Job Description
We are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and excellence in healthcare.
We value diversity and inclusion, fostering a collaborative work environment where all employees can contribute their ideas and talents. We believe that our strength lies in the people who are part of our team, and we are constantly looking for passionate and dedicated professionals who want to make a difference.
We are recruiting a Clinical Research Associate (CRA) to join our dynamic team in Portugal. This is a unique opportunity for professionals who wish to contribute to the execution of high-quality clinical studies and have a strong interest in driving innovation in the healthcare field. If you are looking for a stimulating and challenging environment where you can grow and develop your career, we are the right place for you.

EXPERIENCE AND EDUCATION:

• Bachelor’s degree in a health-related field, with at least 3 years of experience in clinical trial monitoring.
• Fluent in Portuguese and English (spoken and written), with excellent written and oral communication skills.

SKILLS AND QUALIFICATIONS:

• Solid knowledge of Good Clinical Practices and clinical trial monitoring.
• Experience in conducting clinical trials (validation visits, initiation, ongoing, and closure).
• Ability to manage complex scenarios, working solution-oriented.
• Good IT skills (MS Office) and knowledge of clinical trial management tools.
• Valid driving license.

REQUIRED SKILLS:

Accountability, Accountability, Adaptability, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Testing, Clinical Trial Planning, Clinical Trials Monitoring, Data Analysis, Data Reporting, Detail-Oriented, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Information Technology Applications, Intrapersonal Communication, Management Process, Microsoft Office, Monitoring Control, Portuguese Language, Proactive Approach, Problem Solving, Protocol Adherence, Regulatory Compliance {+ 3 more}

Please refer the Job description for details