Study Coordinator
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What you'll do
- Collaborating with cross-functional teams to develop and implement clinical trial protocols.
- Coordinating and overseeing the execution of clinical studies, ensuring adherence to protocols and regulatory requirements.
- Managing study timelines, budgets, and resources effectively.
- Facilitating communication between investigative sites, sponsors, and internal teams.
- Ensuring data accuracy and completeness through regular monitoring and quality control activities.
What they're looking for
- Bachelor's degree in a relevant scientific discipline.
- Proven experience as a Clinical Study Coordinator or in a similar role.
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Strong organizational and multitasking skills.
- Excellent communication and interpersonal abilities.
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 Study 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 research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
- Collaborating with cross-functional teams to develop and implement clinical trial protocols.
- Coordinating and overseeing the execution of clinical studies, ensuring adherence to protocols and regulatory requirements.
- Managing study timelines, budgets, and resources effectively.
- Facilitating communication between investigative sites, sponsors, and internal teams.
- Ensuring data accuracy and completeness through regular monitoring and quality control activities.
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 scientific discipline.
- Proven experience as a Clinical Study Coordinator or in a similar role.
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Strong organizational and multitasking skills.
- Excellent communication and interpersonal abilities.
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.
Salary Range
-Are you a current ICON Employee? Please click here to apply
Company
Company facts come from this company's own listings. We only show what the postings themselves carry.