Clinical Research Associate (CRA)

SCIRENT Clinical Research and Science is seeking a motivated Clinical Research Associate for a full‑time position in Germany, ideally based in Berlin or willing to relocate to Berlin. Candidates must be fluent in English and German. Proficiency in an additional language (Greek, Italian, or a Scandinavian language) would be advantageous.

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.

Your Profile

• Education: Bachelor’s degree or higher in a clinical, scientific, or health‑related field, ideally with a specialization in cardiology or cardiovascular medicine.
• Experience: Experience as a Clinical Research Associate is required. Familiarity with cardiovascular clinical trials is an advantage.
• Certifications: ICH/GCP trained, with additional qualifications in cardiovascular research preferred.
• Skills: Strong leadership and organizational skills, excellent communication abilities, and adept at problem‑solving within cardiovascular clinical settings.
• Language Proficiency: Fluent in English and German. Additional languages (Greek, Italian, or a Scandinavian language) are beneficial.
• Personal Traits: Proven ability to work both independently and as part of a team, committed to advancing cardiovascular health through rigorous clinical research.

Benefits

• Attractive salary and a company pension scheme.
• Onboarding program: welcome trips to partner countries, newcomers meet & greet to ensure a perfect start.
• Training: in‑house training in all areas of clinical research, voluntary language courses, and regular coaching.
• Work equipment: offices across Europe, laptop, telephone.
• Accessibility: modern office downtown Berlin, easy to reach.

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 enthusiasm for developing effective therapies for cardiac patients. What sets us apart from our competitors is 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 the lean and agile management that makes our performance faster and more efficient.

Application

We look forward to receiving your complete application documents, stating the possible start of work.

SCIRENT Clinical Research and Science
Amrumer Str. 16, 13353 Berlin