Project Leader

ICON plc • Portland, OR

5d • Onsite

About The Position

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. At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Requirements

• Associate’s Degree in relevant biological disciplines/analytical chemistry.
• A minimum of 5 years’ experience successfully performing a laboratory Scientist role or a minimum of 7 years’ experience of study related matters, GLP or other Quality systems, analytical procedures and general laboratory experience.
• Good written record keeping and verbal communication skills.
• Ability to accurately follow and communicate precise written and verbal instructions

Nice To Haves

• Bachelor’s Degree or equivalent in relevant biological disciplines /analytical chemistry preferred.

Responsibilities

• Assist in development and validation of analytical methods to support regulatory studies and manage sample analysis on preclinical and clinical specimens.
• Manage analytical studies to ensure that bioanalysis is well coordinated with the in life study, and that samples are appropriately tracked throughout the lifetime of the study and any agreed storage period.
• Monitor and evaluate the projects progress with respect to milestones, budgets and timelines.
• Work with laboratory management to ensure that appropriate resources are available to complete the study to timeline.
• Obtain all client specific documents required for the analysis.
• Maintain records of work conducted in a timely and consistent manner, sufficient to allow real-time tracking of the deliverables, including tracking of revenue and resources associated with assigned studies.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree