Quick Summary
1. Lead development and execution of medical strategy: 1) Responsible for productive discussion with internal cross-functions including Global/AP,
2-3 years clinical working experience on relevant therapeutic area/or 2-3years working experience on pharmaceutical industry is preferred. Thorough understanding and command of GCP, HCC.
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 jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Responsibilities
~2 min read1. Lead development and execution of medical strategy:
1) Responsible for productive discussion with internal cross-functions including Global/AP, medical insights collection with key national external stakeholders including KOLs etc..
2) Responsible for exhaustive collection of information regarding the latest progress in therapeutic areas/products/competitors, existing knowledge gaps, scientific evidence gaps and clinical practice gaps.
3) Responsible for authoring the Medical Strategy after collection of input and insights from a wide cross-section of internal and external stakeholders.
4) Responsible for directing medical strategy and developing medical projects.
2. Lead clinical study management
1) Ensure the study is designed and operated in compliance with related SOP and other required regulations.
2) Design and compose clinical study protocols as required; submit concept/protocol for internal review and approval; manage the study budget and phasing; ensure the registration of the study online as required; present at investigator meeting if necessary.
3) Set up plan for CSR and publication; review study report; carry out medical monitoring during the clinical study.
4) MAO/CRO collaborations on study operation.
5) Collaborate with Statistician and Data Management team for SAP and data monitoring as required.
6) Ensure the AEs in the study are reported as required.
3. Determine the theme and high-quality medical content of national activities including advisory board and expert discussion; Contribute to the theme of medical educational activities and materials. Closely work with ME/MSL team when necessary.
4. Understand the recent progress in literature/congress in relevant therapeutic areas and products/competitors, HCP perceptions; Generate insights from the above resources, then integrate and share with cross-functional team.
5. Establish good communication and cooperation with internal and external customers, including Global and Regional (AP) MAF, R&D (CD, RA, CDTL et al.), ME, MSL, MKT, Sales, PR, BD, Strategic MKT, MKT Access, CRO etc.
6. Expert review and provision of careful, thoughtful input into the promotional/educational materials and other project-based activity materials from a scientific viewpoint.
7. Provide TA or product related training/support to Marketing/Sales and other departments.
Nice to Have
~1 min readLocation & Eligibility
Listing Details
- First seen
- September 27, 2026
- Last seen
- September 27, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 56%
- Scored at
- September 27, 2026
Signal breakdown
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