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About the Role
The Senior Manager, Clinical Operations is responsible for the operational planning, execution, and oversight of clinical trials supporting the company’s clinical development programs. This role may serve as the Lead Clinical Trial Manager or function as a key operational contributor within a larger program team. The position ensures clinical trials are conducted in compliance with applicable regulatory requirements, ICH-GCP guidelines, company Standard Operating Procedures (SOPs), and study protocol. The Senior Manager collaborates cross-functionally with internal and external stakeholders and external service providers to ensure the successful delivery of clinical trials with respect to quality, timelines, and budget. The Senior Manager may have direct reports, and will provide leadership, mentorship, and operational guidance to junior team members. The Senior Manager, Clinical Operations supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
Responsibilities
- Lead or support the operational execution of Phase I-IV clinical trials.
- Serve as Lead Clinical Trial Manager for assigned studies, with responsibility for study timelines, operational strategy, and study deliverables.
- Contribute to the development planning and operational feasibility assessments.
- Develop and manage key study documents including Clinical Trial Management Plans, study timelines and milestone tracking, and vendor scopes of work and operational budgets.
- Oversee study start-up, conduct, and close-out activities.
- Provide operational oversight of Clinical CROs and other operational service providers to ensure delivery of services consistent with contracted agreements and study requirements.
- Participate in service provider selection, RFP development, and contract review.
- Monitor service provider performance, study metrics, and key performance indicators to ensure study quality and timelines are maintained.
- Partner with internal functions including Clinical Development, Data Management, Biostatistics, Regulatory Affairs, Medical Writing, Project Management, Clinical Supply, and Quality Assurance.
- Ensure alignment of operational study and overall program strategy and development timelines.
- Ensure clinical trials are conducted in accordance with ICH-GCP guidelines, applicable global regulatory requirements, and company policies and standard operating procedures.
- Support inspection readiness and contribute to audit preparations and follow-up activities.
- Identify operational risks and develop mitigation and contingency strategies.
- Provide oversight of site identification, feasibility, selection, and activation activities.
- Review monitoring reports and key study metrics to ensure appropriate study oversight.
- Support resolution of site issues, enrollment challenges, and protocol implementation questions.
- Contribute to study budget development and ongoing financial oversight.
- Monitor study progress against timelines, key milestones, and performance metrics.
- Identify potential risks to study execution and implement corrective actions as needed.
- Manage and develop direct reports.
- Provide mentorship, guidance, and oversight of junior Clinical Operations staff.
- Support performance management, professional development, and training of team members.
- Foster a collaborative and high-performing clinical operations team environment.
- Contribute to preparation of study management plans, service provider oversight documentation, and operational reports.
- Provide regular updates on study status, risks, and mitigation strategies to Clinical Operations Leadership.
- Ensure study documentation is maintained in accordance with company requirements and is inspection ready.
- Perform other tasks and assignments as needed and specified by management.
Requirements
- Bachelor’s degree in a scientific discipline and a minimum of 7 years of progressively responsible US and/or global experience in clinical research in a pharmaceutical, biotechnology, CRO or related environment OR equivalent education and/or experience.
- Strong knowledge of ICH-GCP guidelines and global clinical trial regulations.
- Demonstrated ability to lead clinical trial operations and cross-functional teams.
- Demonstrated leadership ability and experience managing, coaching and mentoring direct reports (if managing people).
- Strong project management and organizational skills.
- Experience with risk-based quality management and vendor oversight models.
- Analytical thinker with excellent communication, collaboration, and problem-solving abilities.
- Ability to balance strategic oversight with operational execution.
- Passion in advancing therapies for patients with unmet medical need.
- Experience with Microsoft Office Suite.
Skills
- ICH-GCP guidelines
- Global clinical trial regulations
- Clinical trial operations leadership
- Cross-functional team leadership
- Managing, coaching, and mentoring direct reports
- Project management
- Organizational skills
- Risk-based quality management
- Vendor oversight
- Analytical thinking
- Communication
- Collaboration
- Problem-solving
- Strategic oversight
- Operational execution
- Microsoft Office Suite
- Executing clinical trials in rare disease populations
- Working with global centers of excellence and highly specialized investigative sites
- Strategic CRO partnership models
- Formal service provider oversight documentation
- Risk-based quality management frameworks
- Inspection readiness frameworks
- Trial master file quality expectations
- Audit responses
Location
- US
Work Type
- Full-time
- Travel approximately 20%
Experience Level
- Senior Manager
- Minimum of 7 years of progressively responsible US and/or global experience in clinical research
Education Level
- Bachelor’s degree in a scientific discipline
Salary/Compensations
- $136,600 - $171,900
Benefits
- Short- and long-term incentives
- Medical, dental, vision, and retirement savings plans
About the Company
- PTC Therapeutics is a global commercial biopharmaceutical company.
- For over 25 years our team has been deeply committed to a unified purpose: Extending life’s moments for children and adults living with a rare disease.
- At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered.
- We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.
- Visit our website to learn more about our company and culture! Site: www.ptcbio.com
Equal Opportunity
- PTC Therapeutics is an equal opportunity employer.
- We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law.
- We are committed to treating all applicants fairly and avoiding discrimination.