Medical Scientific Liaison

** STRATEGIC PLANNING**

1. Develop and execute MSL scientific engagement plan aligned with the TA Medical Plan.

2. 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.

3. Capture and share in-field insights to support brand, medical and scientific strategy, and business development.

4. Participate as a member of the Brand Team for the assigned TA.

**CONTRIBUTION TO ORGANIZATION THROUGH MEDICAL EXPERTISE**

1. 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)

2. 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.

3. Identify educational opportunities that are aligned with Takeda’s medical education strategies.

4. Provide medical booth and session coverage at scientific meetings and report information of strategic interest to cross-functional internal stakeholders.

5. Provide clinical presentations and medical information to managed markets, government accounts, and other external stakeholders upon request and as appropriate.

**EXTERNAL STAKEHOLDER MANAGEMENT**

1. 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 KOLs.

2. Meet regularly with identified KOLs to provide ongoing, balanced scientific exchange related to on-label indications and disease state(s)

3. Respond to HCP unsolicited requests for medical information (including off-label information) related for marketed Takeda products and Takeda pipeline products.

4. Support scientific training of Takeda-contracted speakers by providing ongoing support and education as needed.

**CROSS-FUNCTIONAL COLLABORATION**

1. 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.

2. 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

3. Serve as an ongoing, infrequent training resource for sales representatives as per requests by commercial or sales Training, utilizing approved training materials.

4. Support related cross-functional team in planning and implementing disease awareness and patient access programs as needed and as per local regulatory requirements for products within Therapeutic Area.

5. Prioritize patient safety by following all PV-related processes, and support reporting of product-related medical safety issues by providing input on product-related quality issues and incidents to the local PV-team.

**CORPORATE GOVERNANCE**

1. Complete all required training, activity documentation, expense reporting, and other administrative responsibilities.

2. 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.

3. Ensure compliance of all responsible activities to relevant laws and regulations as well as internal standards and SOPs

4. Support the company reputation and profile in the field.

**CONTINUOUS IMPROVEMENT**

1. Responsible for maintaining a very high level of disease and product knowledge through continuous education

**Locations**:
Bangkok, Thailand

**Worker Type**:
Employee

**Worker Sub-Type**:
Regular

**Time Type**:
Full time