Job Description

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JOB PURPOSE

The Medical Science Liaison (MSL) establishes Takeda\xe2\x80\x99s medical affairs presence with external stakeholders through scientific exchange and research support. This role is the field-based therapeutic area (TA) expert responsible for execution of the TA specific medical plan in the field, predominantly by establishing, developing, and fostering relationships with key external stakeholders. He/she will contribute to the achievement of business success by putting the patient\xe2\x80\x99s needs and safety into primary focus. This position is responsible for executing the medical plan in the field by communicating fair-balanced therapeutic area, product-related and clinical information to external stakeholders (e.g. key opinion leaders (KOLs), physicians, academic institutions, hospital formulary committees) and responding to unsolicited requests for medical information. Additionally, this position will provide key insights learned from the medical and scientific community to internal stakeholders to guide the medical and brand plans. This position will work closely with the Medical Manager in the TA to lead the in-field execution of the TAL/MA-developed medical plan. This position will also collaborate cross-functionally to develop and execute medically relevant strategies and tactics as well as provide scientific expertise and training to cross-functional stakeholders as needed. This position is a field- based position, with approximately 70% time in the field collaborating with KOLs and other external customers as needed. This role will be handling GI, Rare Disease and Neuroscience TA. PRINCIPLE ACCOUNTABILITIES OVERALL

• Lead the in-field execution of the Therapeutic Area (TA) Medical Plan by establishing, developing, and fostering relationships with key external stakeholders
• Support medical strategies for compounds via field-based support from the medical function that are aligned with overall corporate goals and objectives
• Maintain a very high level of knowledge and understanding of the latest scientific/medical knowledge in the relevant therapeutic area by conducting literature searches, analysing clinical papers, attending conferences, courses and other such events
• Provide insights from key external stakeholders to internal cross-functional stakeholders as needed to guide the Brand and Medical Plans

STRATEGIC PLANNING

• Responsible for executing the Therapeutic Area Medical Plan, aligned with both the Brand Plan and the area/regional/ global Medical Plan (where relevant)
• Provide medical/scientific input into the Brand Plan and is a member of the cross-functional Brand Team
• Utilize in-field insights to support medical and scientific strategy and business development
• Identify licensing opportunity and supports due diligence analyses as needed
• Provide field-based support from the medical function that are aligned with overall corporate goals and objectives
• 
  Ensure appropriate and effective external stakeholder management by utilizing objective, aligned scientific criteria to profile KOLs and creates and regularly updates the TA KOL list

CONTRIBUTION TO ORGANIZATION THROUGH MEDICAL EXPERTISE

• Participate in the development and implementation of key medical activities (e.g. Advisory Boards, Focus Group Meetings, medical education and peer-to-peer training activities) as directed by the Therapy Area Lead
• Create or support the development of medical/scientific materials and slide decks as needed (e.g. MSL slide decks and advisory board slides) and ensure the content is appropriately reviewed and approved as per Takeda policies
• Identify educational opportunities that are aligned with Takeda\xe2\x80\x99s medical education strategies
• Provide medical booth and session coverage at scientific meetings and report information of strategic interest to cross-functional internal stakeholders
• Provide clinical presentations and medical information to managed markets, government accounts, and other external stakeholders upon request and as appropriate

CORPORATE GOVERNANCE

• Ensure that all field scientific-medical communications are fair-balanced, based on appropriate scientific evidence, and compliant with local regulatory norms and internal compliance rules
• Ensure compliance of all responsible activities to relevant laws and regulations as well as internal standards and SOPs

• Support the company reputation and profile in the field

EXTERNAL STAKEHOLDER MANAGEMENT

• Establish Takeda\xe2\x80\x99s presence with KOLs and academic institutions in defined geographies for therapeutic areas of strategic interest to the company by identifying, developing, and fostering relationships with KOLs
• Meet regularly with identified KOLs to provide ongoing, balanced scientific exchange related to on-label indications and disease state(s)
• Respond to HCP unsolicited requests for medical information (including off-label information) related for marketed Takeda products and Takeda pipeline products
• Support scientific training of Takeda-contracted speakers by providing ongoing support and education as needed

CROSS-FUNCTIONAL COLLABORATION

• Provide medical insights and intelligence from the field to key cross-functional internal stakeholders within compliance framework to support the development and life-cycle management of Takeda compounds
• Act as field-based reference point of scientific and clinical expertise for cross-functional internal stakeholders (e.g. medical, regulatory, commercial, market access) through training and ad-hoc support
• Serve as an ongoing, infrequent training resource for sales representatives as per requests by commercial or sales Training, utilizing approved training materials

EVIDENCE GENERATION

• Support ongoing/future Company Studies (MACS/CCR and global led Clinical/R&D studies)
• Support the development and implementation of the LOC TA evidence generation plan
• Support unsolicited requests from HCPs for investigator-initiated sponsored research (IISR) proposals by providing appropriate investigator support as per Takeda SOP
• Develop and support national disease registries and RWE projects for relevant disease areas as needed

PATIENT-CENTRICITY

• Provide support and/or leadership in planning and implementation of patient access programs as needed and as per local regulatory requirements
• Prioritize patient safety by following all PV-related processes
• Support reporting of product-related medical safety issues by providing input on product-related quality issues and incidents to the local PV-team

EDUCATION, EXPERIENCE, AND SKILLS Education

• Masters Degree in Life Sciences, Pharmacy or similar discipline

Preferred:

• A Doctoral Degree in Life Sciences (e.g. Ph.D.) or medical post-graduate (e.g. MD) or equivalent

Required experience

• 0-2 years working experience in medical affairs in pharmaceuticals, healthcare industry, or academia

PERSONAL CHARACTERISTICS

• Excellent interpersonal skills with the ability to develop relationships easily, even with challenging people
• Excellent verbal and written communication skills in English; fluency in other languages is a plus
• Excellent oral presentation skills
• Strong planning & organization skills with ability to prioritize
• Independent and self-driven with a positive work ethic
• Proven track record of teamwork, cross-functional collaboration, and leadership
• Results oriented with high sense of urgency and adherence to timelines
• Meticulous and strong analytical skills
• Ability to engender trust and respect of peers and superiors
• High integrity, ethical & professional mindset
• Well versed in highly technical and scientific languages
• Acts with integrity, fairness, honesty, and perseverance (\xe2\x80\x9cTakeda-ism\xe2\x80\x9d)
• Proficiency in Microsoft Office applications including Word, Excel, PowerPoint, and Outlook

TRAVEL REQUIREMENTS

• Ability to drive to or fly to various meetings/client sites

Locations

Selangor, Malaysia

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time