Clinical Research Associate

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.

• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.

• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What You Will Be Doing

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.