Description
The Director, Medical Communications and Information is the lead for all scientific communications activities for the global Medical Affairs department (GMA). This individual is a subject matter expert in strategic planning and execution of publication activities, communicating scientific information to a multitude of audiences, and evaluating commercial type material for accuracy and scientific rigor, all while upholding adherence to regulatory and industry standards. This individual will work closely with cross-functional teams, including clinical development, partner companies, medical affairs, regulatory affairs, and external key opinion leaders to ensure that our scientific data is effectively communicated to healthcare professionals, researchers, and the broader medical community.
Role and Responsibilities
- Provide strategic leadership and oversight for all scientific communication and publication activities related to ivonescimab.
- Develop and execute a comprehensive publication strategy that aligns with ivonescimab’s lifecycle in collaboration with Summit’s internal stakeholders and external partner.
- Develop and maintain a robust publication plan, including the identification of key publications, timelines, dissemination opportunities, and target audiences. Ensure compliance with industry standards and ethical guidelines.
- Oversee the creation of high-quality scientific content, including manuscripts, abstracts, posters, slide decks, and presentations. Ensure that all materials are accurate, clear, and adhere to industry regulations, guidelines, and ethical standards.
- Manage the budget for scientific communications and publication activities, optimizing resource allocation for maximum impact.
- As a standing member of the Medical-Legal-Regulatory review committee (MLR), be a subject matter expert for all ivonescimab published data and utilize this expertise while reviewing any external communications material to ensure high scientific and regulatory standards.
- Participation in Cross-Functional teams and manage an end-to-end publications process.
- Oversee and mentor one or more employees and manage their performance in adherence to Summit’s performance evaluation standards and company values.
Experience, Education and Specialized Knowledge and Skills
- Advanced degree (PhD or equivalent) in life sciences or related field highly preferred, candidates with a master’s degree in life sciences and extensive relevant experience will be considered.
- Minimum of 5 years of experience in a relevant role within the pharmaceutical industry required, a strong focus on oncology preferred.
- Strong clinical/scientific acumen required including the ability to interpret, analyze, organize, and communicate scientific data.
- Strong interpersonal and communication skills with the ability to work effectively in a cross-functional, matrixed organization.
- Experience working with KOLs, and academic institutions is a plus.
- Ability to interact with senior management, academic experts, and patient advocates appropriately, with confidence and ease.
- Proficient user of standard MS Office suite (e.g., Word, Excel), experience using electronic document management systems, and document review tools.
- Strong computer and database skills
- Attention to detail, accuracy, and confidentiality.
- Excellent organizational skills
- Critical thinking, problem solving, ability to work independently.
- Must be able to effectively multi-task and manage time-sensitive and highly confidential documents.
- Work in a fast-paced, demanding, and collaborative environment.
