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Medical Scientific Liaison (MSL) Oncology – Southern Germany - Germany  

Takeda (company)

Posted on : 19 September 2017

Project Description

Medical Scientific Liaison (MSL) Oncology – Southern Germany
Are you looking for a patient-focused, innovation-driven company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Medical Science Liaison (MSL) Oncology – Southern Germany, field-based in Bavaria or Baden-Württemberg.
Takeda is a global pharmaceutical leader with more than 31,000 professionals working together across 70 countries. We have an unwavering dedication to put people first and we live our values of Takeda-ism—Integrity, Fairness, Honesty, and Perseverance. We are united by our 235-year legacy of research-based pharmaceuticals and our mission to strive toward Better Health and a Brighter Future for people worldwide through leading innovation in medicine.
Watch our Medicine for the World video: Watch our Medicine for the World video
Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a MSL Oncology, Southern Germany, working on the German Oncology Medical Affairs team, a typical day will include:
Role Objective
Provide local country field-based support from the medical function in order to achieve the company’s goals
Identify and develop strong, sustainable peer-to-peer relationships with external stakeholders through excellent, best-in-class engagement to support the medical/scientific objectives of the company
Assist with launch of new oncology products in market
Medical/Scientific Affairs
Continuously screen, review and analyse scientific literature; generate summaries & critical assessments if appropriate
Attend local and global congresses to gather information for dissemination to internal stakeholders
Use specific disease and product knowledge to develop Takeda in a given therapeutic area; i.e. answer medical/technical unsolicited enquiries from HCPs, provide accurate and non-promotional scientific information relating to licensed and unlicensed indications following unsolicited requests from HCPs, etc.
Participate in the development and implementation of key medical activities (e.g. Advisory boards, medical education and peer-to-peer training activities)
Provide clinical presentations and medical information as necessary
Participate in development of patient services and healthcare solutions
Insight generation
Identify and develop long term peer-to-peer relationships with opinion leaders and other relevant stakeholders in order to understand their unmet needs and implement a targeted approach and tactics in order to present medical data in the most efficient way
Support Medical Advisors by acting as consultants on data interpretation and real world experience with Brigatinib.
Act as field-based reference points of scientific and clinical expertise for sales force and other internal stakeholders (e.g. Market access) through training and ad-hoc support, in alignment with Takeda project teams
Support advisory boards including development, implementation, and facilitation, as needed
Establish and maintain relationships with KOLs
Assist with all elements of local product launches
Evidence generation
Support ongoing and future Company Sponsored Studies  i.e. provides LOC review of proposed CRO site lists, attendance at Global/Regional Investigator Meetings, attend motivational site visits, provides site/investigator feedback to clinical operations etc. following the appropriate request from Global Development Operations and inform other LOC functions on progress in site involvement process in a timely manner
Capture and share in-field insights to support medical and scientific strategy and business development. Share in-field insights in a compliant manner with relevant business functions.
Facilitate unsolicited requests from HCPs for investigator-initiated sponsored research proposals through engagement with Global External Research
Support Medical Affairs Company Studies (MACS) through site selection, accrual monitoring, and training
Development and support of national disease registries and Real World Evidence (RWE) projects for relevant disease areas. Understand the patient journey leverage points and provide insights to support medical and scientific strategy development
Interact with opinion leaders to communicate and advance Takeda’s scientific platform, as aligned with organisational goals, objectives and medical plans
Ensure consistent communication to external stakeholders of ongoing clinical trial program when requested
Staff Congress booths to reactively provide fair, balanced, and unbiased information regarding products
Assist with the development of internal training material when requested. 

Key Capabilities: 
• More than 2 years of experience as MSL or other relevant Pharma industry experience is preferred
• Targeted lung cancer therapy experience with ALK+ experience (highly preferred) or other targeted therapy experience (e.g. EGFR) within solid tumors is preferred 
• Strong customer engagement skills (e.g. communication, negotiations, presentation etc...) with the ability to engage both external and internal customers
• Experience with new product launches, especially in oncology and/or orphan disease markets 
• The candidate should ideally have both solid and haem experience, but not required 
• Education recommended to be PharmD, MD or PhD

Key areas: 
Bavaria / Bayern 
Keywords: Munich / München, Stuttgart, Nürnberg, Mannheim, Augsburg, Karlsruhe, Regensburg, Ulm, Freiburg