Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Clinical Trial Coordinator

ICON Clinical Research

Clinical Trial Coordinator

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

  • Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.

  • Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.

  • Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.

  • Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.

  • Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.

  • Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.

  • Basic knowledge of clinical trial processes and regulatory requirements is a plus.

  • Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.

  • Willingness to travel as required (approximately 25%)

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’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 family’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 family’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 ( to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’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 (

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Clinical Trial Coordinator in United States vacancy
  •  ...Clinical Trial Coordinator At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative... 
    Suggested
    Worldwide

    ICON plc

    Oregon State
    1 day ago
  •  ...SummaryWe are currently seeking an Experienced Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross functionally with...  ...and enrollment planning for global clinical trials. If you are an individual with a clinical... 
    Suggested
    Contract work
    Work from home

    Medpace

    Cincinnati, OH
    1 day ago
  •  ...specifications and user acceptance testing (UAT) Review incoming clinical data for completeness, consistency, and accuracy Generate,...  ...systems and software (EDC, CTMS, etc.) Familiarity with clinical trial processes and Good Clinical Practice (GCP) Experience with EDC... 
    Suggested
    Work at office

    Katalyst Healthcares & Life Sciences

    Dallas, TX
    1 day ago
  • Job-ID31742159Reference26-00089 Responsibilities Collect, enter, and manage clinical trial data using electronic data capture (EDC) systems. Perform data validation and query management to ensure data quality and compliance with study protocols. Assist in the development... 
    Suggested
    Interim role

    Katalyst Healthcares & Life Sciences

    Salt Lake City, UT
    1 day ago
  • $47k - $83k

     ...an accommodation or an alternative application process. Clinical Coordinator Full Time Cortland, NY, US Salary Range: $47,000.00 To...  ...Duties Coordinates screening and enrollment of clinical trial patients. Reviews physician-patient schedules and assesses... 
    Suggested
    Full time

    ADP

    Cortland, NY
    4 days ago
  •  ...Clinical Trial Coordinator Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in... 
    Local area
    Remote work
    Home office

    Thermo Fisher

    United States
    5 days ago
  •  ...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 7... 
    Local area
    Remote work
    Home office

    Thermo Fisher Scientific

    United States
    3 days ago
  •  ...Clinical Trials Data Coordinator Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los... 
    Hourly pay
    Full time
    Local area
    Remote work
    Shift work

    City of Hope

    United States
    2 days ago
  •  ...Clinical Data Coordinator I - Argentina At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global...  ...As a CDC I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement... 
    Remote work
    Worldwide

    ICON

    United States
    5 days ago
  • $27 - $33.65 per hour

     ...Clinical Data Coordinator Location: Detroit, MI (Hybrid: 3 Days Onsite / 2 Days Remote) About the Role Join a growing Hematology/Oncology research...  ...or Hematology research experience + Phase I clinical trial experience + SOCRA or ACRP certification (or interest in obtaining... 
    Contract work
    Temporary work
    Remote work

    Actalent

    Detroit, MI
    5 days ago
  •  ...poweredbytiny.com . The Opportunity Tiny Health is seeking a Clinical Coordinator to support the execution and operations of our growing...  ..., including protocol files, consent forms, and essential trial documents Ensure study activities follow HIPAA and... 
    Work experience placement
    Interim role
    Remote work

    Tiny Health

    Canada, KY
    2 days ago
  •  ...mitral valve replacement through pivotal clinical development, with a shared commitment to...  ...We are seeking a Clinical Coordinator to provide critical coordination and operational...  ...role that touches many aspects of clinical trial execution—from site documentation and clinical... 
    Work at office
    Local area
    Remote work
    Flexible hours
    Shift work

    4C Medical Technologies Inc

    Maple Grove, MN
    8 hours ago
  •  ...success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire...  ...development, clinical pharmacology, clinical trials, and commercial product manufacturing....  ...perform effectively Able to plan, coordinate, organize, and prioritize to meet deadlines... 
    Work at office
    Local area

    Quotient Sciences Limited

    Miami, FL
    5 days ago
  • $55k - $70k

     ...into trusted community access points for wellness screenings, clinical trials, and patient navigation. We partner with health systems,...  ...prescription revenue. Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical... 
    Remote work
    Flexible hours

    SiteLabs

    Doral, FL
    5 days ago
  • ERA Health Research seeks a Full-Time Regulatory and Data Coordinator I to support clinical trial operations in Redmond, WA. Hybrid work model with on-site training as needed. Responsibilities include regulatory document management, data integrity, and monitoring visit... 
    Full time
    Work at office
    Relocation package

    ERA Health Research

    Redmond, WA
    4 days ago
  • Moffitt is seeking a Clinical Trials Screening Coordinator I to support a Disease Site Program in a hybrid work setting. The role focuses on identifying eligible patients for trials, guiding them during screening, and ensuring safe, compliant trial progression within the... 
    Part time

    Moffitt

    Tampa, FL
    5 days ago
  •  ...Agent to join a dynamic team supporting clinical research recruitment efforts in Glendale...  ...high-volume inbound and outbound calls and coordination of study communications. The incumbent...  ...60-70 calls daily, assist potential trial volunteers, schedule appointments, and help... 
    Weekend work
    Afternoon shift

    Proclinical

    Glendale, CA
    4 days ago
  • Flourish Research seeks a Clinical Research Coordinator - Oncology for Valkyrie Clinical Trials in Walnut Creek, CA. The CRC will manage start-up, recruitment, consent, protocol mastery, and white-glove participant care, ensuring safety and data integrity per GCP/ICH guidelines... 
    Hourly pay

    Flourish Research

    Walnut Creek, CA
    5 days ago
  • TechMetro in Plano, Texas is seeking a Clinical Trial Coordinator to coordinate and manage trial activities in compliance with study protocols, GCP, and FDA/ICH regulations. This role involves collaborating with investigators, sponsors, and clinical staff to ensure smooth... 

    TechMetro

    Plano, TX
    4 days ago
  • Denverurology in Littleton, Colorado, is seeking a Clinical Research Coordinator to oversee research projects and provide quality service to both...  ...ideal candidate will have at least two years of clinical trial experience, preferably in Urology, and possess excellent communication... 

    Denverurology

    Littleton, CO
    4 days ago
  •  ...Clinical Trial Enrollment Coordinator - On-Site - US, Lenexa, KS 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 join us on... 

    ICON

    Lenexa, KS
    3 days ago
  •  ...leading research management organization in Detroit, MI, is looking for a Senior Clinical Research Coordinator. This role requires at least 5 years of experience managing clinical trials, particularly in a private setting. Responsibilities include ensuring adherence to... 

    DM Clinical Research

    Detroit, MI
    2 days ago
  •  ...Clinical Trial Payments/Clinical Trial Coordinator Our dynamic, clinical-stage, fast-paced medical device startup is developing novel technologies with the potential to significantly change population health. Every team member is a key contributor, directly impacting... 

    Custom Search Inc.

    Minneapolis, MN
    4 days ago
  • UW Medicine's Department of Emergency Medicine in Seattle seeks a Research Coordinator 2 to oversee day-to-day operations of a large pragmatic multi-center randomized trial across 17 U.S. hospital sites, primarily Harborview Medical Center. The RC2 will manage study start... 

    UW Medicine

    Seattle, WA
    4 days ago
  • Nicklaus Children's Research Institute in Miami, FL seeks a Lead Clinical Research Coordinator to independently coordinate multiple cancer studies within the Clinical Trials Office. You will manage recruitment, data handling, and regulatory tasks to ensure protocol compliance... 
    Full time
    Work at office

    Nicklaus Children's

    Miami, FL
    4 days ago
  • $65k - $70k

     ...Manager for the highest standards of operational delivery of the Clinical Trials for which the post holder is appointed to co-ordinate. This...  ...dictated for each study and GCP Private Practice Support: Coordinate all patient visits for monoclonal antibody infusions.... 
    Private practice
    Work at office
    Worldwide

    Re-Cognition-Health-Limited-

    Fort Worth, TX
    5 days ago
  • Advocate Health is seeking a Research Coordinator to coordinate sponsored clinical trials, assist physicians and research teams, and ensure protocol adherence across sites. The role involves study start-up, IRB submissions, patient recruitment and data collection in a fast... 

    Advocate Health

    Park Ridge, IL
    2 days ago
  • Paycom is hiring a Research Coordinator to manage end-to-end clinical trials, ensuring visits follow the protocol and regulatory standards. The role involves IRB correspondence, data collection, and maintaining trial documents in a compliant environment. The position emphasizes... 
    Work at office

    EyeHealth Northwest

    Portland, OR
    5 days ago
  •  ...Science University in Portland, OR, seeks a Therapeutic Intervention Senior Clinical Research Assistant in the Epilepsy Division, Department of Neurology to coordinate complex interventional trials with minimal supervision and ensure participant safety. The role involves... 

    OHSU

    Portland, OR
    5 days ago
  • $29.05 - $44.28 per hour

     ...opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Trials Screening Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to... 
    Work at office
    Remote work
    Relocation package
    Monday to Friday

    Moffitt Cancer Center

    Tampa, FL
    22 hours ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Clinical Trial Coordinator. Be the first to apply!