Overview
EMEA Medical Affairs Director, Evidence Strategy. Based in EMEA. The EMEA Medical Affairs Director, Evidence Strategy is responsible for evolving and leading our EMEA strategic evidence generation process across the lifecycle in the Janssen pipeline. The objective is to support rapid, optimal market access and differentiation versus competitor medicines by evidence generation decisions anticipated early in the product lifecycle, extending beyond launch into the mature life cycle.
Key Responsibilities
* Oversee best in class EMEA cross-TA evidence generation strategy:
o Evidence Generation short to long term plans
o EMEA Integrated Evidence Generation and Dissemination Plan
* Lead regional IEGP process for EMEA region:
o train IBVT and CVT teams on their responsibilities and key deliverables
o organize and chair IEGP strategy (Q1) and IEGP tactics (Q2) review
o establish a prioritization for ESO EG investments
o present consolidated plans and seek endorsement from relevant leadership bodies (ESLT, ELT)
* Coordinate EMEA contribution to WW IEGP process:
o align deliverables of EMEA and WW IEGP process
o review and provide recommendation to optimize impact of WW IEGP for EMEA
* Work with VP MAF and VP HEMAR to agree and finalize the above.
* Oversee communication (regionally, locally and globally) and roll out of EMEA plans involving key stakeholders.
* Identify and collate with key stakeholders (ETAHs, TAMALs, GMALs, Opco TA teams) a core set of evidence deliverables and associated timelines that will create value for EMEA
* Incorporate competitive insights cross-TA via new CI tools (Insight Miner) in conjunction with CDS
* Design and track medical and business impact of EMEA IEGP
* Establish collaboration model with EMEA HEMAR team and MAF TA teams and establish a clear set of roles and responsibilities
* Strengthen engagement and processes with key countries to ensure their input
* Identify critical priorities for key countries across EMEA and facilitate early engagement and dialogue between major EMEA markets and global decision-makers
* Identify opportunities to strengthen EMEA input into core company processes, such as early CDP shaping, TPP development, regulatory filing discussions
* Continually assess the need for new organisational capabilities or resources to effectively support cross-TA evidence strategy development
* Input as needed into company processes such as long-range financial planning
1. Essential Knowledge & Skills
* The successful candidate requires extensive Pharmaceutical background and will have demonstrated a Regional mind-set with the ability to assimilate complex science and data quickly. A higher scientific degree is desired e.g. PhD or MD.
* Must exhibit behaviours aligned to the J&J Global Leadership Profile including integrity-credo based actions, collaboration and teamwork, sense of urgency, results driven and people development.
* This position requires up to 10% travel.
* Fluency in English language required
* Fluency in additional EMEA languages an advantage
2. Experience
* A minimum of 8 years of progressive Medical Affairs experience is required with a proven track record of exceptional team & cross-functional leadership.
* Experience with R&D programs and the development of commercial and evidence generation strategy is required.
* More than 5 years being part of teams generating Evidence Generation plans
* More than 5 years being part of teams planning and executing Medical Education plans
3. Other
* The role is EMEA based and is likely to involve extensive travel. The role holder should be based in their current country of residence with access to JJIM offices as needed.
4. Location options
* Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
Seniority level
* Not Applicable
Employment type
* Full-time
Job function
* Health Care Provider
Industries
* Pharmaceutical Manufacturing
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