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Summer Icon Clinical Research Jobs in Raleigh, NC

ICON

Director, Clinical Research Scientist

Raleigh, NC · On-site +1

Director, Clinical Research Scientist 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 ...

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Project Manager II, Laboratory

Raleigh, NC · Hybrid

Project Manager, II Labs- hybrid 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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Clinical Research Associate II

Raleigh, NC · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Cary, NC · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Raleigh, NC · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

ICON

Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist 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

Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist 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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Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist 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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Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist 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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Senior CRA

Cary, NC · On-site

Senior CRA Phase I Oncology NC 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 Scientist

Raleigh, NC · On-site +1

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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All JobsSummer Icon Clinical Research JobsSummer Icon Clinical Research Jobs in Raleigh, NC

Summer Icon Clinical Research information

See Raleigh, NC salary details

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How much do summer icon clinical research jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for summer icon clinical research in Raleigh, NC is $23.42, according to ZipRecruiter salary data. Most workers in this role earn between $19.62 and $24.09 per hour, depending on experience, location, and employer.

What is a Summer Icon Clinical Research position?

A Summer Icon Clinical Research position is typically an internship or temporary role offered during the summer months, where students or recent graduates work alongside experienced clinical researchers. The position involves participating in various stages of clinical trials, such as data collection, patient interaction, regulatory documentation, and analysis. These roles are designed to provide hands-on experience in clinical research, helping participants develop an understanding of clinical trial protocols, ethical considerations, and research methodologies. Summer Icon Clinical Research positions are valuable for those considering a career in medicine, pharmaceuticals, or scientific research.

What are the key skills and qualifications needed to thrive as a clinical research associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines, and typically hold a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are common requirements. Attention to detail, strong organizational skills, and effective communication make a candidate stand out in this role. These skills ensure accurate data collection, compliance with regulations, and successful coordination among research teams and study sites.

What are some common challenges faced by clinical research interns during a summer program, and how can they prepare for them?

Clinical research interns in summer programs often encounter challenges such as quickly adapting to complex regulatory protocols, managing large volumes of data, and balancing multiple tasks within tight timelines. To prepare, it's helpful to review basic clinical research methodologies, develop strong organizational skills, and familiarize yourself with commonly used software like REDCap or Excel. Proactive communication with supervisors and team members can also help clarify expectations and ensure smooth collaboration throughout the internship.

What is the difference between Summer Icon Clinical Research vs Summer Icon Clinical Research Coordinator?

AspectSummer Icon Clinical ResearchSummer Icon Clinical Research Coordinator
Primary RoleAssists in clinical trial activities, data collection, and site supportManages patient recruitment, schedules, and ensures protocol adherence
Required CredentialsTypically no formal certification, relevant coursework helpfulOften requires relevant healthcare or research certifications
Work EnvironmentResearch sites, laboratories, or clinical settingsClinical sites, hospitals, or research facilities
Employer & Industry UsagePharmaceutical companies, research institutionsHospitals, clinics, research organizations

In summary, Summer Icon Clinical Research roles focus on supporting clinical trials through data and site assistance, while Summer Icon Clinical Research Coordinators take on more responsibility in managing patient interactions and trial logistics. Both roles are essential in the clinical research process but differ in scope and responsibilities.

What are the most commonly searched types of Icon Clinical Research jobs in Raleigh, NC?

The most popular types of Icon Clinical Research jobs in Raleigh, NC are:

What are popular job titles related to Summer Icon Clinical Research jobs in Raleigh, NC?

For Summer Icon Clinical Research jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Summer Icon Clinical Research jobs in Raleigh, NC look for?

The top searched job categories for Summer Icon Clinical Research jobs in Raleigh, NC are:

Summer Icon Clinical Research jobs near you
Infographic showing various Summer Icon Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $48,709 per year, or $23.4 per hour.

Director, Clinical Research Scientist

ICON

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago

Job description

Director, Clinical Research Scientist
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 Do:
  • Development of protocols for clinical studies.

  • Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans.

  • Drafting of clinical scientific documents such as IND, IND amendments, Clinical Study Reports, Investigator Brochures, Annual Reports, and other health authorities submissions.

  • Responsible for providing clinical input into eCRF design, SAP, and TLFs.

  • Monitor, review, and summarize clinical safety and efficacy data in ongoing studies.

  • Collaborate with study team members to conduct timely and thorough review of study data using best practices and available tools to identify and evaluate data trends.

  • Will lead the clinical matrix teams for assigned studies, represent clinical development on project teams and serve as liaison to project teams, CRO's and others.

  • Provide clinical updates on assigned studies to Sr. management, Project Teams, Joint Project Teams and/or Steering Committees (if appropriate), Clinical sub-teams, internal strategy, and governance meetings, eDMC meetings, steering committees, advocacy groups, scientific advisory boards, and publications committees.

  • Liaise with cross functions on training of current studies, results, meeting with lead PIs/KOLs at conferences; present as needed.

  • Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.

  • Contribute to writing and review of study abstracts, posters, oral presentations, and manuscripts for assigned studies.

Your Profile:
  • Degree in scientific/life-sciences field. Pharm.D. or Ph.D. preferred.

  • Minimum of 4 - 6 years of experience in research with at least 3 or more years of clinical research/drug development experience are required for Director level.

  • Experience in Immunology field is required.

  • Ability to multi-task and work in a fast-paced environment.

  • Excellent written and oral communication skills.

  • Strong Analytical ability.

  • Ability to accommodate up to 20% travel or as business dictates.

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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