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Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
Global exercise reimbursement.
Two weeks off (one of them fully paid) for volunteer work.
As the Asia Pacific Ophthalmology Medical Director, your role will be to develop the AP Medical Strategy and AP Medical Affairs Product Plan for assigned Ophthalmology products in line with Global TA/Disease Area Stronghold and Regional Cross-Functional Therapeutic Area Team(s) (RCFT) strategies, taking into account both weighted needs of the AP countries and feedback from the external scientific communities/thought leaders. You will drive the implementation of the AP Ophthalmology Medical Affairs Plan for assigned products across AP on time and within budget. Your role will also support the Therapautic Area (TA) Lead as required in leading the AP Integrated Value Team (AP IVT) to develop and drive regional TA strategy, ensuring effective communications between the key regional and global groups. Yuo will also represent AP MAF for the assigned Global Medical Affairs Teams (GMAT, CDT ad hoc), on strategic and tactical matters, as delegated by the TA Lead and act as the medical affairs expert and drive a unified Medical AP voice for a specific product or group of products. Responsibilities: AP Medical Affairs Franchise Leadership Act as the AP MAF expert especially for Ophthalmology In partnership with TA Lead, develop and drive the strategy for the TA Articulate the consolidated medical voice for AP for the TA Represent AP voice at regional and global teams for building the TA and brand strategy and provide input into the development plans of the products included in the TA Develop and maintain expertise in products, market trends, competitor activities etc. Build /maintain network with key external thought leaders to ensure clear understanding of external thinking and ensure the Company Medical strategy reflects the external environment Provide scientific leadership for AP cross functional and country MAF teams and ensure regular communication between regional and local MA teams Be accountable for the execution of the AP Medical Plan and budget for regional activities for TA and brands, as delegated by the TA Lead Provide support to the AP Medical TA team to deliver AP MA Strategy and Plan: Collaborate with internal stakeholders to gather input for the AP Medical Affairs Product Plan(s) for designated product(s) Work with the other functions to develop approaches to support successful market access for allocated product(s) in partnership with Health Economics, the CDT (Compound Development Team) and lifecycle management teams Leverage product(s) expertise, medical and market insights to shape and direct implementation of product(s) strategies and plans Ensure effective and regular communications between Global, Regional and local MA teams, including regular communications to help minimise duplication of clinical, advocacy and access programmes across countries, and facilitate co-ordination between AP Medical Affairs, CDT, Strategic Marketing, Health Economics and individual countries Provide Medical and Scientific training for internal and external stakeholders Work with the TA teams in AP to proactively identify and provide medical input into opportunities for new indications or lifecycle extensions for allocated product(s) A member of the relevant Ophthalmology compound GMATs: To represent the unified AP voice for the TA To shape AP MAF Strategy for the TA To ensure timely and reliable input from AP into the Compound Development Team (CDT), including input into phase II/ III designs, and country and site selection for the respective TA To ensure input into the Global Clinical Program with the aim to have representation from appropriate AP countries To provide input on the breakthrough research in line with the unmet medical/social needs in AP region External Relationships To build, maintain and leverage relationships with experts and other important stakeholders related to the activities in the Ophthalmology TA to gain input into the development of the product strategy, to specific protocols, and to services ensuring high-quality disease care. Product Safety and Regulatory Requirements As per the J&J guidance and SOPs: Manage Product-related medical safety issues and provide input to the PV AP Pharmacovigilance & Medical Compliance, Janssen AP Medical Affairs and Global Safety Management Teams (SMTs). Work with Regulatory Affairs & Product Issue Management Team to coordinate and manage product-related Issues and support major quality incidents / recalls throughout Janssen AP Escalate issues and enquiries as appropriate Ensure adequate clinical input is provided to Core Compound Data Sheet or Patient Information by the MAF Director/ advisor update process and where appropriate ensure development and approval of clinical overview. Study Planning and Execution Drive data gap analysis and data generation plan in support of the TA Lead Ensure that all AP MA protocols (Regional AP and single country) are in alignment with, and support, the medical strategy for the TA Act as Study Responsible Physician on regional AP studies and ensure all relevant SOPs are followed Provide scientific support for regional AP studies regarding clinical studies design, statistical plans, CSR, publications as appropriate etc. Review and approve single country concepts (intervention, Real World Evidence, Investigator Initiated Studies etc) in ReCAP Participate as a member of AP Protocol Review Committee for assigned TA products Publications and communications Develop the AP MA publication and communication strategy and plans for assigned TA (as part of the MA Strategy and Plan for allocated product(s), in alignment with the regional and Global publication strategy). Medical Education Develop the Regional AP Medical Education activities for assigned TA as part of the MAF Annual plans for the products in the TA Manage and execute the regional Medical Education strategy and events, including company standalone program, scientific symposia, publications, speaking engagements, webinars, and advisory boards etc. Other Activities as Required Provide input to AP business development initiatives for allocated product(s) when requested Partner with the late lifecycle management group to provide proactive medical input for lifecycle extension opportunities as appropriate Medical review and approval of market research materials Qualifications Medical degree and higher medical qualification or PhD essential 5+ years experience in clinical medicine in an area relevant to the TA 8+ years industry / business experience with a minimum of 3 years experience in a relevant area for this function (e.g. Medical Affairs or Clinical R&D) Working in a matrix system Asia Pacific specificity awareness Excellent knowledge of Ophthalmology with a good knowledge of all products within TA In-depth knowledge and hands-on experience of clinical trial design and study data analysis (e.g. statistical analysis) Good knowledge of Drug development process, MAF specific activities and GCP requirements Awareness of AP Regulatory and reimbursement environment Good knowledge of study execution, pharmacovigilance Sound knowledge of study publication processes and publications Highly customer and market place focused with an Big Picture orientation Innovative with the ability to coordinate and drive a complex and changing environment Ability to work effectively in a matrix environment Strong leadership skills, capable of driving a multi-cultural, virtual team Very strong and demonstrable communication and influencing skills that can impact at a Regional and Global level Awareness of and adherence to Johnson & Johnson Credo values Primary Location Singapore-Singapore-Singapore- Other Locations Asia Pacific-South Korea, Asia Pacific-China-Hong Kong S.A.R., Asia Pacific-Taiwan, Asia Pacific-China, Asia Pacific-Japan Organization Johnson & Johnson Pte. Ltd. (8435) Job Function R&D Requisition ID 2206013888W
Child care benefits
Short term disability