
Senior Director, Medical and Scientific Communications
Posted Oct 15

Posted Oct 15
This is a fully remote position, open to applicants in California.
• Oversee the formulation and implementation of Vera’s publication and scientific congress strategy.
• Create and sustain a comprehensive publication roadmap that includes manuscripts, abstracts, posters, oral presentations, encore presentations, and various scientific communications.
• Transform clinical development plans, data readouts, and milestones into effective publication and congress strategies.
• Generate scientific content and evidence-based messaging that aligns with the medical and scientific communication platform.
• Direct the planning and execution of scientific congresses, covering abstracts, posters, and oral presentations.
• Compose, revise, and critically assess manuscripts, abstracts, posters, oral presentations, and scientific slide decks.
• Manage the complete publication development process from conception and data availability to submission, presentation, publication, and post-publication activities.
• Facilitate internal and external author reviews while fostering relationships with investigators and external authors.
• Ensure that publications adhere to GPP, ICMJE, company policies, and the requirements of journals and congresses.
• Collaborate with Clinical Development and Biostatistics to analyze clinical datasets and convert them into scientific communications.
• Act as a scientific communications partner for Clinical Development, Biostatistics, Medical Affairs, Clinical Operations, Regulatory, and Commercial teams.
• Evaluate cross-functional materials for coherence with the approved scientific narrative and evidence.
• Identify risks, gaps, or inconsistencies in scientific communication and propose solutions.
• Enhance publication planning and development processes, workflows, governance, templates, tools, and review procedures.
• Monitor publication status, deadlines, dependencies, author reviews, and key decisions; provide progress metrics and reports.
• Coordinate the cross-functional publication planning committee.
• Supervise external medical communications agencies, publication vendors, and freelance medical writers.
• Develop publication and congress forecasts while managing delivery within the Medical and Scientific Communications budget.
• Travel up to 30% for congresses, advisory meetings, and other business engagements.
• Advanced scientific or clinical degree (PhD, PharmD, MD, or equivalent) in a relevant field.
• At least 10 years of experience in scientific communications, medical writing, or publications within the biotechnology, pharmaceutical, or medical communications sectors.
• Minimum of 8 years of direct experience in medical writing and scientific publications, including the development of peer-reviewed manuscripts and scientific congress presentations.
• Proven experience in developing and executing strategic publication plans for clinical-stage programs.
• Strong comprehension of clinical development and the ability to interpret clinical trial data, statistical analyses, tables, figures, and other data outputs.
• Experience collaborating directly with Clinical Development and Biostatistics to translate intricate clinical data into scientific publications and communications.
• Exceptional skills in scientific writing, editing, and critical review.
• Demonstrated experience managing publication development and external author reviews.
• Familiarity with Good Publication Practice (GPP), ICMJE authorship guidelines, and relevant publication standards and ethical requirements.
• Working knowledge of healthcare compliance requirements governing medical communications, including pertinent OIG, PhRMA, and EFPIA guidelines.
• Proven ability to manage external medical communications agencies and vendors.
• Capability to juggle multiple complex projects, priorities, and deadlines in a dynamic biotechnology environment.
• Strong interpersonal and influencing skills with an established ability to foster alignment across cross-functional teams.
• Scientific training or research experience in nephrology, immunology, or a closely related field (preferred).
• In-depth scientific understanding of nephrology, immunology, autoimmune diseases, or related therapeutic areas; experience with IgA nephropathy or related glomerular diseases is a plus (preferred).
• Experience in formulating long-range publication strategies that integrate clinical development milestones, statistical analyses, congress opportunities, and manuscript planning (preferred).
• Experience in supporting scientific communication platforms and core scientific narratives (preferred).
• Prior leadership experience in a publications or medical communications role (preferred).
• Certified Medical Publication Professional (CMPP) credential (preferred).
• Annual performance incentive bonus.
• New hire equity.
• Ongoing performance-based equity.
• Medical insurance.
• Dental insurance.
• Vision insurance.
• 401k match.
• Flexible time off.
• Paid holidays.
AbbVie
AbbVie
Pfizer
Pfizer
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