(Senior) Medical Scientific Liaison (m/f/d) Oncology

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

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(Senior) Medical Scientific Liaison (m/f/d) Oncology

This position can be filled as MSL or Senior MSL, depending on experience and qualifications

The role of a Medical Scientific Liaison (MSL) is to be a therapeutic area scientific expert, responsible for proactively or reactively discussing our products, treatment trends incl. unmet medical needs, scientific insights, studies and projects with Leading Specialists (LS). The MSL provides fair, balanced, objective, scientific information and education to health care professionals on a peer-to-peer basis and to internal partners, as required by scientific and business needs. The MSL executes activities described in the country specific MAF plan. Through strategic and key stakeholder engagement, the MSL builds and maintains external relationships with leading specialists and represents the primary MAF contact. In addition, MSLs captures and logs external medical insights and use these insights to inform the medical affairs - and CVT strategy. The MSL role has a predominantly external/field focus.

A job holder of the role of a MSL / Senior MSL will

• have demonstrated a long-term commitment for medical affairs and the role of MSL based on track record of success with consistent satisfactory performance on both the achievement of objectives as well as the attitude and behaviours demonstrated
• have established and effectively cultivates a solid long term network of LS within the therapeutic area and is genuinely recognized by these leading specialists as a trusted counterpart and a collaborative partner
• be able to quickly obtain insights and identify emerging scientific concepts and its potential future clinical implications
• have an extensive medical and scientific product and disease knowledge within the therapeutic area
• have demonstrated strategic capabilities to translate the medical affairs strategy into and impactful region/country specific tactical
• have the ability to identify and act upon new strategic opportunities in the healthcare landscape, lead multiple projects independently and pro-actively create, lead and execute stakeholder plans in collaboration with internal partners
• coach other MSL’s within the therapeutic area

Job Responsibilities
Scientific knowledge

• Serve as resource for scientific information, clinical research activity, healthcare landscape and emerging scientific trends within therapeutic area, with demonstration of continuously updated knowledge in these key areas
• Represent the primary MAF contact for the leading specialists and is considered and recognized as trusted scientific partner while building positive reputation of company and MSL team
• Ensure understanding of current scientific landscape through self-driven learnings, internal/external trainings and the collection and logging of medical insights
• Support the Medical Advisor in the organization of advisory boards and participate/contribute as appropriate

External stakeholder management

• Accountable for strategically map, identify, profile and prioritize thought LS in line with the medical plan goals
• Develop and maintain credible peer-to-peer collaborations and relationships with key LS in the assigned therapeutic area
• Accountable for defining, planning and integrating MSL activities into x-functional account plan tailored to the LS’ and product-strategic needs x-functional account planning
• Responsible for executing the MSL activity plan in alignment with medical advisor and cross-functionally
• Identify needs and gaps for medical education contents/formats (e.g. through MESC process) or for related medical projects and ensures their implementation
• Communicate reactively ongoing research including our pipeline, research and development programs and other relevant information
• Serve as Patient Advocacy Group (PAG) - champion per indication in collaboration with PAG lead

Internal stakeholder management

• Lead medical representative in the cross-functional account-planning activities by sharing gained insights and updating Sales colleagues on MSL activities for LS
• Feed key insights back to CVT and x-functional teams to inform their strategies
• Act in close strategic collaboration with the medical advisor
• Receive investigator proposals for IISs and contribute to Medical Affairs department internal decision-process - if appropriate and in collaboration with medical advisor

Data/information generation activities

• Collaborate with GCO and clinical research organizations (CROs) in feasibility, PI/ site selection, management, and issue resolution for R&D clinical trials and MAF studies - if appropriate and in collaboration with medical advisor
• Support the execution of HEMAR projects and/or Real World Data studies/projects
• Lead the customer interaction communication for customer support requests (e.g. educational grants, quality improvement grants, investigator-initiated studies) and ensure appropriate and timely internal discussions for proper follow-up
• Perform field/customer implementation of expanded access programs and risk management programs

Data/information dissemination activities

• Proactively communicate relevant scientific information in accordance with health care compliance guidelines
• Respond to unsolicited scientific queries from customers for approved products and products/indications in development, based on Medical Affairs and Medical Information documents
• Use digital technologies and new media to support compliant proactive and reactive communication
• Provide impactful external presentations in line with the medical affairs tactical plan

Act in full compliance with J&J Credo and HCBI principles to preserve trust and reputation towards HCP and patients using Janssen products. Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOP’s (Standard Operating Procedures) are met. Complete all trainings, documentation and administrative requirements in a timely, accurate and compliant manner

Qualifications
Personal

• Customer centricity and strong external focus
• Strong business acumen with sense of urgency
• Effective collaboration and strong networking skills, ability to build professional relationships with internal and external stakeholders
• Positive dissatisfaction and aspiration to beat the odds
• Effective communicator with strong influencing skills and ability to discuss data (e.g. study results) with HCPs on a peer-to-peer level
• Strategic thinking and analytical skills
• Accountability and excellence in execution
• High learning agility and open mindset for change
• Winning mindset and motivated to work in a high performing team
• Integrity Mindset

Professional

• Scientific degree: Medical Doctor, Pharmaceutical or Natural Science university degree (with MD/PhD being an additional asset)
• Good knowledge of the therapeutic area, strong understanding of scientific research, clinical trial design/conduct and interpretation of medical/scientific data (scientific acumen)
• Ability to work with clinical & scientific data in order to translate these into relevant information for the clinical practice of the HCP and patients (clinical acumen)
• Strong knowledge of Pharma industry and Health Care Environment
• Fluency in English and German or French required, fluency in a 2nd national Swiss language considered an advantage
• 3-5 years related work experience