Sr clinical research analyst – Campinas/SP

SP l São Paulo
Efetivo (CLT)
Biólogo
Médico Veterinário
Zootecnista

Responsabilidades

• Assistance to all study activities, including start up, investigator training, study conduct, site monitoring and close out.
• These may include, but are not limited to: CRO selection and training.
• To ensure the execution of clinical studies in compliance with good clinical practices, animal welfare and applied legislation.
• Assisting in preparation of study protocols, data capture forms, electronic data capture, test article documentation and study reports.
• Maintaining study files in accordance with Standard Operating Procedures (SOPs) and regulatory requirements.
• Assisting in data management processes including data review, tracking and verification.
• Serve as a communication link between the sponsor and study site, including study site monitoring activities which require ability to travel regularly and independently (short periods of 1-3 days).
• Provide support for the elaboration/review of quality assurance clinical documents.
• Provide support to departmental colleagues.
• Collectively responsible for the timely deliverables of new products in Brazil.
• He/she will interact with other VMRD colleagues (locally and globally) such as Project Team Leaders, Biometricians, Data Managers and other areas as Regulatory Affairs and Commercial.

Requisitos

• Degree in Veterinary Medicine or other relevant biological field (e.g. biology, animal science, etc).
• A MSc and/or PhD could be an advantage.
• Solid experience with veterinary clinical research studies.
• Demonstrate good inter-personal communication and presentation skills as this position will interact with other teams and all level of management.
• Good written and oral command of Portuguese and English language (A strong ability in scientific writing could be an advantage).
• Availability to travel (short periods of 1-3 days) and holds a driver license (category B).