Senior Research Associate Role in Epilepsy Study
We are seeking a highly skilled and dedicated Senior Clinical Research Associate to support our Phase II/III Epilepsy Study in Brazil.
* The successful candidate will be responsible for managing multiple clinical sites, ensuring timely completion of study milestones and providing high-quality data collection.
* This is a contract role with an immediate start available, offering the opportunity to work on a challenging project with a talented team.
About the Opportunity:
This is a fantastic chance to join a leading research organization and contribute to advancing care for patients with seizure disorders.
Key Responsibilities:
* Study Management: Coordinate and manage all aspects of the study at assigned clinical sites, ensuring compliance with regulatory requirements and study protocols.
* Data Collection: Collect and compile accurate and complete data from study participants, maintaining high standards of quality and integrity.
* Clinical Site Support: Provide regular site visits, training and support to ensure successful implementation of the study protocol.
Requirements:
* Education: Bachelor's degree in a related field (e.g. life sciences, nursing, medicine).
* Experience: Minimum 3 years' experience in clinical research, preferably in a senior role.
* Skills: Strong knowledge of GCP, ICH and local regulations; excellent communication and interpersonal skills; ability to work independently and as part of a team.
Benefits:
This contract role offers a competitive remuneration package, including benefits and opportunities for professional growth and development.
Location:
The successful candidate will be based in Brazil, with frequent travel required to clinical sites.