[Hiring] Contractor, Global Scientific Communications @PTC Therapeutics, Inc.

Role Description

The Contractor of Scientific Communications will be responsible for the development and execution of the scientific communications strategy across the portfolio, leading day-to-day publication planning, congress activities, and scientific content development. This individual partners closely with the Senior Director, Global Scientific Communications and cross-functional stakeholders in Clinical Development, Regulatory, Medical Affairs, and Commercial to translate scientific data into clear, compliant, and scientifically rigorous materials for internal and external audiences. The role requires strong strategic thinking, scientific writing ability, project management skills, and comfort operating in a fast-paced environment.

Qualifications

• An advanced medical or scientific degree (MD, PharmD, PhD, MS, MPH) is required.
• 5+ years of experience in Biopharmaceutical/Healthcare industry, preferably within a matrix structure and within Scientific Communications roles.
• Relevant experience in other Medical Affairs roles (e.g. Medical Science Liaison, Medical Information) will be considered.
• Expertise in Scientific Publications, including planning and execution across phases of drug development and commercialization.
• Deep knowledge of scientific publication standards, data disclosure requirements, and medical compliance, including GPP4 and ICMJE guidelines is required.
• Expertise in Medical Education approaches and best practices is required.

Requirements

• Effectively communicates complex scientific and clinical data to internal and external stakeholders.
• Ability to collaborate and build solid working relationships cross-functionally.
• Ability to manage multiple projects simultaneously, think critically, and adhere to deadlines.
• Attention to detail.
• Experience in orphan/rare diseases, molecular biology, metabolic disorders, neurology and/or genetic disorders.
• In-depth knowledge of Good Publication Practices (GPP4) and other relevant industry standards (ICMJE, CONSORT, etc.), Sunshine Act, relevant Codes of Conduct (e.g. PhRMA, EFPIA), and other guidance related to post-marketing practices and scientific data communication.
• Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
• Demonstrated expertise in Publications planning and the development and implementation of Scientific Publications.
• Building credibility with cross-functional partners across Clinical Development, Regulatory, Commercial, and Medical Affairs.
• Exercising sound judgment and independent problem-solving in a fast-paced environment.
• Translating complex clinical and scientific data into clear, audience-appropriate narratives for diverse stakeholders.
• Excellent project management and organizational skills, with ability to manage multiple concurrent projects and timelines.
• Excellent verbal and written communication skills; ability to influence without authority.
• Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
• Demonstrated experience and ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external stakeholders.
• Proficiency with Microsoft Office Suite, Publications and Medical materials management platforms (e.g. Pubstrat, Veeva MedComms) and video conferencing platforms.
• People and project management experience.
• Fluent in English (verbal and written).
• 5-15% travel required.

Benefits

• Expected Hourly Range: $80 - $130/hour.
• The hourly 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.

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.