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International Pharmaceutical Company

Descripción

Establish and foster professional collaborations with the Healthcare community:

• Map the scientific expertise: Identify, complete and update Thought Leaders (TL) database in the disease area in accordance with the Medical Operations and Medical Affairs Therapeutic Areas directives
• Conduct fair and balanced scientific exchanges with TL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings (congresses, symposia, etc.), potential research collaborations
• Identify opportunities for collaboration with TL when aligned with strategy
• Develop and enhance scientific and educational collaborations with HealthCare Professionals (HCPs) within the Healthcare community and act as a medical contact for TL and external medical experts
• Reactively interact to unsolicited and documented queries/requests for information from HCPs

• Reactively on products (on‐label & off‐label indications), or on compounds in development
• Proactively on products (on‐label single‐product presentation) but mainly on disease area management
• Organize or support legitimate scientific exchange meetings
• Contribute to/implement medical education programs in the field
• Contribute to the scientific publication program, if required
• Organize satellite symposia in regional (in‐country) congresses

• Collect, analyse, and report actionable scientific insight from HCP related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment
• If appropriate, organise or support Advisory Boards at Regional level (in‐country)
• Attend and report insights from major National and Regional medical congresses
• Engage and collaborate on specific initiatives with patient organisations in accordance with external/internal global and local guidance's on Interactions with Patient Organisations and individual patients
• Contribute to the dissemination of the information within the Company where appropriate
• Report spontaneous adverse events and product‐related quality complaints in accordance to global and local Accord Healthcare SOP and the local law

• Coordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs' objectives
• Support ICTAS Sponsored Studies (Phase I to IV) operations (see attached Annex), when appropriate
• Identify and drive opportunities to generate real‐world‐evidence data

• Develop Local Medical Plans
• Develop publication and scientific project plan
• Set-up and schedule medical ad board
• Develop local standard responses, if required (in coordination with Medical Information Department)
• Collaborate with commercial staff (Marketing, Sales or NPL team)
• Provide scientific expertise and training to commercial staff as requiredReview and approve promotional materials in accordance with the local SOP and local law
• Contribute to the review and approval of non‐promotional materials in accordance with the local SOP
• Attend the local brand teams to bring additional scientific perspective
• Attend and contribute to regional account planning/training sessions
• Ensure speakers briefing for promotional meetings
• Support Market Access, Regulatory and Healthcare Compliance
• Responding to requests to support hospital formulary submissions and upon request to present the scientific data on Accord Healthcare products
• Responding to scientific inquiries to deliver scientific presentations on the disease area and on the product Responding to request to support dossier or material preparation
• Ensuring all local activities and materials are in line with all local codes

Perfil Buscado (H/M/D)

• Biomedical, Scientific University education ideally to post-graduate degree level e.g. MSc, PhD, MD, PharmD
• Must have at least 5 years of experience as MSL / Medical Advisor in pharmaceutical industry within ONCOLOGY
• Expert/fluent communicator in their local language and excellent knowledge of written and spoken scientific English
• Experience in delivery of scientific presentations and development of relationships with Thought Leaders is strongly preferrence
• Ideally, knowledge in data analysis and statistics for purpose of understanding clinical study result
• Ideally, current working knowledge of legal, regulatory, and compliance regulations and guidelines relevant to industry interactions with health-care professionals
• Convey scientific information briefly, clearly, and precisely
• Possesses a scientific qualification with significant scientific and/ or medical/clinical experience
• The ability to understand, process, communicate and present scientific information to a high standard
• Possess excellent presentation skills
• External customer focus with strong networking capabilities and integration with Tough Leaders
• Excellent influencing, networking, presentation and communication skills and a proven track record of team cross-functional team working
• Ability to manage multiple projects and adapt priorities according to business and strategic needs
• Comply with highest ethical standards, with a working knowledge of relevant clinical regulations and industry standards as e.g., GCP
• High level of emotional intelligence and motivation, outgoing optimistic personality
• Action Oriented - Pushes self-outside of comfort zone to take action when needed
• Peer Relationships - Professional and respectful in interactions with others at all times
• Drive for Results - Delivers results as it relates to the specific task or situation
• Customer & Externally Focus - Builds good relationships with TLs
• Proactive - Works off own initiative
• High English level
• Computer literacy
• Driving licence

Qué ofrecemos

• Barcelona based
• 20% bonus
• Company car
• Social benefits (health insurance, ticket restaurant, pension plan)