Senior Clinical Research Analyst | Campinas (SP)

Zoetis; Campinas; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A global leader in animal health is seeking a dedicated professional in Campinas, São Paulo to coordinate veterinary clinical studies. The role involves supporting research and development projects while ensuring compliance with regulatory standards. Candidates should hold a degree in Veterinary Medicine or a relevant biological field, along with solid experience in clinical research. Fluency in Portuguese and English is required, and candidates must be willing to travel nationally for short periods. This is a full-time position offering a dynamic work environment.

Qualificações

• Degree in Veterinary Medicine or similar field required.
• MSc and/or PhD is an advantage.
• Solid experience in veterinary clinical research studies is essential.
• Strong communication and presentation skills required.
• Fluency in Portuguese and English is mandatory.

Responsabilidades

• Coordinate and track clinical studies for biological projects.
• Assist in all study activities including site monitoring.
• Support the preparation of study-related documents.
• Maintain study compliance with regulatory requirements.
• Act as a communication link between sponsor and study site.

Conhecimentos

Veterinary clinical research

Interpersonal communication

Scientific writing

Presentation skills

English language proficiency

Portuguese language proficiency

Formação académica

Degree in Veterinary Medicine or relevant biological field

MSc and/or PhD

Descrição da oferta de emprego

Zoetis values and supports inclusion, upholding equal opportunities.

Location: Campinas (SP)

Role Description

Responsible for coordinating and tracking, with coaching and support, research & development clinical studies for biologicals projects in compliance with appropriate regulatory requirements and internal policies. Effectively collaborates with the cross‑functional development team (regional research and development team VMRD‑Brazil) to support new products licensing in Brazil and Latin America. The position is based in Campinas – São Paulo with frequent interactions with colleagues and external partners located around Brazil, requiring availability to travel.

Responsibilities

1. 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.
   • Ensuring the execution of clinical studies in compliance with good clinical practices, animal welfare and applicable 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.
   • Serving 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).
2. Providing support for the elaboration/review of quality assurance clinical documents.
3. Providing support to departmental colleagues.
4. 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 such as Regulatory Affairs and Commercial.

Requirements

• 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 levels 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 licence (category B).

Full time