SCIRENT Clinical Research and Science is seeking a motivated Clinical Research Associate (CRA) for a full-time position in Germany, ideally based in Berlin or willing to relocate to Berlin.
Fluency in German and English at a minimum C1 level is required.
In addition, at least one year of documented on-site monitoring experience as a CRA is mandatory.
Alternatively, we also consider Study Coordinators or Study Nurses with at least one year of experience in clinical trials, either on the sponsor side or at the site level.
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Area of Responsibility
Site Management: Coordinate study centers, ensuring adherence to clinical protocols and regulatory standards, with a focus on cardiovascular research.
Team Leadership and Training: Train study personnel at centers on the specific protocols.
Stakeholder Communication: Serve as the principal communicator between the study site and stakeholders, focusing discussions around cardiovascular study objectives.
Audit Preparation and Compliance: Ensure that cardiovascular study sites are prepared for audits and maintain strict compliance with specific regulatory requirements.
Clinical Documentation: Oversee the documentation and reporting process, ensuring accurate and timely follow-up of adverse events and serious adverse events related to cardiovascular issues.
Regulatory Support: Assist with regulatory filings and communications, specifically related to cardiovascular studies, maintaining compliance with local and international guidelines.
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Your Profile
Education: Bachelor’s degree or equivalent qualification in life sciences, nursing, medicine, or a related health/scientific field.
Experience: A minimum of one year of hands-on experience in clinical research is required. This includes either documented on-site monitoring experience as a Clinical Research Associate (CRA) or at least one year of experience as a Study Coordinator or Study Nurse involved in the conduct of clinical trials at sponsor or site level.
Certifications: ICH/GCP trained, with additional qualifications in cardiovascular research preferred.
Skills: Strong interpersonal and communication skills, with the ability to work effectively in team-oriented and flat organizational structures. Comfortable navigating the hospital environment and maintaining professional, respectful relationships with investigators, study staff, and clinical personnel. Adaptable, collaborative, and solution-oriented in day-to-day clinical settings.
Language Proficiency: Fluent in English and German. Additional languages (Greek, Italian, or a Scandinavian language) are beneficial.
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-more-
Extra: attractive salary and a company pension scheme
Onboarding: Welcome trips to our partner countries, newcomers meet & greet - we ensure your perfect start
Training: Your development is important to us. We offer in-house training in all areas of clinical research. There is the possibility of voluntary language courses or regular coaching - we will keep you up to date!
Work equipment: We offer offices all over Europe, a laptop, telephone.
Accessibility: Our modern office right in the heart of Berlin is easy to reach thanks to its perfect location
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About us
SCIRENT was founded in 2012 with the vision of helping customers develop innovative medical drugs and devices for patients with cardiovascular diseases. Our dedicated team of experienced clinical and regulatory professionals share their enthusiasm for developing effective therapies for cardiac patients. What sets us apart from our competitors is our profound expertise in cardiovascular therapy and diagnostics. Our CRO offers access to an impeccable network of dedicated trial centers in Europe and North America with extensive experience in cardiovascular studies. Our customers appreciate our lean and agile management, which generally makes our performance faster and more efficient.
We are looking forward to receiving your complete application documents, stating the possible start of work.
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CEO: Prof. Dr. med. Hans-Dirk Düngen
SCIRENT Clinical Research and Science
Amrumer Str. 16, 13353 Berlin