Nema Medical advisor Hematology at Johnson & Johnson

The Responsibilities & The Impact YOU Will Have

• Develop and maintain detailed knowledge in products, market trends, competitor activities etc.
• To provide expertise to the NEMA Medical Affairs Functional Network
• To provide expertise to NEMA Operating Company functions (BTs, Medical, Commercial, HEMAR Regulatory Affairs etc.)
• To have a pro-active role in the NEMA CVTs and the Medical Affairs functional network to provide input into and support the implementation of the NEMA MAF Strategy and Plan:
• Work with the CVT Team to gather input for the NEMA Medical Affairs Product Plan(s) for designated product(s)
• Work with Medical Affairs functional network to drive the implementation of the Strategy and Plan
• Support effective and regular communications between CVT and local MAF teams, including regular communications to help minimise duplication of advocacy and access programmes across countries, and facilitate co-ordination between Medical Affairs, Marketing, HEMAR, and individual countries
• Provide input into local publications plan
• Provide input into Medical Education plans/activities in NEMA countries
• Support operating companies in developing, aligning, and implementing th eirImmunology product strategies and tactical plans.
• Support and liaise with the EMAD in communication and feed-back to Global MAF.

External Relationships

• To build up or enhance a trusted collaboration with the external scientific community in order to facilitate a continuous communication and transfer of knowledge between the company, thought leaders and a wider group of physicians and customers.
• To leverage relationships with investigators, NEMA thought leaders and patient groups to gain input into the development of the product strategy and to specific protocols.

Study Planning and Execution

• Support Medical Affairs of NEMA countries to evaluate Investigator Initiated Study (IIS) proposals for scientific soundness and whether those are in alignment with the medical strategy.
• Support all Early Access Programs (EAPs) related activities. Give input and actively support the Program Leader.
• Support Investigator Initiated Studies (IIS), by interactions with Investigators, respecting the internal procedures, and monitoring of the milestones planed in the agreement.
• Work with and support the EMPL and GCO-MAO in the oversight of IIS according to internal procedures including.
• Janssen Standard Operating Procedures (SOP) and Health Care Business Integrity (HCBI), and legal regulations.
• To act as Study Responsible Physician (when the Medical Advisor is a qualified medical doctor) or Study Responsible Scientist.

Publications

• Support the development and implementation of the NEMA MAF publication plan at local level.
• Support efforts that ensure that J&J guidelines for publication of studies are followed, and that all MAF studies (local and EMEA) are published in accordance with J&J policy. Ensure NEMA messages relating to allocated product(s) (including core medical education materials, abstracts, medical information materials, marketing materials etc.) accurately reflect scientific data and are fully compliant with applicable regulations.

Medical Education

• For pan-NEMA Medical Education activities, support the NEMA Medical Education Coordinator on Medical Education programs concept, review the program proposals and final program outline and support the review of scientific Medical Education materials in collaboration with Medical Information.

Materials

• Support review of Medical Affairs Materials (slide decks, Q&A...)
• Support local NEMA countries training needs in drug/disease area.

Other Activities As Required

• Provide input to NEMA business development initiatives for allocated product(s). When requested Partner with the late lifecycle management group to provide proactive medical input for lifecycle extension opportunities as appropriate.

Accountabilities

• Support implementation of the NEMA Medical Affairs Strategy and Plan at local level.
• Enhance collaboration with external scientific community (incl. IIS).
• Support NEMA countries as expert with the implementation of tactical plans.
• Support review of product NEMA Medical Education Programs and scientific materials.
• Support medical review and approval of market research and promotional materials in accordance with internal procedures and applicable external regulations.
• Manage CVT allocated medical budget.

Compliance Responsibilities

• Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOPs (Standard Operating Procedures) are met and, where applicable, appropriately managed when planning projects, developing materials, executing projects and contracting vendors.
• Ensure HCC and legal requirements (Fair Market Value, Transfer of Value rules, Promotional Materials rules) are fully understood, appropriately managed and, where applicable, complied when planning projects, developing materials, executing projects and contracting vendors.
• Ensure inspection readiness with respect to personal training compliance, and availability of recent CV and individualized Job Description.

Qualifications
We’d love to hear from YOU, if you have:

Required

• Scientific degree: Medical Doctor, Pharmaceutical or Science, PhD university degree.
• Minimum of 4-5 years of pharmaceutical or medical affairs experience.
• Experience in the Hematology TA required.
• Experience working cross functionally in a matrix environment (a plus).
• Experience leading with no direct authority (a plus).