Clinical Research Coordinator
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What you'll do
- Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
- Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
- Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
- Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.
What they're looking for
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
- Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
- Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.
Nice to have
- Previous experience working in clinical research or healthcare settings preferred.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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.
As a Clinical Research Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
Your role will involve delivering clinical coordination work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
- Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
- Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
- Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
- Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.
Your Profile:
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Previous experience working in clinical research or healthcare settings preferred.
- Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
- Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
- Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.
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
Company
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