Description
Job Title : PDT Medical Science Liaison (MSL)
Location : Indonesia
About the role :
- 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, analyzing 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 Medical and Brand Plans
How you will contribute :
Strategic Planning
Develop and execute a TA specific MSL scientific engagement plan aligned with the TA Medical Plan to guide field workEnsure appropriate and effective external stakeholder management by utilizing objective, aligned scientific criteria to profile KOLs and creates and regularly updates the TA KOL listCapture and share in-field insights to support brand, medical and scientific strategy and business developmentParticipate as a member of the Brand Team for the assigned TAProvides medical and scientific expertise to commercial partners as needed and within regulatory guidelinesContribution 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 per Medical planCreate 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 policiesIdentify educational opportunities that are aligned with Takeda’s medical education strategiesProvide medical coverage at scientific meetings and report information of strategic interest to cross-functional internal stakeholdersProvide clinical presentations and medical information to managed markets, government accounts, and other external stakeholders upon request and as appropriateCorporate 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 rulesEnsure compliance of all responsible activities to relevant laws and regulations as well as internal standards and SOPsSupport the company reputation and profile in the fieldExternal Stakeholder Management
Establish Takeda’s 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 KOLsMeet 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 productsSupport scientific training of Takeda-contracted speakers by providing ongoing support and education as neededCross-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 compoundsAct 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 supportProvide disease and or clinical medical training to commercial team as needed utilizing approved training materialsClinical Research
Support ongoing / future Company Sponsored Studies (i.e. provides LOC review of proposed CRO site lists, attends site visits, provides site / investigator feedback to clinical operations) following the appropriate requests from Area / Regional or Global clinical developmentSupport unsolicited requests from HCPs for investigator-initiated sponsored research (IISR) proposals by providing appropriate investigator support as per Takeda SOP as well as engaging with Global External Research (GOR) on IISR proposals as appropriateProvide support to Medical Affairs Company Studies (MACS) as needed including site identificationDevelop and support national disease registries and Real World Evidence (RWE) projects for relevant disease areas as neededPatient-Centricity
Provide support and / or leadership in planning and implementation of patient access programs as needed and as per local regulatory requirementsPrioritize patient safety by following all PV-related processesSupport reporting of product-related medical safety issues by providing input on product-related quality issues and incidents to the local PV-teamContinuous Improvement
Responsible for maintaining a very high level of disease and product knowledge through continuous educationAttend courses and industry meetings, reads industry publications and discusses Therapeutic Areas with colleagues to keep up to date with developments within the pharmaceutical industry and pharmaceutical medicinesStructural Organization
Complete all required training, activity documentation, expense reporting, and other administrative responsibilitiesWhat you bring to Takeda :
Education :
Required :Bachelor degree in Life Sciences, Pharmacy or similar discipline, life science or medical science graduates.
Preferred :A medical post-graduate (e.g. MD), Doctoral Degree in Life Sciences (e.g. Ph.D.) or equivalent
Fresh graduate or has working experience in medical affairs in pharmaceuticals, healthcare industry, or academia
Experience
Minimum 1 year prior MSL experience, in relevant Therapeutic AreaProduct launch experienceExperience working in relevant Therapeutic AreaClinical research experienceExcellent interpersonal skills with the ability to develop relationships easily, even with challenging peopleExcellent verbal and written communication skills in English; fluency in other languages is a plusExcellent oral presentation skillsStrong planning & organization skills with ability to prioritizeIndependent and self-driven with a positive work ethicProven track record of teamwork, cross-functional collaboration, and leadershipResults oriented with high sense of urgency and adherence to timelinesMeticulous and strong analytical skillsAbility to engender trust and respect of peers and superiorsHigh integrity, ethical & professional mind setWell versed in highly technical and scientific languagesActs with integrity, fairness, honesty, and perseverance (“Takeda-ism”)Proficiency in Microsoft Office applications including Word, Excel, PowerPoint, and OutlookAs with all Takeda positions, the Medical Science Liaison is expected to conduct themselves in line with the Company culture and Takeda-ismMore about us :
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Empowering our people to shine :
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Jakarta, Indonesia
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
