Clinical Trial Associate Role at PTC Therapeutics, Inc., USA
PTC Therapeutics Inc is hiring for an exciting clinical trial job opportunity for the position of Clinical Trial Associate I. This hybrid, full-time role is based in New Jersey and supports global clinical operations focused on rare and serious diseases. If you are an experienced clinical trial associate looking to grow your career in a purpose-driven biopharmaceutical company, this role offers strong exposure to end-to-end clinical trial activities.
Job Details:
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Job Title: Clinical Trial Associate I
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Job Requisition ID: R3685
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Job Type: Full Time
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Work Mode: Hybrid
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Location: USA – New Jersey – Warren
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Department: Clinical Operations
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Travel Requirement: 10–15%
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Posted On: Posted Today
About the Company:
PTC Therapeutics Inc is a global commercial biopharmaceutical company with over 25 years of experience advancing innovative therapies for rare diseases. The company is driven by a unified purpose of extending life’s moments for children and adults living with serious conditions. PTC Therapeutics Inc promotes an inclusive, diverse, and empowering workplace culture where employees feel valued and supported. Explore more clinical trial job offers.
Educational Requirements:
- Bachelor’s degree in a life science or healthcare-related discipline
- Minimum 2 years of clinical research support experience in pharmaceutical, biotechnology, or related industries
- Equivalent education and experience may be considered
Key Responsibilities of Clinical Trial Associate Role:
- Support clinical trial start-up, maintenance, and close-out activities
- Assist in collection, review, and tracking of essential clinical and regulatory documents
- Maintain and organize the Trial Master File (TMF) ensuring ICH-GCP compliance
- Coordinate study meetings, prepare agendas, and document meeting minutes
- Interface with CROs, vendors, and investigator sites
- Support CTMS updates and ensure accuracy of trial data
- Participate in monitoring oversight and co-monitoring visits
- Support audit preparation and TMF quality control activities
Skills Required for Clinical Trial Associate Role:
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Familiarity with clinical trial documentation and processes
- Experience working with Trial Master Files (TMF)
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong written and verbal communication skills
- Excellent organizational, planning, and time management abilities
- Ability to work in a fast-paced, cross-functional environment
Benefits of the Clinical Trial Associate:
- Competitive salary range: $81,900 – $103,100
- Short-term and long-term incentive programs
- Medical, dental, and vision insurance plans
- Retirement savings plans
- Career growth in a global biopharmaceutical organization
- Opportunity to work on impactful clinical trial programs for rare diseases
