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Summer Icon Clinical Research Jobs (NOW HIRING)

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 ...

Clinical Research Coordinator

Johns Creek, GA ยท On-site

$22.50 - $30/hr

Clinical Research 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 ...

Clinical Research Coordinator

Johns Creek, GA ยท On-site

$22.50 - $30/hr

Clinical Research 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 ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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 ...

Senior CRA/ CRA II 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 ...

Dentist ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to ...

Clinical Research Nurse ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. We are currently ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Senior CRA 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 ...

Clinical Research Associate - East Coast 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 ...

Clinical Research Associate - Multi TA/Oncology - US 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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Summer Icon Clinical Research information

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$13

$24

$40

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

As of Jul 30, 2026, the average hourly pay for summer icon clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 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 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 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.
More about Summer Icon Clinical Research jobs
What cities are hiring for Summer Icon Clinical Research jobs? Cities with the most Summer Icon Clinical Research job openings:
What are the most commonly searched types of Icon Clinical Research jobs? The most popular types of Icon Clinical Research jobs are:
What states have the most Summer Icon Clinical Research jobs? States with the most job openings for Summer Icon Clinical Research jobs include:
Infographic showing various Summer Icon Clinical Research job openings in the United States as of July 2026, with employment types broken down into 20% Internship, 40% Full Time, 20% Part Time, 10% Temporary, and 10% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Nurse I

ICON Clinical Research

San Antonio, TX โ€ข On-site

Other

Medical, Life, Retirement, PTO

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift

ICON plc is a world-leading healthcare intelligence and clinical research organization. Weโ€™re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Nurse I to join our diverse and dynamic team. As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical trials, ensuring adherence to protocol requirements, and providing compassionate patient care throughout the research process.

Location: 100% on site- San Antonio TX 78209

Job Type : PRN / As Needed

Shift/Schedule : M-F 6 AM-2:30 PM

What you will be doing:

  • Assisting in the planning, implementation, and coordination of clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures (SOPs).

  • Conducting patient assessments, administering study treatments, and performing clinical procedures as required by the research protocol, while ensuring patient safety and compliance with ethical standards.

  • Collecting, recording, and maintaining accurate and complete data documentation, including medical histories, vital signs, adverse events, and laboratory results, in electronic case report forms (eCRFs) and study databases.

  • Collaborating with multidisciplinary teams, including investigators, study coordinators, and regulatory staff, to ensure efficient study conduct, participant recruitment, and retention throughout the duration of the trial.

  • Providing education and counseling to study participants and their families regarding study procedures, treatment regimens, and informed consent, while addressing any questions or concerns that may arise during the course of the study.

Your profile:

  • Must hold a current and valid Registered Nurse (RN) license in the state of Texas.

  • Minimum of 1-2 years of clinical nursing experience, preferably in a research or academic healthcare setting, with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.

  • Strong clinical assessment and critical thinking skills, with the ability to recognize and respond to changes in patient status and communicate effectively with healthcare professionals and study investigators.

  • Knowledge of regulatory requirements governing clinical research, including the International Council for Harmonization (ICH) guidelines and local regulatory requirements, with a commitment to upholding ethical standards and patient confidentiality.

  • Proficiency in electronic medical record (EMR) systems, clinical documentation, and data entry, with a high level of attention to detail and accuracy in recording patient information and study data.

  • Excellent interpersonal and organizational skills, with the ability to work independently and collaboratively in a fast-paced, multidisciplinary environment, while prioritizing competing demands and meeting project deadlines.

What ICON can offer you:

Our success depends on the quality of our people. Thatโ€™s why weโ€™ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your familyโ€™s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your familyโ€™s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. Weโ€™re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless โ€“ thereโ€™s every chance youโ€™re exactly what weโ€™re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply