Contractor, Global Scientific Communications

Job not on LinkedIn

🔥 3 hours ago

🇺🇸 United States – Remote

💵 $80 - $130 / hour

⏰ Full Time

🟡 Mid-level

🟠 Senior

🗣️ Communications

👻 Ghost score 0%

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PTC Therapeutics, Inc.

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1998

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

PTC Therapeutics, Inc. is a patient-centered biopharmaceutical company focused on discovering, developing, and commercializing medicine for children and adults living with rare and serious diseases. They are committed to extending life's moments for patients with rare diseases and their loved ones, specializing in orphan and ultra-orphan disorders, oncology, and anti-infectives.

📋 Description

• Support development and lead tactical execution of Publication and Medical Education plans aligned with asset strategy and medical affairs objectives • Execute publication planning and publication development • Manage global publication activities, including author engagement, abstracts, manuscripts, posters, and oral presentations, in compliance with GPP and company SOPs • Serve as scientific lead and reviewer for publication deliverables, identifying data gaps, inconsistencies, and interpretation risks and driving resolution with cross-functional SMEs • Oversee plans and activities for major international and regional medical meetings, including content development and internal alignment • Own scientific content, including slide decks, scientific exchange materials, and FAQs for Field Medical teams • Partner with cross-functional teams to ensure accurate interpretation and timely dissemination of data • Maintain publication trackers, timelines, and vendor/agency relationships for on-time, on-budget delivery • Support advisory boards, investigator meetings, and external scientific forums • Assist in establishing processes and standards for consistency and compliance across scientific materials • Keep internal colleagues informed of Publications and Medical Education activities • Manage agency partner performance • Provide scientific review of Scientific Communications materials • Cooperate with Global Medical functions and Regional Medical teams • Contribute to Medical Education and Publications best practices, standards, and systems • Collect and provide metrics measuring medical education programs and scientific publications • Support planning and management of the Scientific Communications budget • Maintain and expand therapeutic-area, disease, and product knowledge

🎯 Requirements

• 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 • Experience in orphan/rare diseases, molecular biology, metabolic disorders, neurology and/or genetic disorders • In-depth knowledge of Good Publication Practices (GPP4), ICMJE, CONSORT, Sunshine Act, relevant Codes of Conduct (e.g. PhRMA, EFPIA), and 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 development and implementation of Scientific Publications • 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 • Demonstrated experience working independently and collaboratively in a fast-paced, matrixed, team environment • 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

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