Senior Global Trial Manager

Senior Global Trial Manager

Requirements

• Bachelor’s Degree in health care or other scientific discipline.
• 7 years of clinical research/monitoring experience or an equivalent combination of education, training, and experience.
• Consolidated knowledge of project management practices and terminology.
• Good knowledge of applicable clinical research regulatory requirements (GCP, ICH guidelines).
• Other Equivalent combination of education, training, and experience may be accepted in lieu of degree.

Responsibilities

• Ensuring clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs.
• Meeting project recruitment targets and develop appropriate recruitment strategies.
• Contributing to project risk mitigation plans and manage clinical risks throughout the project lifecycle.
• Ensuring clinical quality delivery by identifying quality standards, planning compliance measures, and managing clinical quality issues.
• Managing clinical aspects of project finances, including Estimate at Completion (EAC), and identify additional service opportunities.
• Leading clinical teams to deliver large, global trials and manage internal and external stakeholders.
• Supporting milestone achievements and reporting to stakeholders as per project scope requirements.
• Managing the clinical team at the project level, including resourcing, talent planning, and providing project-related training.

Preferred Qualifications

• Strong written and verbal communication skills, including good command of the English language.
• Problem-solving skills and the ability to handle conflicting priorities.
• Attention to detail and accuracy in work, with a results-oriented approach.
• Good influencing, negotiation, judgment, and decision-making skills, with effective mentoring and training abilities.