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Clinical Research Patient Recruiter (Europe)

Position Summary:
The Clinical Research Patient Recruiter (Europe) will manage overall clinical trial patient recruitment activities for our enrolling clinical studies in Europe. Working in conjunction with the internal and external clinical teams and any active clinical marketing programs drive local site recruitment by developing strong working relationships with clinical center recruitment teams/offices/departments and support all aspects of tailored local recruitment activities. The position will also be responsible for communicating internally any market dynamics, study issues or potential improvements.  Any recruitment downtime will be filled with productive clinical activities as assigned by supervisor and may include items such as site management, monitoring or device support.
 
Responsibilities:
The primary objective of the Clinical Research Patient Recruiter (CRPR) is to create and utilize proper tools, processes, and training that enable us to develop effective strategies and tactics for subject referrals, recruitment and retention in our active clinical trials.  The position will be responsible for executing some or all of approved clinical marketing activities, if appropriate, and proactively identifying project challenges, problems, and/or potential efficiencies in patient recruitment and communicating these appropriately to Study Manager.  The CRPR will keep abreast of SOPs, related EU Good Clinical Practice (GCP) and ICH guidelines, regional and national laws and ethical standards. Position must be able to read and understand scientific Investigational Brochures, protocols, consent forms, etc., for a thorough understanding of the study device and protocol requirements.  The CRPR will work professionally with colleagues to achieve other departmental goals as delegated.
 
Qualifications:
  • An undergraduate degree in a related field is essential with 3+ years of direct experience with investigational study activities and medical devices
  • Proven organization skills and the ability to manage multiple priorities
  • Excellent communication, both oral and written, and presentation skills
  • Strong interpersonal skills
  • Strong computer skills (Microsoft Office Suite)
  • Ability to effectively solve problems
  • Ability to work independently (field based position)
  • Ability to travel up to 80%. Limited Non-EU travel may be required
  • Familiarity with pulmonary clinical research preferred
 
 
This job description is intended as a summary of the primary responsibilities of and qualifications for this position. The job description is not intended as inclusive of all duties an individual in this position might be asked to perform or of all qualifications that may be required either now or in the future.
 
 

Contact detail


How to apply:
Please email your CV/Resume and Cover Letter to hr@holaira.com .  Be sure to include the reference number 102CRPR.
Send application to
hr@holaira.com

Job profile


Working hours
Full-Time
Contract duration
Permanent
Type of job
Specialist
Region
Germany
Working place
60388 Europe (preferred Central EU), close to major demo center (Frankfurt, Paris, London).
Area of expertise
Healthcare & Public Health, Biology & Life Sciences, Medical Engineering
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