Senior BD In-license Specialist
Division
BUSINESS DEVELOPMENT
Job group
IN-LICENSING
Job
IN-LICENSING
Experience Level
Experienced 5 years or more
Job Types
Full-time
Locations
알보젠코리아대한민국 서울특별시 서초구 서초대로 411, GT TOWER 5층

[Responsibilities]

1. Strategic ​Portfolio ​Management ​& Market ​Foresight

  • Proactively analyze global and ​domestic ​pharmaceutical market ​dynamics, competitive landscapes, ​pipeline developments, ​and ​regulatory trends ​to ​shape ​a winning and ​sustainable ​portfolio strategy
  • Generate actionable ​insights ​and ​forward-looking recommendations by ​integrating market ​intelligence, ​financial considerations, ​resource availability, ​and ​strategic fit.


2. Opportunity ​Assessment & ​Product Value Creation

  • Systematically evaluate in-licensing opportunities and internally developed assets, including value‑added generics and 505(b)(2) programs, by assessing clinical differentiation, unmet medical needs, life cycle potential, and competitive positioning.
  • Analyze clinical data, development pathways, and fundamental patent/IP landscapes to identify and articulate product value and risk by cooperating with relevant team.
  • Ensure portfolio assets are positioned for successful development and launch, defining optimal indications, differentiation strategies, and value propositions.


3. Portfolio Prioritization & Governance

  • Lead portfolio prioritization and trade-off decisions across pipeline stages by developing robust business cases and scenario analyses. Facilitate data-driven decision-making balancing strategic objectives, customer and patient insights, development feasibility, and organizational resource constraints.


4. Development & Launch Strategy Excellence

  • Drive and support ongoing and new business development initiatives, including global and regional in-licensing, co-development, and strategic partnerships.
  • Oversee launch readiness planning to ensure activities are executed in the right sequence, on time, and at the required quality level


5. Portfolio Visibility & Performance Monitoring

  • Develop and maintain portfolio management tools, dashboards, and reporting systems to provide transparent, real-time visibility of pipeline status, risks, and milestones.
  • Communicate portfolio road maps clearly across functions to ensure shared understanding and alignment


[Qualifications]

1. Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline

2. Minimum 5 years of experience in Business Development, Licensing, Portfolio, or Strategy within the pharmaceutical or biotech industry

3. Proven experience in in‑licensing transactions and evaluation of internal and external product

opportunities

4. Strong understanding or hands‑on experience with development of generics, complex generics, and/or value‑added 505(b)(2) products

5. Ability to assess clinical development pathways and interpret fundamental patent and IP landscapes to identify product value

6. Solid capability in market, competitor, and pipeline analysis across domestic (Korea)

and global markets

7. Experience preparing business cases, opportunity assessments, and internal approval

materials

8. Demonstrated ability to work effectively with cross‑functional teams (Regulatory, Commercial, Finance, Manufacturing, SCM)

9. Strong communication skills in Korean and English, with experience interacting with global partners

10. High level of ownership and analytical mindset preferred

Share
Senior BD In-license Specialist

[Responsibilities]

1. Strategic ​Portfolio ​Management ​& Market ​Foresight

  • Proactively analyze global and ​domestic ​pharmaceutical market ​dynamics, competitive landscapes, ​pipeline developments, ​and ​regulatory trends ​to ​shape ​a winning and ​sustainable ​portfolio strategy
  • Generate actionable ​insights ​and ​forward-looking recommendations by ​integrating market ​intelligence, ​financial considerations, ​resource availability, ​and ​strategic fit.


2. Opportunity ​Assessment & ​Product Value Creation

  • Systematically evaluate in-licensing opportunities and internally developed assets, including value‑added generics and 505(b)(2) programs, by assessing clinical differentiation, unmet medical needs, life cycle potential, and competitive positioning.
  • Analyze clinical data, development pathways, and fundamental patent/IP landscapes to identify and articulate product value and risk by cooperating with relevant team.
  • Ensure portfolio assets are positioned for successful development and launch, defining optimal indications, differentiation strategies, and value propositions.


3. Portfolio Prioritization & Governance

  • Lead portfolio prioritization and trade-off decisions across pipeline stages by developing robust business cases and scenario analyses. Facilitate data-driven decision-making balancing strategic objectives, customer and patient insights, development feasibility, and organizational resource constraints.


4. Development & Launch Strategy Excellence

  • Drive and support ongoing and new business development initiatives, including global and regional in-licensing, co-development, and strategic partnerships.
  • Oversee launch readiness planning to ensure activities are executed in the right sequence, on time, and at the required quality level


5. Portfolio Visibility & Performance Monitoring

  • Develop and maintain portfolio management tools, dashboards, and reporting systems to provide transparent, real-time visibility of pipeline status, risks, and milestones.
  • Communicate portfolio road maps clearly across functions to ensure shared understanding and alignment


[Qualifications]

1. Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline

2. Minimum 5 years of experience in Business Development, Licensing, Portfolio, or Strategy within the pharmaceutical or biotech industry

3. Proven experience in in‑licensing transactions and evaluation of internal and external product

opportunities

4. Strong understanding or hands‑on experience with development of generics, complex generics, and/or value‑added 505(b)(2) products

5. Ability to assess clinical development pathways and interpret fundamental patent and IP landscapes to identify product value

6. Solid capability in market, competitor, and pipeline analysis across domestic (Korea)

and global markets

7. Experience preparing business cases, opportunity assessments, and internal approval

materials

8. Demonstrated ability to work effectively with cross‑functional teams (Regulatory, Commercial, Finance, Manufacturing, SCM)

9. Strong communication skills in Korean and English, with experience interacting with global partners

10. High level of ownership and analytical mindset preferred