Sr clinical research analyst – Campinas/SP

Efetivo (CLT)

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.

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).