National Medical Manager

Celltrion Healthcare Ireland-Dublin, Ireland

Company: Celltrion Healthcare Ireland Ltd.

Job location: Dublin office (Ireland), or Waterford office (Ireland)

Workplace type: Office based (but partial field work required)

Job Summary:

  • The National Medical Manager is responsible for providing balanced, non-promotional high-level scientific and technical partnership to internal and external stakeholders for the benefit of patient care.

Accountability:

  • Develops and executes Irish medical strategies and medical plans that are conducive to the strategic advantage of the company.
  • Understands the commercial strategy and provides scientific support to enable compliant delivery aligned with the medical plan.
  • Collaborates with management and appropriate personnel to execute the medical plans in the field (ABMs, RTMs, consultancies, speakerships, research, authorships etc.)
  • Identifies, collects, and internally provides insights into medical and scientific field intelligence (e.g. competitor research and medical strategies, educational activities)
  • Creates professional and credible relationships with Key Opinion Leaders and experts.
  • Identify the gaps in clinical data and when requested, facilitate further clinical studies/IITs and advisory boards
  • Ensure that any unsolicited request for information from healthcare professionals (HCPs) is provided in an unbiased and accurate manner.
  • Supports internal training to ensure Celltrion teams receive up to date scientific, clinical, and therapeutic updates in accordance with company approved materials.
  • Act as "Scientific Service" (Compliance lead) according to the IPHA code: review SMPC, artwork, and approve marketing materials for IPHA compliance
  • Be main agency coordinator for PV (MI, AE reporting, aRMMs version control etc.) and Quality Assurance.
  • Communicate with regulatory bodies when necessary (HPRA in case of inspections).

Key Responsibilities:

  • Provide information and technical support to HCPs including significant changes in marketing authorisation (particularly in relation to safety), scientific publication relating to the therapy area or a product and potential clinical trial enquiries and Clinical Trial site visits to provide Celltrion medical support.
  • Attends appropriate scientific congresses, regional/local field meetings to develop knowledge regarding current developments and clinical advances in the relevant therapy areas; shares learnings and insights with wider cross functional teams.
  • Take personal responsibility for updating knowledge on an ongoing basis
  • Provide scientific support and input to training and the wider teams
  • Work in collaboration with the commercial lead and product manager for the development of training/promotional materials
  • Provide Medical partnership to HCPs
  • Support speakers speaking at Celltrion initiated scientific meetings
  • Maintain compliance and diligence in archiving activities
  • Escalates any decisions, or seek the support of colleagues or management if personal knowledge and understanding is not at the level required to carry out any part of the role.
  • Ethical Leadership; Inclusive Leadership; Environmental and Safety Leadership
  • Care for his/her own/others' safety, and to cooperate with the company to ensure a safe place of work.
  • conform to Company safety rules and procedures / Report any accidents of personal injury or property damage / Assist in the investigations with the objective of introducing measures to prevent recurrence / Escalate any doubts or uncertainties to their supervisor and/or manager.

Basic Qualifications:

  • Minimum 8 years of work experience (preferably 4+ years of work experience in pharma industry)
  • Previous experience as a Medical Science Liaison and Medical Advisor
  • Eligible for compliance review

Core Competencies:

  • Excellent communication and presentation skills, experienced in the delivery of scientific presentations
  • Final Medical Signatory
  • Adaptable, independent, and proactive working style
  • Knowledge of the pharmaceutical industry, local regulatory processes/healthcare system, including the ability to understand clinical priorities and how processes work within this system
  • Thorough knowledge of all products and disease areas
  • Competent to critically appraise studies and clinical evidence so as to allow engagement on higher scientific level with customers
  • Professional and timely response to both internal and external requests.

Education:

  • Pharmacist or Doctor certified (eligible for final signatory)

Application question(s):

  • Do you have minimum 8 years of work experience?
  • Are you a certified pharmacist or doctor?

Work Location: In person