We are looking for a talented and highly motivated Clinical Research Associate (CRA) to join Roche’s clinical research team. In this role, you will be responsible for ensuring that all clinical activities are conducted in accordance with the company’s policies and procedures, as well as any applicable regulatory requirements. This is a great opportunity for someone who is passionate about clinical research and is looking to make an impact in the field.To be successful in this position, you must have a bachelor’s degree in a health-related field, such as nursing, pharmacy, or a related field. You should also have at least three years of experience in clinical research or a related field. Additionally, you must be proficient in the use of clinical trial management systems. A strong background in GCP and ICH guidelines, as well as knowledge of relevant regulations and guidelines, is also preferred.We are looking for a self-starter who is able to work independently and take initiative. The ideal candidate should have excellent communication and organizational skills, as well as the ability to work in a fast-paced and highly demanding environment. A positive attitude and a commitment to the highest standards of quality and integrity are also essential. If this describes you, we would love to hear from you!
Responsibilities:
- Ensure clinical activities are conducted in accordance with company policies and procedures, as well as applicable regulatory requirements.
- Provide support to the clinical research team in the implementation of clinical trials.
- Assist in the development of clinical trial protocols and Investigator Brochures.
- Monitor clinical trial sites to ensure compliance with Good Clinical Practice (GCP) and ICH guidelines.
- Maintain accurate records of all clinical activities.
- Analyze clinical data and generate reports.
- Develop and implement processes to ensure protocol and regulatory compliance.
- Liaise with stakeholders, such as investigators, sponsors, and other personnel, to ensure clinical trials are conducted according to protocols.
- Provide training to clinical research staff on GCP and ICH regulations.
- Ensure the timely submission of clinical trial documents.
Ability To Work Independently And Collaboratively
Excellent Communication And Interpersonal Skills
Biostatistics
Proficiency In Data Analysis And Interpretation
Good Organizational Skills
Proficiency With Microsoft Office And Other Software Programs
Ability To Multitask And Prioritize Competing Tasks
Knowledge Of Clinical Research Regulations And Guidelines
Bachelor's Degree In A Relevant Field (Eg.
Health Sciences
Epidemiology)
Documentation
Quality Assurance
Process Improvement
Project Management
Data Analysis
Communication
Problem Solving
Report Writing
Risk assessment
Teamwork
Regulatory compliance
Site management
Monitoring
Clinical Trials
Protocol Development
Communication
Leadership
Time management
Interpersonal Skills
creativity
Organization
Critical thinking
collaboration
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Associate in Madrid, Spain is €28,000 to €50,000 per year. This range can vary depending on a variety of factors such as experience and qualifications.
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Roche Holding AG operates as a research healthcare company. It operates through the diagnostics and pharmaceuticals segments. The pharmaceutical segment refers to development of medicines in the field of oncology, immunology, ophthalmology, infectious diseases and neuroscience. The diagnostic segment refers to diagnosis of diseases through an in vitro diagnostics process.

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