Project Manager II, Laboratory

About the Opportunity

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

At ICON, it’s our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

Responsibilities

• Act as the sponsor's main contact person in all matters regarding our central laboratory services.
• Review newly assigned protocols and Amendments.
• Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate).
• Ensure adherence to the protocol specific monitoring plan.
• Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained.
• Provide Sponsors with study management reports as required and agreed.
• Proactively monitor study budget through monitoring of Protocol Tracking reports and other tools provided to assist.
• Set the timelines for and monitor the progress of shipment requests for storage samples and verify data.
• Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defenses or Face to Face Governance meetings.
• Serve as a leader, mentor and consultant to more junior team members in resolving issues or questions as they arise.
• Serve as a gateway for escalation of PM issues to PM Manager and Senior/Executive Management.

About You

What You Need

• In depth proven experience working in a clinical laboratory, clinical trials, or customer management/account management role in a life sciences related organization.
• Prior relevant experience successfully performing a Project Management role in a service area serving clinical trials.
• Bachelor's degree or local equivalent in Science, Business or related Field and/ or an alternative combination of experience, education, and training.

Benefits

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

About Company

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply.