Project Manager I EDS
- Whitesboro
- ICON Full Service & Corporate Support
- Program Management
- Office Based
About the role
This vacancy has now expired. Please see similar roles below...
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.
Monitor and evaluate bioanalytical projects progress with respect to milestones, budgets and timelines.
• Manage bioanalytical studies to ensure that bioanalysis is well coordinated with in life study phases, and that samples are appropriately tracked throughout the lifetime of the study and any agreed storage period.
• 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; i.e., study protocol, randomization lists, COA, demographics, etc. Review protocol and amendments to assure adherence to specifications and regulatory requirements.
• Prepare analysis plans suitable to the client’s needs, as specified by contract, and obtain client approval of these.
• Work with laboratory operations to ensure compliance to study and validation plans.
• Provide Sponsors with regular updates, forecasting and communicating study progress. Timely reporting of any significant deviations.
• Ensure that project delivery, reporting specifics, and timelines as agreed are met. Inform laboratory operations, DM and QC/QA of deadlines.
• Maintain records of work conducted in a timely and consistent manner, sufficient to allow real-time tracking of deliverables, including tracking of revenue and resources associated with assigned studies.
• Identify changes to scope of work as defined by contract and ensure that change orders are processed prior to work being executed.
• Review and approve all data in accordance with direction documents and ensure results are documented accurately, completely and compliant with GxP regulations and SOPs. Initiate investigations and event deviations as necessary.
• Proactively identify possible/potential implications of unusual results, work with laboratory staff to investigate and report findings.
• Prepare reports of the work conducted, address all QA findings and provide QA draft report in line with the terms and conditions stated in the signed contract.
• Ensure that all documentation is appropriately archived on completion of the study.
• *Review and approve laboratory notebooks and other analytical data as required.
• Maintain awareness of and adherence to all current SOPs.
• *Work in compliance with GLP/GCP.
• Any other duties related to maintaining the provision of the Laboratory Analytical Services.
• A suggested minimum of 3 years’ experience in a laboratory or project management role, at discretion of hiring manager. Also, minimum education requirement is Associate’s degree.
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
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Salary
Location
Netherlands, Assen
Department
Full Service - Development & Commercialisation Solutions
Location
Assen
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Program Management
Job Type
Temporary Employee
Description
At ICON Plc, we are a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, medical device, and government organizations. With a presence in over 9
Reference
JR118498
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia Cairns