Beschreibung

In this role, you will oversee clinical trial activities, ensuring compliance with protocols and regulations. Daily tasks will involve monitoring sites, conducting visits, and collaborating with teams to maintain data integrity and participant safety.

Anforderungen

• •Advanced degree in life sciences, nursing, or medicine
• •Extensive experience as a Clinical Research Associate
• •Strong understanding of clinical trial processes and regulatory requirements
• •Proven ability to manage multiple sites and projects
• •Strong organizational and problem-solving skills
• •Expertise in monitoring practices and data integrity
• •Proficiency in relevant clinical trial software and tools
• •Excellent communication and interpersonal skills
• •Stakeholder management skills
• •Ability to influence and drive compliance
• •Ability to travel at least 60% of the time
• •Possession of a valid driver’s license

Aufgaben

• •Monitor clinical trial sites for protocol adherence
• •Conduct site visits to assess performance and resolve issues
• •Collaborate with teams for accurate data collection and reporting
• •Provide training and guidance to site staff and CRAs
• •Build and maintain relationships with site personnel and stakeholders

Benefits