Senior Manager, Clinical Operations

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

Job Description Summary:

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.
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Job Description:

ESSENTIAL FUNCTIONS

Primary duties/responsibilities:

Clinical Trial Management

• Lead or support the operational execution of Phase I-IV clinical trials, depending on study complexity and program needs.
• 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
  •  Vendor scopes of work and operational budgets
• Oversee study start-up, conduct, and close-out activities.

Clinical CRO and Service Provider Oversight

• 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.

Cross-Functional Collaboration

• Partners 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.

Study Oversight and Compliance

• Ensure clinical trials are conducted in accordance with:
  • ICH-GCP guidelines
  • Applicable global regulatory requirements
  • 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.

Site and Study Support

• 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.

Budget and Timeline Management

• 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.

Team Leadership and People Management

• May 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.

Documentation and Reporting

• Contributes to preparation of study management plans, service provider oversight documentation, and operational reports.
• Provides 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.

Performs other tasks and assignments as needed and specified by management. 

 

KNOWLEDGE/SKILLS/ABILITIES REQUIRED

* Minimum level of education and years of relevant work experience.

 

• 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.

 

* Special knowledge or skills needed and/or licenses or certificates required.

 

• 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.

 

*Special knowledge or skills and/or licenses or certificates preferred.

 

• Experience executing clinical trials in rare disease populations
• Experience working with global centers of excellence and highly specialized investigative sites.
• Experience with strategic CRO partnership models and formal service provider oversight documentation
• Working knowledge of risk-based quality management frameworks
• Familiarity with inspection readiness frameworks, trial master file quality expectations, and audit responses.

 

* Travel requirements

 

• Approximately 20%

Expected Base Salary Range: $136,600 - $171,900. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.

 

In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC’s medical, dental, vision, and retirement savings plans.

 

EEO Statement:

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.

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