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Job Opportunity

5 July 2018

For the last quarter 2018 we are looking for dedicated, enthusiastic and motivated employees, home office based from the Rhine-Main area Germany, Manchester, England and Guernsey,Channel Islands that will join the SynapCon team as:

Clinical Research Associate (f/m)


•    Responsibilities for the organization, coordination, administrative management and monitoring of clinical trials        (phase I – IV) according to ICH/GCP guidelines
•    Interact directly with clinical sites, including clinical investigators and other health care professionals                     involved in the clinical study and maintain a positive relationship with each site
•    Data review and source data verification
•    Ensure investigator compliance with protocol, study procedures and timelines
•    Conducting source data verification and in-house review of clinical data and ensuring timely resolution of data queries


•    Medical or scientific education (medicine, nursing, pharmacy, biology, biomedical sciences or equivalent)
•    Minimum three years of experience as CRA including monitoring experience in Germany
•    Strong knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
•    Fluent German and English language skills
•    Excellent interpersonal and communication skills, independent and efficient working methods
•    Willingness to travel (driver's license)
•    Applications of contractors/freelance CRA's are welcome

SynapCon Ltd. offers

•    Dynamic working environment, large diversity in working assignments
•    A market conform salary adjusted to your qualifications and experience
•    Coaching and training system

Are you interested? Please send your application via email to:

SynapCon Limited
Office Germany
POB 13 02 50
65090 Wiesbaden
Phone: +49 (0) 611 70397054
Fax: +49 (0) 611 71029495

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For detailed information please contact us:

phone: +49 (0)611 70397054
mail: info@synapcon.com