[Innovative Medicine] Sr. RWE Specialist (Contractor)

Posted:
1/12/2026, 8:47:58 AM

Location(s):
Seoul, South Korea ⋅ Seoul, Seoul, South Korea

Experience Level(s):
Senior

Field(s):
Medical, Clinical & Veterinary

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Science Liaison

Job Category:

Scientific/Technology

All Job Posting Locations:

Seoul, Korea, Republic of

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

* Own and lead real-world evidence (RWE) studies across the full study lifecycle—from planning and design through execution, analysis, and completion—providing epidemiological and/or statistical leadership in close collaboration with Therapeutic Areas (TAs).

  • Driving study concept development, design, and protocol development using diverse real-world data sources, including prospective and retrospective observational studies, registries, secondary databases (e.g., claims and EMR), and post-hoc analyses of clinical study data.

  • Ensuring appropriate methodological rigor, scientific validity, and overall quality of study design, analysis, and interpretation.

  • Overseeing statistical analysis plans and guiding analytical approaches.

  • Leading the interpretation and discussion of study results.

  • Driving the completion of study reports and peer-reviewed publications.

* Support post-marketing commitment (PMC) studies by providing epidemiological and statistical expertise throughout study planning, design, implementation, and completion, in close collaboration with TAs and cross functional stakeholders.

  • Provide methodological and statistical input to study design and analysis.

  • Participate in cross-functional discussions to ensure regulatory and scientific requirements are appropriately addressed.

  • Review statistical analysis plans and analytical outputs and provide expert feedback as needed.

* Communicate generated evidence through internal and external presentations and publications.

 

  • Master's degree or higher in pharmacy or epidemiology or biostatistics.
  • At least 2-3 years of experience in clinical study design, statistical analysis, and scientific writing study (protocols/analysis plans/results/manuscripts) for evidence generation.
  • Ability to communicate complex analytical concepts and results to non-technical stakeholders.
  • Strong analytical mindset with intellectual curiosity and a collaborative, proactive attitude.
  • Demonstrated experience contributing to publications in international peer-reviewed journals is preferred.
  • Hands-on experience with statistical programming (e.g., SAS and/or R) is a plus.

#LI-Hybrid

Legal Entity

Innovative Medicine(Formerly Janssen)

Job Type

Fixed Term (1 year)

Application Documents

Free-form resume AND cover letter is required (in Korean or English).

Application Deadline

Open until the position is filled.

Notes

  • Preference will be given to individuals subject to national veterans’ benefits and persons with disabilities upon submission of relevant documents as per applicable laws.

  • Only candidates who pass the resume screening will be notified individually. However, notifications may be delayed due to company circumstances.

  • If any false information is found in the application documents, the hiring may be canceled even after the offer is confirmed, and future applications may be restricted.

  • Submitted documents will not be returned and will be deleted upon request.

 

 

Required Skills:

 

 

Preferred Skills:

Analytical Reasoning, Analytics Dashboards, Clinical Trials, Coaching, Collaborating, Communication, Data Reporting, Detail-Oriented, Digital Culture, Digital Literacy, Market Research, Medical Affairs, Medical Communications, Medical Compliance, Product Knowledge, Scientific Research, Stakeholder Engagement, Technical Credibility, Technologically Savvy