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포지션 상세
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.
• Develop individual plans and objectives aligned with Medical Affairs Strategy and track progress using the iMedical CRM.
• Integrate scientific data into real-life practice, anticipate responses of different individuals and teams, and generate and share meaningful medical insights during interactions with KIs.
• Execute proactive and reactive outreach plans as approved through the legal/HCC exceptions process.
• Plan and execute external medical activities, including representing and supporting scientific meetings such as congresses, symposia, advisory boards, and investigator meetings.
• Interpret findings and report them with recommendations for action to relevant internal partners.
• Leverage knowledge of standards of care, Janssen company-sponsored clinical trials, investigator-initiated studies, and the competitive landscape to facilitate external-internal research communication.
• Address and manage Investigator-initiated studies upon external requests.
• Engage with external investigators regarding unsolicited research inquiries and act as liaison to Clinical research team (GCO and PADU).
• Provide clinical trial support to identify potential sites, resolve issues with enrolled sites, and participate in meetings such as site initiation visits and investigator meetings.
• Collect and provide meaningful medical insights back to the medical and cross-functional organizations to support strategy development.
• Support initial and ongoing medical/scientific area and product-specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Medical Affairs, GCO/PADU).
• At least 5 years' experience in professional working environment in pharmaceutical or related industries is required.
• Understanding of local regulatory policy and industry's code of practice related to drug registration, pharmaceutical promotion and clinical study.
• Knowledge of scientific and therapeutic principles, with strengths in research and interpretation of scientific publications.
• Expertise in research methodologies, clinical trial design, and related processes.
• Excellent English language skills, spoken and written.
• Interpersonal and communication skills to effectively interact with a broad range of external and internal personnel.
• Must be familiar with Microsoft Word, Excel, and PowerPoint.
• Awareness of, and adherence to, Johnson & Johnson Credo values and International Health Care Business Integrity Guide.
• Domestic and international travel is required.
주요업무
• Develop and maintain external relationships with key Individuals (KIs) to identify scientific needs and stay abreast of current scientific trends, including balanced communication, clinical support, and responding to unsolicited requests for scientific information.• Develop individual plans and objectives aligned with Medical Affairs Strategy and track progress using the iMedical CRM.
• Integrate scientific data into real-life practice, anticipate responses of different individuals and teams, and generate and share meaningful medical insights during interactions with KIs.
• Execute proactive and reactive outreach plans as approved through the legal/HCC exceptions process.
• Plan and execute external medical activities, including representing and supporting scientific meetings such as congresses, symposia, advisory boards, and investigator meetings.
• Interpret findings and report them with recommendations for action to relevant internal partners.
• Leverage knowledge of standards of care, Janssen company-sponsored clinical trials, investigator-initiated studies, and the competitive landscape to facilitate external-internal research communication.
• Address and manage Investigator-initiated studies upon external requests.
• Engage with external investigators regarding unsolicited research inquiries and act as liaison to Clinical research team (GCO and PADU).
• Provide clinical trial support to identify potential sites, resolve issues with enrolled sites, and participate in meetings such as site initiation visits and investigator meetings.
• Collect and provide meaningful medical insights back to the medical and cross-functional organizations to support strategy development.
• Support initial and ongoing medical/scientific area and product-specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Medical Affairs, GCO/PADU).
자격요건
• Relevant science background (e.g., medicine, pharmacy, life science, etc.)• At least 5 years' experience in professional working environment in pharmaceutical or related industries is required.
• Understanding of local regulatory policy and industry's code of practice related to drug registration, pharmaceutical promotion and clinical study.
• Knowledge of scientific and therapeutic principles, with strengths in research and interpretation of scientific publications.
• Expertise in research methodologies, clinical trial design, and related processes.
• Excellent English language skills, spoken and written.
• Interpersonal and communication skills to effectively interact with a broad range of external and internal personnel.
• Must be familiar with Microsoft Word, Excel, and PowerPoint.
• Awareness of, and adherence to, Johnson & Johnson Credo values and International Health Care Business Integrity Guide.
• Domestic and international travel is required.
