Senior Clinical Operations Leader for Trials & Strategy

PTC Therapeutics, Inc; New York (NY); On-site; USD 170,000 - 214,000; Full time

Benefits offered by this job

Short- and long-term incentives

Medical, dental, vision coverage

Retirement savings plans

Job summary

PTC Therapeutics, Inc in the United States seeks an Associate Director, Clinical Operations to lead full lifecycle clinical trials across indications. You will work within the clinical team to design, execute, and close studies, while ensuring regulatory compliance and SOP adherence.

The role requires strategic planning, strong communication, and mentoring of team members, with up to 20% travel. Base salary and incentives are provided as part of a comprehensive compensation package.

Qualifications

• Bachelor's degree in a scientific discipline.
• Minimum 7 years of progressively responsible clinical research experience.
• Experience in US/global clinical trials and collaboration with cross-functional teams.

Responsibilities

• Lead planning, execution, and reporting of clinical trials, including timelines, CRF design, site management, and data review.
• Collaborate with internal/external teams to shape clinical strategy and study plans.
• Prepare and edit study documents, informed consent forms, and regulatory submissions.
• Coordinate site lists, negotiate contracts and budgets, and organize investigator meetings.
• Manage study budgets and timelines, and report progress to stakeholders.
• Contribute to regulatory submissions and communications with agencies and IRBs.
• Mentor and supervise direct reports as applicable.

Skills

Clinical trial management

Project management

GMP/GCP/ICH knowledge

Analytical thinking

Communication skills

Education

Bachelor's degree in a scientific discipline

7+ years of clinical research experience

Tools

Microsoft Word

Microsoft Excel

MS Project

Job description

PTC Therapeutics, Inc in the United States seeks an Associate Director, Clinical Operations to lead full lifecycle clinical trials across indications. You will work within the clinical team to design, execute, and close studies, while ensuring regulatory compliance and SOP adherence.

The role requires strategic planning, strong communication, and mentoring of team members, with up to 20% travel. Base salary and incentives are provided as part of a comprehensive compensation package.