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Clinical Trial Specialist

ICON Strategic Solutions

Job Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organization, 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.

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As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

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This position is onsite in McComb, MS 2-3 times/week.

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What You Will Do:

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

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Key responsibilities include:

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  • Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
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  • Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
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  • Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
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  • Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
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  • Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.
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Your Profile:

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

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Required qualifications and experience:

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  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
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  • Previous experience working in clinical research or healthcare settings preferred.
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  • Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
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  • Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
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  • Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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Rewards & Benefits

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ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

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Benefits may include:

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  • Competitive base salary and performance related incentives
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  • Health and wellbeing programs including medical, dental, and vision coverage where applicable
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  • Retirement and pension plans
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  • Life assurance and disability coverage
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  • Employee assistance programs and wellbeing resources
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  • Learning and development opportunities through structured training and career pathways
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Benefits may vary depending on role and location.

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Inclusion and Accessibility

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ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

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If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

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

Vacancy posted 24 days ago
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