Trial Delivery Manager, Multi TA

Jobtailor; Massachusetts; On-site; USD 90,000 - 130,000; Full time

Job summary

Jobtailor in the United States is seeking an experienced Clinical Trial Manager to lead and coordinate global and regional trials, ensuring quality and compliance across the full lifecycle from feasibility to close-out.

You will be the primary contact for country, regional, and functional stakeholders, drive site selection and startup, oversee documentation and inspection readiness, and mentor junior team members. English fluency is required and travel is anticipated.

Qualifications

• Bachelor’s degree in Life Sciences required.
• 6+ years of clinical trial management experience in pharma/CRO.
• Experience leading trials from startup to close-out.
• Fluent in English; local language proficiency as required.

Responsibilities

• Lead and coordinate global and regional clinical trial management activities.
• Act as primary point of contact for country, regional, and functional stakeholders.
• Drive trial delivery across the full lifecycle: feasibility, site selection, start-up, execution, and close-out.
• Ensure continuous inspection readiness in accordance with ICH-GCP.
• Oversee trial documentation, filing, archiving, and retention.
• Provide coaching and mentoring to less experienced team members.

Skills

Project management

Risk mitigation

Cross-functional coordination

Education

Bachelor’s degree in Life Sciences

Tools

CTMS

TMF systems

Microsoft Office

Job description

Responsibilities

• Lead and coordinate global and regional clinical trial management activities
• Act as primary point of contact for country, regional, and functional stakeholders
• Drive trial delivery across the full lifecycle: feasibility, site selection, start-up, execution, and close-out
• Ensure continuous inspection readiness in accordance with ICH-GCP
• Oversee trial documentation, filing, archiving, and retention
• Provide coaching and mentoring to less experienced team members

Requirements

• Bachelor’s degree (or equivalent) in Life Sciences
• 6+ years of clinical trial management experience in pharma and/or CRO environments
• Proven experience managing trials from start-up through database lock and close-out
• Strong project management, planning, and risk mitigation skills
• Experience with CTMS, TMF systems, and Microsoft applications
• Fluent in English; local language proficiency as required
• Willingness to travel as needed.