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UCB Pharma

Biopharmaceuticals for neurology and immunology therapies

Medical Communications Specialist

Regulatory & Quality (Life Sciences)Posted on Nov 9
Full-timeAtlanta, GA, USA$108k - $142k /yr

About the Job

Requirements

  • A doctorate (M.D., PharmD., or Ph.D. in a scientifically relevant field) is required.
  • At least 1 year of Medical Affairs experience, including medical writing and MLR medical review experience in the pharmaceutical industry, is required.
  • Strong medical writing skills and the ability to analyze, interpret, understand, and summarize highly complex scientific data are required.
  • Attention to detail is required.
  • Strong interpersonal skills and excellent written and verbal communication skills, including proficient use of English grammar, punctuation, and spelling, are required.
  • Proficient literature-searching skills are required.
  • Strong business acumen and a solid understanding of the pharmaceutical industry are required.
  • The ability to lead projects with a proactive and collaborative approach to problem solving is required.
  • The ability to clearly articulate complex scientific concepts in one-to-one and group settings is required.
  • A high level of accountability to deliver superior content in a fast-paced, dynamic environment is required.
  • Strong time-management and organizational skills, with proficiency in Microsoft Office applications and reference-management software, are required.
  • Successful completion of initial training and all assessments is required.

Responsibilities

  • Develop and maintain deep therapeutic-area and product knowledge.
  • Serve as a scientific resource for internal stakeholders.
  • Apply scientific and product knowledge, synthesize complex data, and communicate it in understandable and useful written and verbal formats to individuals and groups.
  • Respond to unsolicited medical-information requests from healthcare professionals and other external stakeholders.
  • Conduct comprehensive searches and critically evaluate medical and scientific literature.
  • Develop timely written medical-information response documents, including standard response letters, Medicaid Summaries, and AMCP Formulary Dossiers, that are comprehensive, cohesive, focused on key information relevant to the request, and consistent with the department style guide.
  • Lead database planning and launch activities to maintain an accurate and up-to-date Enclosure and standard-response-letter repository.
  • Manage the Medical Information mailbox daily to ensure escalated spontaneous medical-information requests are addressed appropriately.
  • Establish relationships and build credibility with internal and external customers through appropriate scientific, medical, and product-specific information exchange.
  • Support scientific publications as appropriate.
  • Support and review scientific and promotional materials with medical sign-off, collaborating with Legal, Compliance, and Regulatory colleagues for cross-core teams as needed.
  • Engage in planning and executing congress activities, including medical-booth support, Congress Lead, and Topic Team Lead activities.
  • Support scientific training and collaborate to deliver new-hire and advanced presentations on disease state and product clinical data.
  • Lead the planning and execution of Medical Communications Initiatives.
  • Apply sensitivity to legal and regulatory issues affecting industry-based medical-affairs practice.
  • Manage vendor relationships as appropriate.
  • Follow UCB compliance and professional standards and apply ethical decision-making practices and guidelines in all aspects of the organization.
  • Participate in other projects and duties as assigned.
  • Travel overnight occasionally, up to 20%.

Desired Qualifications

  • Three or more years of Medical Affairs experience in the pharmaceutical industry is preferred.
  • Experience in rheumatology, gastroenterology, dermatology, or general immunology is strongly preferred.
  • Product launch experience is preferred.

About the Company

UCB Pharma

Biopharmaceuticals for neurology and immunology therapies

UCB Pharma focuses on developing treatments for severe diseases in neurology and immunology. It discovers, develops, and commercializes novel molecules and generates products aimed at improving patient lives. The company works by researching and developing therapies, integrating patient insights to guide innovation, and investing over a quarter of revenue into scientific research. Its global presence (about 9,000 employees across 40 countries) and €5.3 billion 2023 revenue reflect its scale and commitment to bringing therapies to patients worldwide. UCB differentiates itself by combining direct patient engagement with substantial R&D investment to address unmet needs in neurology and immunology, aiming to transform lives through science and patient care.

Company size
10,001+
Company stage
IPO
Headquarters
City of Brussels, Belgium
Founded
1928

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