Global Senior Director, Clinical Development Strategy

PTC Therapeutics, Inc.

New York (NY)

On-site

USD 289,000 - 364,000

Full time

5 days ago
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Job summary

PTC Therapeutics, Inc. is a global biopharmaceutical company focused on extending life for those with rare diseases. The Senior Director, Clinical Development provides strategic input across all phases of drug development and oversees CDPs, trials, and external collaborations.

The role requires MD with 5+ years in clinical drug development, leadership of multi-country programs, and strong regulatory submission experience, with travel up to 30%. Base salary ranges stated below.

Qualifications

  • MD degree and at least 5 years of clinical drug development experience.
  • Proven ability to lead large, multi-country clinical development programs.
  • Experience in regulatory submissions and interactions with authorities.
  • Strong verbal and written communication skills.

Responsibilities

  • Leads, contributes to and directs PTC’s global clinical development strategy for his/her assigned indication and/or therapeutic area.
  • Manages relationships with external partners (CROs, vendors, consultants) and monitors budgets to enable CDP delivery.
  • Medically responsible for clinical studies.
  • Facilitates communication with internal and external stakeholders to support CDPs and regulatory submissions.
  • Ensures adherence to GCP regulations and company SOPs.
  • Represents the Clinical Development team in meetings with external collaborators and reviewers.

Skills

Clinical development leadership
Regulatory submissions
Cross-functional collaboration
Budget/contract management
People management

Education

MD degree
Board certification or equivalent

Tools

Microsoft Office

Job description

PTC Therapeutics, Inc. is a global biopharmaceutical company focused on extending life for those with rare diseases. The Senior Director, Clinical Development provides strategic input across all phases of drug development and oversees CDPs, trials, and external collaborations.

The role requires MD with 5+ years in clinical drug development, leadership of multi-country programs, and strong regulatory submission experience, with travel up to 30%. Base salary ranges stated below.

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