Ref #: 32260

Employment type: Permanent - Full-Time

Location: Poland

Posted: 19-Oct-2021

Description

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance.
We are hiring a Clinical Research Associates and Senior CRAs to work closely with our client, a leading pharmaceutical company.

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.


Overview:
In this role you will act as a ‘face’ of the sponsor, provide an interface between the sponsor company, the investigator and the vendor in outsourced trials. You will develop and maintain long-term relationships with clinical investigators, enhancing the image and reputation of the company. You will be responsible for providing operational expertise to sites through ownership and management of clinical site strategy.

This is a field based role that requires frequent business trips across Poland up to 50%.


Required experience and qualifications:
Previous site oversight and relationship building experience (Investigators, KOLs, sites, CROs, vendors, etc)
Previous Sr CRA/CTM experience plus some sales or medical background would be an advantage
Strong experience in a clinical project management field within the Pharmaceutical or CRO industry
Experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required
Very good spoken and written English

Key Responsibilities:
Responsible for building and managing site relationships while overseeing site-level study start-up, conduct, and close-out activities
Assist sites with enrolment barriers by reinforcing protocol specific site recruitment plans. Define and implement strategies for engaging clinical sites and investigators
Independently perform activities associated with the evaluation of investigational sites in order to build company network
Single point of contact for institutions to resolve business process barriers.
Act as liaison between the company and investigational sites building investigator and site staff awareness on sponsor company
Evaluate, screen and develop high quality investigative sites to support sponsor’s clinical development programs.


How to apply?
Please email your up-to-date CV to: dariusz.sternlicht@docsglobal.com

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, 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.


#pmjob