Clinical Research Associate
Há 7 dias
In the dynamic environment of IQVIA Argentina, we are seeking a Clinical Research Associate to join our Real World Evidence Department. As a key member of our team, you will support the management of clinical dossiers for clients across various industries.
Job DescriptionYour primary responsibilities will include:
- Supporting the health technology assessment (HTA) submission and reimbursement processes, including the preparation of Added Therapeutic Value dossiers and other clinical documentation.
- Conducting literature reviews and evidence synthesis to support clinical dossiers.
- Assisting in the preparation and submission of clinical trial applications and other regulatory documents.
- Collaborating with clinical teams to ensure the accuracy and completeness of clinical data.
- Contributing to the preparation, execution, and follow-up of client projects.
To be successful in this role, you will need:
- A degree in life sciences, pharmacy, nursing, or a related field.
- A postgraduate degree in clinical research, pharmacy, biostatistics, epidemiology, healthcare policy, or another healthcare-related discipline.
- A strong understanding of clinical research methodologies and of the Portuguese health care system.
- Previous work experience in clinical or outcomes research, real-world evidence, or evidence generation.
- Proficiency in Portuguese and English (both written and spoken).
- Strong communication skills.
- Excellent execution skills, consistently meeting deadlines.
- Keenness to learn and commitment to a rapid development curve.
- A self-driven approach and ability to work in a team.
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