Hours: Full-time, 40 hours per week, Dayshift: Monday - Friday, Tuesday-Friday, and Saturday shift available as optional.
Clinical Sample Processor Position Overview:
We are currently seeking a Clinical Sample Processor I to join our diverse and dynamic team. As a Clinical Sample Processor I at ICON, you will play a pivotal role in the collection, processing, and tracking of clinical trial samples to ensure accurate and timely analysis, contributing to the advancement of Innovative treatments and therapies.
Responsibilities of the role:
Collecting, receiving, and logging clinical trial samples according to study protocols and standard operating procedures (SOPs).
Processing samples using various laboratory techniques and equipment, ensuring proper handling and storage conditions.
Performing data entry and maintaining accurate records of sample receipt, processing, and distribution.
Participating in inventory management activities, including ordering supplies and maintaining stock levels.
Assisting with the disposal of samples and hazardous waste in compliance with regulatory requirements.
Qualifications for the role:
Bachelor's degree in a scientific discipline or related field, or equivalent combination of education and experience.
Previous experience in a laboratory or clinical research setting preferred.
Familiarity with laboratory techniques and equipment used for sample processing preferred.
Strong attention to detail and ability to follow standard operating procedures (SOPs) and safety guidelines.
Excellent organizational and time management skills with the ability to prioritize tasks and meet deadlines.
Clinical Sample Processor Position and responsibilities Overview:
We are currently seeking a Sample Management Coordinator I to join our diverse and dynamic team. As a Sample Management Coordinator I at ICON, you will be responsible for the proper handling, tracking, and documentation of clinical trial samples. Your work will play a crucial role in ensuring the accurate and timely management of biological samples, contributing to the success of clinical research studies.
What You Will Be Doing:
Coordinating the receipt, tracking, and storage of clinical trial samples in compliance with protocols and regulatory requirements.
Maintaining accurate documentation of sample collection, storage conditions, and chain of custody records.
Ensuring proper labeling and inventory of biological samples, and supporting the timely distribution of samples to laboratories for analysis.
Collaborating with clinical teams, laboratory personnel, and logistics providers to ensure timely and efficient sample management.
Assisting with sample-related queries and resolving discrepancies in sample tracking or documentation.
Contributing to process improvement initiatives in sample management and ensuring compliance with quality standards.