Senior Local Trial Manager (Remote) (Canada) (Clinical)

About the role

As a Senior Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

What Will You Be Doing

Working outsourced and fully dedicated to one of our global pharmaceutical clients, the Senior Local Trial Manager is responsible for the successful management and execution of study activities at a country level. Collaborating with the wider global study team, the Local Trial Manager leads the local team of Site Managers and Clinical Trial Assistants in order to deliver quality data and trial documents that are compliant with protocol, ICH-GCP guidelines, Standard Operating Procedures and regulatory requirements.

Key Tasks Include (But Not Limited To):

• Development of local study tools and procedures
• Targeted and effective study team training
• Accompanying Site Managers on on-site visits to ensure protocol compliance at a site level, and to foster positive working relationships with site staff, including Investigators
• Preparation for audits
• Managing the local team to meet recruitment targets
• Managing studies from feasibility through to database lock and close-out, the Local Trial Manager acts as the key local manager throughout the lifecycle of the project
• Proactive risk management and budget forecasting
• Timely review of trip reports submitted by Site Managers
• Some on-site monitoring of assigned sites
• The efficient management of local vendors

What Do You Need to Have:

• Good written and oral communication skills.
• Flexible mindset and ability to work at a fast pace within small exploratory study teams.
• Solid understanding of the drug development process including ICH/GCP and local regulatory requirements.
• Willingness to travel with occasional overnight stay away from home depending on the region.
• Advanced: 3 to 5+ years of trial management experience.
• Solid communication and computer skills required.
• A minimum of a 4-year Bachelor’s degree or relevant clinical experience is required
• To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.
• Ability to work on multiple trials in parallel in different disease areas.
• Proficient in speaking and writing the country language and English language.
• At least 2 years of Oncology experience required