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Site Identification Specialist - (Polish Speaker)

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About the role

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Do you have experience building relationships with study investigators/sites and networks for the conduct of feasibility and site ID?

 
Site ID Specialist role within ICON: 
 

ICON has a strong reputation in our approaches to clinical development.   We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients.   We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain.  We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. 

 

The Site ID Specialist will work with the Site ID Lead to ensure knowledge of the goals, scope and requirements of the site ID project (e.g. number of sites required/country, number of positive responses required etc.) and ensure that high quality results are delivered. Identify study investigators/ sites for potential study participation, both from the database and other potential sources such as local intelligence/internet etc.

 

Ensure all newly identified sites are data based appropriately, checked for quality status and are fully processed. 

Ensure that all data collected in the conduct of site identification or site related country feasibility fully documented and kept up to date in ICON’s systems in order to build knowledge and intelligence.  To contact investigators, local ICON employees and collect data to support country choice in the conduct of feasibility assessments.

To become a country expert on the investigator profile, healthcare setting, standard of care to ensure the best sites are approached for projects. Be an expert on how to interact with sites and obtain relevant information to support feasibility and site identification and use knowledge and experience to build efficiency in the process and consistently deliver high quality investigators, sites, and other data to the Functional Lead for your feasibility projects.


Requirements

To succeed you will need a Bachelor’s degree, or local equivalent, in a life science, communication, and/or scientific discipline. 

 

We are seeking candidates with 2 or more years of experience, in a health care or a clinical research environment.  Intermediate skills in MS Word, Excel and PowerPoint, advanced skills are preferred, particularly for Excel.  Highly developed organizational and analytical skills, with the ability to prioritize time-sensitive tasks and work independently.  

The ability to speak fluent Polish and English is a must.

 
 
Benefits of working at ICON:
 

In addition to partnering with the top pharmaceutical and biotech companies in the world we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives.  

 
 
 
What’s Next?
 

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

 

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

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