Job detail

Clinical Associate - CTA

ICON plc

#Regulatory Guidelines #Clinical Operations #Data Management #CRO #Pharmaceutical #Protocol Adherence #Site Initiation #Biotechnology #Biometrics

Quick overview

Support the design, implementation, and management of clinical trials by coordinating site initiation and patient recruitment. Maintain comprehensive study documentation and collaborate with cross-functional teams to ensure regulatory compliance and data accuracy.

Requirements summary

Requires a bachelor's degree in a scientific or healthcare field and previous experience in clinical research, preferably within the pharmaceutical or CRO industry. Candidates must possess strong organizational skills and a willingness to travel as needed.

bachelor degreeTime ManagementProblem SolvingInterpersonal CommunicationRegulatory ComplianceData CollectionCross-functional CollaborationPatient RecruitmentClinical CoordinationClinical Trial MonitoringStudy Documentation

Job description

Clinical Associate - CTA 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 CTA at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do: You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include: Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.
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 in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
Willingness to travel as needed 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 ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide.
You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.
If you’re as driven as we are, join us.
You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
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Clinical Associate - CTA

Clinical Associate - CTA

Quick overview

Requirements summary

Job description

Benefits

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