Clinical Trials Manager, Burlington, MA

The Clinical Trials Manager is responsible for the delivery of a key phase 3 clinical trial. This individual will contribute to the success of the team and organization by delivering high quality operational excellence on all delegated responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and Enablement.

• Provide strategic and operational oversight for global clinical trials.
• Support CRO and vendor management, including governance, performance tracking, and risk mitigation.
• Collaborate with internal functions (Regulatory, Medical, Biometrics, Pharmacovigilance, CMC, quality) to align on study plans and timelines.
• Monitor trial progress against key deliverables (recruitment, data quality, protocol compliance, etc).
• Support country and site selection, start-up activities, and site engagement strategy.
• Manage and support sites in study maintenance for a fast-enrolling trial
• Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements.
• Support study budgets and contracts in collaboration with finance and legal teams.
• Contribute to clinical development strategy and operational planning.
• Prepare for and participate in study audits, inspections and data deliverables
• Attend Site Investigator Visits and build and maintain relationships with key stakeholders.
• Adhering to Company Standard Operating Procedures, Policies and applicable regulatory requirements
• Execute day-to-day responsibilities of the role, ensuring quality, accuracy, and timeliness.
• Collaborate effectively with colleagues, sharing knowledge and supporting team goals.
• Contribute to problem-solving and decision-making processes with an objective, data-driven approach.
• Communicate clearly and proactively with stakeholders to ensure alignment.
• Demonstrate ownership of tasks and follow through to successful completion.
• Support team members through constructive feedback, mentorship, and collaboration.

• Bachelor’s degree in life sciences, nursing, pharmacy, public health, or a related field (Advanced degree preferred but not required)
• ~7 years in Clinical Operations or related function
• Strong working knowledge of ICH-GCP, and experience working on global clinical trials
• Strong interpersonal and communication skills, with the ability to adapt to different audiences.
• Excellent organizational skills
• Proven ability to build trust and credibility through integrity, openness, and respect.
• Demonstrated accountability in delivering results and meeting commitments.
• Analytical mindset with the ability to use facts and data to guide decisions.
• Ability to work both independently and collaboratively within a team.

• Trust and Respect:
  Act with integrity, honesty, and openness to build strong, credible relationships.
• Communication and Feedback:
  Share information clearly, listen actively, and engage in a culture of constructive feedback.
• Accountability and Reliability:
  Take ownership for performance, be dependable, and support others to achieve collective goals.
• Objectivity:
  Align on common objectives and use facts and data to reach fair, effective decisions.
• Team Balance and Enablement:
  Contribute to balanced roles within the team, support delegation, and help colleagues reach their full potential.

At Cell Centric, we believe success is built on great teams. By embodying these working behaviors, every member contributes to a high-performing, supportive, and inclusive culture where individuals and the business thrive together.