Medical Affairs Manager - IBD

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.

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Affairs – Marketed Products

Job Category:

Scientific/Technology

All Job Posting Locations:

Beijing, China

Job Description:

POSITION SUMMARY

Develop medical strategy and medical projects, including clinical study design & operation; determination of the theme & high-quality medical content of national activities and expert discussion, collaboration for medical educational activities; understanding recent progress in relevant therapeutic areas & products/competitors and sharing with cross-functions; communication and collaboration with internal and external customers; expert review and providing scientific input into the promotional/educational/project-based materials; providing TA or product related training/support.

RESPONSIBILITIES may include but no limited to

• Development and execution of medical strategy:

• Responsible for productive discussion with internal cross-functions including Global/AP, medical insights collection with key national external stakeholders including KOLs etc..
• 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.
• Responsible for authoring the Medical Strategy after collection of input and insights from a wide cross-section of internal and external stakeholders.
• Responsible for directing medical strategy and developing medical projects.

• Clinical study management

• Ensure the study is designed and operated in compliance with related SOP and other required regulations.
• 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.
• Set plan for CSR and publication; review study report; carry out medical monitoring during the clinical study.
• MAO/CRO collaborations on study operation.
• Collaborate with Statistician and Data Management team for SAP and data monitoring as required.
• Ensure the AEs in the study are reported as required.

• 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.

• 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.

• 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.

• Expert review and provision of careful, thoughtful input into the promotional/educational materials and other project-based activity materials from a scientific viewpoint.

• Provide TA or product related training/support to Marketing/Sales and other departments.

COMPETENCIES/SKILLS/REQUIREMENTS

• 2-3 years clinical working experience on relevant therapeutic area/or 1-2 years working experience on pharmaceutical industry is preferred.

• Thorough understanding and command of GCP, HCC.
• Good command of English, fluent at reading, writing, speaking and listening.
• Thorough understanding and command of product and relevant therapeutic area knowledge.
• Agile strategic thinking with the development of medical strategy/projects based on unmet needs and aligned with cross-functions.
• Identify data gaps, and collaborate with internal/external stakeholders for study design/operation/publication to meet the gap.
• Implement scientific communication with evidence-based medical content/information via multiple ways.
• Establish trust relationship and collaboration with cross functions, with aligned strategy/responsibilities, providing valued scientific suggestions for the high-quality output.
• Develop action plan for insight collection and KOL engagement based on medical strategy, establish and maintain collaboration with external customers.

OTHERS

• Domestic and International travels are required.

• 试用期内按照公司要求完成入职培训、合规培训及考核并达到相关要求（该等条件和要求属于员工应满足的录用条件，如未能按照公司要求完成相关测试、培训并满足考核，将视为试用期内不符合录用条件。）

Required Skills:

Preferred Skills:

Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Critical Thinking, Cross-Functional Collaboration, Healthcare Trends, Leverages Information, Medical Affairs, Medical Communications, Medical Compliance, Organizing, Product Strategies, Scientific Communications, Strategic Thinking, Tactical Planning