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Full-time

Project Manager II, Laboratory

Competitive

Farmingdale, NYScience & PharmaceuticalPosted 13d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

Competitive

Posted

13 days ago

Job description

ICON plc is hiring a Project Manager II, Laboratory, to manage client relationships and day-to-day clinical laboratory studies. The role coordinates study setup, protocol and study documentation, client communications, budgets, timelines, and representation of ICON at client meetings.

Responsibilities

The Project Manager, Labs will ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Laboratory Services (ILS), including the setup and day-to-day management of studies, attend and represent ILS at Client meetings, manage studies in accordance with Good Clinical Practice, provide Clients with regular study updates and communicate study progress to Clients and PM Leadership in a responsible and professional manner

Act as the sponsor's main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department

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)

Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Prepare and QC clinical study specific materials

Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure

Provide Sponsors with study management reports. Provide client with support on ICOLabs system. Inform team leader about study progress

Proactively monitor study budget

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 Initiations

Develop new tools, train new employees

Performs additional relevant responsibilities as requested by management

Benefits

Hybrid work arrangement.

Various annual leave entitlements.

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

Life assurance.

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Company

Clinical research organization providing outsourced drug and device development services

Dublin, Dublin, IRL

https://www.iconplc.com/

Founded in 1990

10001+ employees

Qualifications

Bachelor's degree or local equivalent in Science, Business or related Field

Minimum of 2 years of experience working in a clinical laboratory, clinical trials, or customer management/account management role in a life science related organization

Minimum of 2 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture

Working familiarity with Word, Excel, PowerPoint

Minimum of 2 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture.

Required skills

Account Management, Clinical Laboratory, Clinical Trials, Customer Management, Microsoft Excel, Microsoft PowerPoint, Microsoft Word

Preferred skills

Project Management

Experience

2+ years

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