Career at AKP

Clinical Research Associate (m/f, office based)
The CRA will be responsible for conduction clinical trials of phases I-IV, NIS and
medical device studies. The key responsibilities will include:

• Site selection and feasibility
• Conduction of pre-site visits, study initiation, interim monitoring and close-out visits in
  accordance with regulations and SOPs
• Develop, review and edit clinical trial related documentation (CRFs, ICFs, study specific
  handbooks, guidelines, checklists)
• Manage clinical trial documentation including the TMF
• Preparation and coordination of Investigator’s Meetings
• Ethic submissions
• Manage Serious Adverse Event (SAE) reports


Skills required:
• Min. 1-2 years of monitoring experience
• Good knowledge of ICH-GCP, monitoring procedures and understanding of the clinical trial process
• Fluent English, spoken and written
• Willingness and ability to travel (ca. 50%)
• Excellent communication and interpersonal skills
• Advanced computer skills
• Flexibility, ability to work independently to coordinate all necessary activities required to set up and
  monitor a study


We offer:
• A competitive salary
• Permanent employment
• Active participation in the design and conduct of clinical projects
• Managing the whole project from the start to the end
• Extensive subject-specific trainings
• Regular in-house coaching
• A beautiful city in an attractive area of Southern Germany near Switzerland and France


We are looking forward to hearing from you! Please send your electronic application to:

Hilde Huber, Email: h.huber@akp-freiburg.de

Arbeitskreis Klinische Prüfungen
PD Dr. med. Seiler GmbH
Munzinger Str. 10
79111 Freiburg/Germany

phone:+49 761 479 40-0
fax:+49 761 479 40-22
mail: info@akp-freiburg.de