Clinical Research Associate (CRA)

SCIRENT Clinical Research and Science; Santiago de Compostela; A distancia; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading company in clinical research is seeking a motivated Clinical Research Associate for a full-time position in Spain. This role offers the opportunity to coordinate cardiovascular studies, ensure compliance, and train personnel. Candidates should be fluent in English and Spanish, with relevant educational qualifications and experience in clinical research.

Servicios

Attractive salary

Company pension scheme

In-house training in clinical research

Voluntary language courses

Welcome trips to partner countries

Formación

• Experience as a Clinical Research Associate required.
• Familiarity with cardiovascular clinical trials is an advantage.
• ICH/GCP trained, additional qualifications in cardiovascular research preferred.

Responsabilidades

• Coordinate study centers to ensure adherence to clinical protocols.
• Train study personnel on specific protocols.
• Oversee documentation and reporting processes.

Conocimientos

Leadership

Organizational skills

Communication

Problem-solving

Educación

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

Descripción del empleo

SCIRENT Clinical Research and Science is seeking a motivated Clinical Research Associate for a full-time position in Spain. We are accepting applications from candidates across the country. The role requires a willingness to travel nationally.

Candidates must be fluent in English and Spanish at an academic level. Proficiency in an additional language (Greek, Italian, or a Scandinavian language) would be considered an advantage.

Area of Responsibility

Site Management: Coordinate study centers to ensure 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 Spanish. 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: Remote work within Spain is possible with national travel requirements.

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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

www.scirent.com