Single Sponsor European Clinical Trial Manager

Single Sponsor European Clinical Trial Manager

Updated: Yesterday Location: London, POST-LON, United Kingdom Job ID:

Description

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators to navigate complexity, anticipate change, and accelerate progress across the drug development continuum.

Why Work With Syneos Health

• We are passionate about developing our people, providing career development, progressive line management, technical training, peer recognition, and total rewards.
• We are committed to building an inclusive culture with authenticity, driven by our purpose "Driven to Deliver".
• We strive to build the company we all want to work for and help shape the future of healthcare.

Job Responsibilities

• Office presence: 2-3 days a week in Uxbridge, moving to Central London Q2 2027.
• Therapeutic area: CAR T cell therapy, oncology - Multiple Myeloma.
• Coordinate Phase III clinical research studies across Europe, ensuring meticulous planning and execution.
• Participate in and manage project meetings and conference calls with CROs, vendors, and multi functional teams.
• Anticipate obstacles and proactively develop solutions to achieve project goals.
• Participate in abstract presentations, oral presentations and manuscript development activities.
• Interact and cooperate with individuals in other functional areas to address routine study issues.
• Assist in training Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).
• Assist in selecting CROs or vendors and coordinate their activities.
• Maintain study timelines and ensure adherence to global and regional regulations and guidelines.

Qualifications

• Bachelor's degree in life sciences, clinical research, or related field.
• Experience managing regional studies across European regions.
• In depth knowledge of clinical research processes and regulations from CRO or Pharma background.
• CRO oversight experience.
• Strong project management and organizational skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency with clinical trial management software and tools.

Necessary Skills

• Strong analytical and problem solving skills.
• Attention to detail and accuracy.
• Ability to manage multiple projects and priorities simultaneously.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

Additional Information

Tasks, duties, and responsibilities are not exhaustive and may evolve. Equivalent experience may be considered. The Company complies with the applicable laws of each country in which it operates, including the EU Equality Directive. The Company is committed to compliance with the Americans with Disabilities Act and offers reasonable accommodations when appropriate.

Summary

As a P22 level Clinical Trial Manager, you will oversee the development, coordination, and implementation of Phase I IV studies, ensuring milestones, budgets, and regulatory compliance while collaborating with principal investigators and cross functional stakeholders.

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