Ref #: 30070

Employment type: Permanent - Full-Time

Location: Poland

Posted: 17-Jun-2021

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.


Overview:
In this role you will line manage our FSP team of Regional Clinical Trial Managers and perform oversight in fulfilling sponsors' study management activities and obligations in the EU region.

Key Responsibilities:
• Recruit, manage and lead FSP CTM staff across their respective region
• Ensure FSP staff are adequately trained and adhere to all appropriate SOPs, policies and applicable regulations and guidelines
• Ensure FSP staff achieve expected quality compliance standards with all appropriate SOPs, policies, regulations and guidelines
• Make study/site assignments in conjunction with sponsor's team
• Ensure FSP staff meet expected study timelines and deliverables
• Support FSP staff to achieve delivery of study objectives
• Provide regular feedback to sponsor management about operations of the FSP staff
• Evaluate performance metrics to identify process improvement areas
• Act as point of contact for sponsor
• Carry out performance management for staff not meeting appropriate sponsor expectations

Required experience and qualifications:
• BA/BS/BSc in the sciences or RN
• Previous experience in managing direct reports
• Experience working as a Study Manager/Project Manager (working on industry-sponsored or industry-partnered clinical trials or working on clinical trials at a biotech, pharmaceutical or CRO company).

How to apply?
This is an exceptional opportunity within a global organisation who offers rewarding careers. If you want to be a part of this exciting opportunity who offers a competitive salary, excellent benefits package, please contact Dariusz Sternlicht, Recruitment Consultant at DOCS and email your up-to-date CV to: dariusz.sternlicht@docsglobal.com

Benefits of working in ICON

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, 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.


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