Contractor, Clinical Operations: Trial Leadership

PTC Therapeutics, Inc; Warren Township (NJ); On-site; USD 83,000 - 110,000; Full time

Job summary

PTC Therapeutics, Inc is seeking a Contractor, Clinical Operations to lead end-to-end management of clinical trials across indications. You will work within a cross-functional team to plan, execute, and report trials, ensuring regulatory compliance and quality.

The role emphasizes collaboration with investigators, sites, and vendors, with responsibilities for timelines, budgets, and submission activities in a fast-paced environment.

Qualifications

• Bachelor's degree in a scientific discipline with 7+ years of clinical research experience in pharma, biotech, CRO, or related settings.
• Strong working knowledge of the drug development process and GMP/GCP/ICH guidelines.
• Experience with study design, data acquisition, analysis, and reporting.
• Proven ability to influence without direct authority and to work in cross-functional teams.

Responsibilities

• Lead planning, execution, and reporting of clinical trials and timelines.
• Manage sites, CROs, budgets, and investigator meetings.
• Support regulatory submissions and EC/IRB interactions.
• Prepare and review study documents and reports for regulatory agencies and journals.

Skills

Clinical operations

Project management

Regulatory submissions

Communication

Education

Bachelor's degree in a scientific discipline

Tools

Microsoft Word

Microsoft Excel

Job description

PTC Therapeutics, Inc is seeking a Contractor, Clinical Operations to lead end-to-end management of clinical trials across indications. You will work within a cross-functional team to plan, execute, and report trials, ensuring regulatory compliance and quality.

The role emphasizes collaboration with investigators, sites, and vendors, with responsibilities for timelines, budgets, and submission activities in a fast-paced environment.