Ref #: 31865

Employment type: Permanent - Full-Time

Location: Poland

Posted: 21-Sep-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.

Description:

* Ensure regional/global clinical operations deliverables progress according to agree upon timelines and milestones as leader of the Study Management Team (SMT). This includes country & site feasibility and site selection, trial set-up, study execution and trial closure and vendor set activities as assigned by the GTL. Support GTL in leading related CRO country & site activities.
•*Study Management Team Leader
•* Site selection, enrollment, monitor study progress
•* Financial planning and tracking
•* Document development
•* Training and Investigator Meeting
•* Cross functional Study Management
•* Continuous Quality Focus
•* Data Cleaning
•* Participate in Global Clinical Development Initiatives as assigned.
* Can act as Subject Matter Expert.

Profile:

* BS degree or equivalent required, preferably in Life Sciences (e.g., Biology,• Chemistry, Biochemistry, Nursing, Pharmacy)
*• Required: Minimum of 8 years clinical trial management experience in the pharmaceutical industry or CRO at least on local level
•* Experience with management and supervision of CROs/vendors is preferred.
* Clinical research operational knowledge, strong project planning/management and effective communication skills.
* Strong analytical skills, and simultaneously demonstrates the ability to manage ambiguity when limited information is available.
•* Effective verbal and written communication skills leading to successful team collaboration.
* Proven experience in proactive planning, risk mitigating and gaining team consensus on updated plans during the project lifecycle.
•* Willing to travel internationally up to 20% of time

Benefits of Working in ICON:
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. 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 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.