Clinical Study Lead/Global Trial Manager - Remote

Overview

Join Parexel as a Clinical Study Lead responsible for the global execution of clinical trials, ensuring that each phase from study design to closeout is managed effectively.

In Short

• Lead cross-functional study teams for clinical study delivery.
• Provide operational input into protocol development.
• Oversee development of study-specific documentation.
• Manage study systems including CTMS and TMF.
• Ensure compliance with clinical trial registry requirements.
• Identify and manage outsourcing needs and vendor engagement.
• Contribute to baseline budget development and management.
• Work with a focus on patient well-being.
• Collaborate with a vast client base across therapeutic areas.
• Utilize technical proficiency in trial management systems and MS applications.

Requirements

• Bachelor’s degree and a minimum of 6 years in global trial management.
• Technical proficiency in trial management systems and MS applications.
• Knowledge of ICH GCP and relevant regulatory guidelines.
• Demonstrated interpersonal and leadership skills.
• Strong communication skills in verbal, written, and presentation formats.
• Ability to implement strategic direction for clinical studies.

Benefits

• Opportunity to impact patient well-being positively.
• Work with a global team of over 16,000 employees.
• Comprehensive drug development capabilities.
• Engagement with a diverse client base.
• Access to advanced commercialization services.