About the role
Job Description Summary
Creation of high-quality complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery.
Job Description
Key Responsibilities:
- Research and write original content for publications activities (primary and review manuscripts, abstracts, posters), slide presentations and other materials. Demonstrate a command of assigned therapeutic areas and expertise with assigned products.
- Prepare meeting materials for satellite symposia (agenda, slide content, speaker briefings etc.), and reports from advisory boards and other internal or external meetings. Develop content that is scientifically accurate, evidence-based, grammatically accurate, referenced using appropriate sources, and consistent with quality standards for author review, customer review as appropriate, and scientific peer review.
- Perform internal scientific reviews to ensure quality in line with the scope and scientific messages. Mentor internal team members and help onboard new joiners.
- As needed, perform quality control (QC) checking / proof reading of the above-mentioned documents to meet stakeholder expectations. Clearly communicate medical scientific concepts in a condensed, audience-appropriate way.
- Follow all internal processes and procedures regarding workflow, development of deliverables, and adherence to industry best practices, including GPP. Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed and to work on projects across multiple brands at any given time.
- Provide input and aid in troubleshooting/problem-solving. Participate in strategic and tactical publications planning and related research.
- Maintains records for all assigned projects including archiving in line with global SOPs. Performs additional tasks as assigned.
Essential Requirement:
- Minimum Science degree or equivalent or MSc, PhD, PharmD, or MD.
- Minimum of 5 years’ experience in medical communications and medical writing.
- Good understanding of industry work processes for publications.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
- Excellent written and oral English
Skills Desired
Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)Aplyr's read
Novartis is a Swiss-based global healthcare leader, known for its focus on innovative medicines and commitment to addressing patient needs through diverse roles.
What's promising
- •Novartis invests heavily in research and development, driving innovation in pharmaceuticals.
- •The company offers a wide range of global career opportunities across various fields.
- •Strong focus on cutting-edge therapies, including gene therapy and AI-driven solutions.
What to watch
- •Regulatory challenges can impact the speed of drug approval and market entry.
- •High competition in the pharmaceutical industry requires constant innovation to maintain market position.
- •Complex organizational structure may slow decision-making processes.
Why Novartis
- •Novartis has a robust pipeline of innovative medicines, setting it apart in the healthcare sector.
- •The company emphasizes a diverse and inclusive workplace culture across its global operations.
- •Novartis is a leader in digital transformation within pharmaceuticals, integrating AI and data science.
Aplyr’s read is generated by AI from public sources. Was it useful?
About Novartis
Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. It focuses on innovative medicines, generics, and eye care.
