CRA / Medical Monitor – German speaking – UK based –Circa- £45,000
CRA / Medical Monitor – German speaking – UK based –Circa- £45,000 Brief overview of role/opportunity We are currently looking for an experienced CRA who enjoys working on study start up ( ethic submissions) through to close out to join our highly productive and quality focussed clinical operations team. We are a unique BIOPHARMA working in a highly complex therapy areas, if you want to work within a setting where your work truly matters and its less about the numbers, then we want to hear from you! Ideally, we are looking for a talented individual with strong previous experience in monitoring, ethics submissions and start up, with excellent communication skills, the ability to speak fluent German and someone who truly cares about the quality and outcome of the trials. However if you do not have start-up experience but would like to learn then we are more than happy to hear from you! Please contact Zoe Benningfield-Fox on 0203 019 6022 or email email@example.com if you would like to know more about this opportunity. This will be 100% confidential. COMPANY BACKGROUND: We are a unique BIOPHARMA based in the home counties working within highly specialised therapeutic area. Our work truly makes a difference to thousands of people both in the UK and worldwide so we need a CRA / SCRA/ Medical Monitor who takes pride in their work and always has the patient population in mind. Please contact Zoe Benningfield-Fox on 0203 019 6022 or email firstname.lastname@example.org if you would like to know more about this opportunity. This will be 100% confidential. ROLE RESPONSIBILITIES Performs and coordinate all aspects of the clinical monitoring and site management Conducts site visits - assessing protocol and regulatory compliance, managing required documentation Develops and maintaining collaborative relationships with investigational sites and client company personnel. Leading on assigned clinical studies Mentor, train and contribute to the development of junior clinical SKILLS DESIRED Ideally 18 months plus monitoring experience Ethics submissions and study start up Advanced ICH-GCP knowledge Ability to mentor and co-monitor with junior CRAs Effective written and verbal communication skills Meet is a European wide recruitment agency who specialise purely in the pharmaceutical sector. We work in a number of regions across Europe placing both permanent and freelance candidates into Clinical, Regulatory and Data management teams within CRO’s, Pharmaceutical, Generic and Biotech companies. KEY WORDS CRA, Clinical Research Associate, Clinical Monitoring Associate, Clinical Monitor, CRO, SCRA, Senior clinical research associate, LCRA, lead clinical research associate, early phase, late phase, study start-up, study initiation, routine monitoring, study close out, clinical site management, ICH-GCP, co-monitoring.