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Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded 1997, is a pan-European specialist staffing organisation with
offices in Munich, Basel and London, providing flexible resourcing solutions to the pharmaceutical
industry across Europe, with contract and permanent placements in clinical development, data
management, statistics, regulatory affairs and medical marketing
For our client, who belongs to the world’s most admired companies in the Health Care Pharmacy
industry, we are looking for a

Clinical Research Associate II (m/f)
Reference number:
Location:

893296
Munich or homebased

Responsibilities:
• Manage all aspects of site monitoring responsibilities for Clinical trials, according to Standard
Operating Procedures, ICH guidelines and GCP, including Pre-study qualification, Initiation
Meetings, Routine, Interim monitoring Visits and Close-out Visits

Requirements:
• Life Science Degree or certification in a related allied health profession from an appropriately
accredited institution (e.g., nursing licensure, medical or laboratory technology)
• Minimum of 1,5 years of relevant clinical research monitoring experience (including pre-study,
initiation, routine monitoring and closeout visits).
• Have a full understanding of Serious Adverse Event (SAE) reporting, process production of
reports, narratives and follow up of SAEs.
• Fluent in German and in English, both written and verbal
• Willingness to travel

Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to Rouven Scharun at rouven.scharun@ctcresourcing.com
CTC Resourcing Solutions, Landshuter Allee 8, 80637 München, Germany
Tel.: +49 89 54558337
Fax: +49 89 557443
www.ctcon.ch
info@ctcon.ch

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Clinical Research Associate / Senior Clinical Research Associate

  • 1. Providing Flexible Resourcing Solutions CTC Resourcing Solutions, founded 1997, is a pan-European specialist staffing organisation with offices in Munich, Basel and London, providing flexible resourcing solutions to the pharmaceutical industry across Europe, with contract and permanent placements in clinical development, data management, statistics, regulatory affairs and medical marketing For our client, who belongs to the world’s most admired companies in the Health Care Pharmacy industry, we are looking for a Clinical Research Associate II (m/f) Reference number: Location: 893296 Munich or homebased Responsibilities: • Manage all aspects of site monitoring responsibilities for Clinical trials, according to Standard Operating Procedures, ICH guidelines and GCP, including Pre-study qualification, Initiation Meetings, Routine, Interim monitoring Visits and Close-out Visits Requirements: • Life Science Degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology) • Minimum of 1,5 years of relevant clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. • Fluent in German and in English, both written and verbal • Willingness to travel Should you be interested in the above position and wish to apply, please send your application with your CV, quoting the above reference number, to Rouven Scharun at rouven.scharun@ctcresourcing.com CTC Resourcing Solutions, Landshuter Allee 8, 80637 München, Germany Tel.: +49 89 54558337 Fax: +49 89 557443 www.ctcon.ch info@ctcon.ch