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Clinical Trial Support Specialist
2 weeks ago
Company Overview
ICON plc is a world-leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence.
We're committed to shaping the future of clinical development, and we welcome talented individuals to join our diverse and dynamic team.
Salary and Benefits
Our compensation package includes a competitive salary, along with various annual leave entitlements and a range of health insurance offerings.
Additionally, ICON offers flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.
Job Description
We are seeking a Laboratory Support Coordinator to join our team, who will play a critical role in providing logistical and operational support for laboratory services in clinical trials.
The successful candidate will be responsible for coordinating laboratory activities, managing sample workflows, and collaborating with various departments to ensure efficient and timely sample processing and data management.
Key Responsibilities:
- Coordinating laboratory operations, including sample receipt, processing, and shipment in alignment with study protocols.
- Working closely with clinical trial teams to ensure laboratory activities are executed according to timelines and regulatory standards.
- Monitoring and maintaining laboratory equipment, supplies, and inventory to support ongoing clinical trials.
- Ensuring proper documentation and tracking of laboratory data to meet compliance and quality standards.
- Collaborating with external vendors and laboratories to manage outsourcing needs and facilitate sample logistics.
Required Skills and Qualifications
The ideal candidate will possess a Bachelor's degree in a relevant scientific discipline, such as biology, chemistry, or clinical laboratory science.
A minimum of experience working in a laboratory setting, preferably within a clinical trials or pharmaceutical environment, is required.
The selected individual must demonstrate strong organizational and multitasking skills, with the ability to manage multiple projects simultaneously.
Excellent communication and interpersonal skills are essential, with the ability to collaborate across cross-functional teams and external partners.
Diversity, Inclusion & Belonging
At ICON, diversity, inclusion & belonging are fundamental to our culture and values.
We're dedicated to providing an inclusive and accessible environment for all candidates and employees.
Equal Opportunities Employer
ICON is an equal opportunities employer and welcomes applications from all qualified individuals.
