Job Description

A world leader in developing and commercializing innovative biopharmaceuticals for rare diseases driven by genetic causes. Throughout, we’ve worked tirelessly to make a difference by pursuing bold science while respecting, educating, and connecting with patients. Through our expertise in genetics and molecular biology, we have been able to develop targeted therapies that address the root cause of the exact conditions we seek to treat.

We are a dynamic team of research and scientific professionals who are passionate about turning science and innovation into medical solutions. Through our diversity, scientific knowledge, professional rigor and focus on innovation, we are merging our technology with the drug development expertise to unlock cures to many therapies.

Senior Manager, Global Medical Affairs Resource

Job Description:

Major Duties and Responsibilities:

May include but not limited to the following:

The primary responsibility of this role is to develop and maintain a patient-specific clinical trials website. The ideal candidate will have the ability to work independently and possess experience in medical writing for both patient-specific audiences and scientific audiences.

• Write and edit content for both patient-specific audiences and scientific audiences, ensuring accuracy and clarity.
• Develop and maintain a patient-specific clinical trials website. Ensure the website is user-friendly, informative, and accessible to patients seeking clinical trial information.
• Monitor website analytics and user feedback to continuously improve content and user experience.
• Collaborate cross-functionally to develop scientific content and resources, including scientific/clinical slide decks, educational and training materials, field resources for external use and digital omnichannel assets.
• Develop project timelines and ensure on-time delivery of resources; effectively communicate project timelines and project status to stakeholders
• Manage vendors as needed
• Manage all technical aspects of Medical Review Committee (MRC) reviews and approvals, including annotations, referencing, and comment adjudication, in collaboration with clinical subject matter experts and MRC members and administrators
• Adhere to SOPs, work instructions, and quality standards
• Apply legal, regulatory, and compliance requirements to all Medical Affairs activities

Skills

• Experience creating scientific and patient-specific resources in a pharmaceutical, biotech, or agency/vendor setting
• Scientific/clinical background in hematology and/or oncology, preferred
• Digital omnichannel delivery of scientific content experience preferred
• Excellent interpersonal communication, presentation, strong personal integrity, teamwork abilities, and customer focus are necessary with demonstrated superior written and verbal communication skills required.
• Expert working knowledge of Microsoft Office Suite
• Expertise in Adobe Creative Suite including Illustrator preferred
• Experience in Veeva strongly preferred
• Familiarity with SharePoint and project management software preferred
• Knowledge of HTML, CSS, and other web development languages preferred
• Familiarity with SEO best practices and digital marketing strategies preferred

Required

• HEMATOLOGY
• EXCELLENT WRITTEN AND VERBAL COMMUNICATION SKILLS
• PROJECT MANAGEMENT
• MEDICAL WRITING
• MICROSOFT OFFICE

Additional

• HTML
• DIGITAL MARKETING
• SHAREPOINT
• CLINICAL TRIAL
• CSS
• ILLUSTRATION
• USER EXPERIENCE
• SOPS
• ONCOLOGY
• CLINICAL TRIALS
• SEARCH ENGINE OPTIMIZATION
• MEDICAL REVIEW
• ADOBE ILLUSTRATOR
• DIGITAL CAMPAIGN
• MICROSOFT SHAREPOINT
• ILLUSTRATOR

Education

• MS degree or higher (PhD or Pharm.D) with 3-5 years’ experience in pharmaceutical or agency medical affairs experience

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