build on the responsibilities of a Sr. Medical Writer and take on additional project-level content development and management responsibilities. This role encompasses high-level writing, peer-review of project deliverables, strategic support and client engagement as determined by the respective aligned account leaders.

Your primary responsibility will be independent approval of scientific/clinical content for assigned projects/tasks.Your oversight will include review of assigned materials for accuracy and quality, mentoring and developing junior writing staff, and contributing scientific and therapeutic insights. The Scientific Lead will work closely with the Scientific Manager to support members of the client account team as directed.

This person should have prior experience with background researching, developing, and high-quality writing for the diverse array of deliverables within medical publications and medical communications.

What You'll Be Doing:

Content oversight and quality control responsibilities are including but not limited to:

  • Review work of other internal writers, including junior medical writers
  • Product/therapy area information and strategic insight pertinent to the assigned projects
  • Fact checking assigned manuscripts
  • Collaboration with the Scientific Manager and account managers to help ensure adherence to agreed-upon timelines
  • Helping to oversee all aspects of project development from initiation to completion, including escalating issues with financial impacts

Scientific/medical writing and content-development support:

  • Writing manuscripts, posters, abstracts, slide decks, and/ or other deliverables requiring scientific/medical writing support
  • Identify and obtain required/helpful background materials, including from client
  • Collaborating with editorial support staff to provide necessary background and technical information
  • Participate in onboarding and mentoring of new and junior medical writers
  • Conduct background research and writing support for new business proposals and organic growth opportunities

What you need:

  • Advanced degree, preferably PhD but PharmD and MD may also be considered
  • Prior experience in a medical publications/medical communications agency
  • Minimum of 4-5 years' experience of high-level content development and management actives in the medical communication agency setting
  • 3 years as a Senior Medical Writer, strongly preferred
  • CMPP/MAPPS Certification, great to have
  • Demonstrable history of relevant high-level writing support and review (e.g, while at a medical communications agency), including proficiency with ICMJE and GPP guidelines; reviewing and interpreting scientific and technical journal content; knowledge of diverse prescribed styles and formats
  • People management and client relationship skills preferred
  • Ability to work efficiently with network directories/databases
  • Familiarity and ability to work with industry standard resources (e.g., PubMed/Medline, clinicaltrials.gov, various market intelligence/data analytic providers, etc)
  • Ability to work with cross-functional teams (e.g., editorial/library services, graphics/digital services, presentations support, etc)

#LI-KM3

#LI-REMOTE


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 requesthere.

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