Clinical Research Associate (CRA)

SCIRENT Clinical Research and Science; Berlin; Vor Ort; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

An established industry player in clinical research is seeking a motivated Clinical Research Associate to join their dynamic team in Berlin. This exciting role involves coordinating study centers, ensuring compliance with clinical protocols, and leading stakeholder communications focused on groundbreaking cardiovascular research. You'll have the opportunity to contribute to the advancement of cardiovascular health while working in a modern office environment. The company values your professional development, offering in-house training and support for language courses. If you're passionate about making a difference in clinical research, this is the perfect opportunity for you.

Leistungen

Company pension scheme

In-house training

Voluntary language courses

Welcome trips to partner countries

Modern office in Berlin

Work equipment (laptop, telephone)

Qualifikationen

• Experience as a Clinical Research Associate is required.
• Familiarity with cardiovascular clinical trials is an advantage.

Aufgaben

• Coordinate study centers and ensure adherence to clinical protocols.
• Serve as the principal communicator between study site and stakeholders.
• Oversee documentation and reporting process for adverse events.

Kenntnisse

Leadership Skills

Organizational Skills

Communication Skills

Problem-Solving

Ausbildung

Bachelor’s degree in a clinical, scientific, or health-related field

Jobbeschreibung

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.

• 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

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.

SCIRENT Clinical Research and Science

Amrumer Str. 16, 13353 Berlin

Clinical Research Associate • Berlin Metropolitan Area, Germany