Clinical Research Physician/Scientist - Seoul - Lilly와 관련된 현재 작업
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Clinical Research Associate
5 개월전에
Seoul, 대한민국 IQVIA 풀타임As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™, we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you...
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Application Scientist
3 개월전에
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Seoul, 대한민국 Boston Scientific 풀타임Title: (Sr) Professional Sales Rep., Cardiac Rhythm Management An exciting opportunity Boston Scientific’s Cardiac Rhythm Management offers a variety of implantable defibrillators and pacemakers to irregular heart rhythms and heart failure and to protect against sudden cardiac death. The company manufactures the world’s first ICD and only...
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Clinical Trial Assistance
5 개월전에
Seoul, 대한민국 IQVIA 풀타임Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...
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Clinical Medical Manager
5 개월전에
Seoul, 대한민국 Novo Nordisk 풀타임Are you passionate about clinical trials and making a difference in the field of healthcare? Do you have expertise in New Therapy Areas such as Cardiovascular disease, Chronic Kidney Disease, Liver Disease, inflammation, Alzheimer’s disease, and emerging therapy areas? We are looking for a Clinical Medical Manager to join our team at Novo Nordisk. Apply...
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Seoul, 대한민국 Boston Scientific 풀타임Title: (Sr) Professional Sales Rep., Cardiac Rhythm Management An exciting opportunity Boston Scientific’s Cardiac Rhythm Management offers a variety of implantable defibrillators and pacemakers to irregular heart rhythms and heart failure and to protect against sudden cardiac death. The company manufactures the world’s first ICD and only S-ICD...
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Seoul, 대한민국 Boston Scientific 풀타임An exciting opportunity Boston Scientific Interventional Cardiology team is looking for high energy, driven, passionate talent. This role also entails a good understanding of the catheterization lab and fostering strong relationships with physicians and staffs. In Interventional Cardiology (IC) we design, develop, and produce technologies for...
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Seoul, 대한민국 Novo Nordisk 풀타임Are you passionate about driving clinical trials and providing medical expertise? Are you a seasoned medical professional with expertise in clinical trials and therapy areas such as Cardiovascular disease, Chronic Kidney Disease, Liver Disease, inflammation, Alzheimer’s disease, and emerging therapy areas? If so, we have an exciting opportunity for you...
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Seoul, 대한민국 IQVIA 풀타임Job Overview Serve as Data Operations Coordinator (DOC) Essential Functions • Manage delivery of projects through full data management study life-cycle (with minimal guidance). • With guidance from DTL or Manager, manage project timelines and quality. • Determine resource needs. • Identify out-of-scope work. • Serve as Data Operations...
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Seoul, 대한민국 Boston Scientific 풀타임Title: (Sr) Professional Sales Rep., Peripheral Intervention An exciting opportunity Over 200M patients around the world suffer from Peripheral Arterial Disease (PAD) with less than 1% receiving an intervention. We’ve built a strong portfolio of products to serve this market and are uniquely positioned to provide physicians and hospital systems...
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Seoul, 대한민국 Boston Scientific 풀타임Title: Marketing Manager, PI & IO An exciting opportunity We look for marketers who are business leaders who will shape our business strategy and champion new ways to address unmet customer needs. The Peripheral Interventions (PI) & Interventional Oncology (IO) team is dedicated to bringing new and innovative products to market that help improve outcomes...
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Seoul, 대한민국 Philips 풀타임JOB DESCRIPTION Job Title Clinical Application Specialist - Ultrasound Job Description Company Introduction 필립스코리아는 1976년 한국 법인을 설립한 후, 지난 40년간 헬스케어, 소비자 라이프스타일, 조명 등 3대 사업 부문을 중심으로 한국 소비자에게 의미 있는 혁신을 제공하고 한국의...
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Seoul, 대한민국 Intuitive Surgical 풀타임Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team,...
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Data Scientist
1개월전에
Seoul, South Korea Coupang 풀타임[회사 소개] CFS CFS (Coupang Fulfillment Services)는 쿠팡의 물류를 총괄하는 쿠팡의 계열사입니다. CFS는 물류센터 또는 FC(Fulfillment Center) 운영을 책임지고 있으며, 업무 효율성과 전문성 제고를 통해 글로벌 이커머스 기업으로 성장하기 위한 혁신을 이끌어 가고 있습니다.쿠팡의...
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Seoul, 대한민국 MEDPACE 풀타임Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...
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Seoul, 대한민국 Barco 풀타임Barco seeks a Business Development Manager to drive sales growth in the Diagnostic Imaging business segment by effectively communicating with End Users, Key Opinion Leaders, and Partners to generate demand and ensure that the company's clinical, operational, and financial solution advantages are clearly understood. Key Responsibilities: Enhance brand...
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Seoul, 대한민국 Boston Scientific 풀타임Title: (Sr) Professional Sales Rep., PI & IO An exciting opportunity Over 200M patients around the world suffer from Peripheral Arterial Disease (PAD) with less than 1% receiving an intervention. We’ve built a strong portfolio of products to serve this market and are uniquely positioned to provide physicians and hospital systems with a full tool box of...
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Seoul, 대한민국 Amazon Web Services Korea LLC - D54 풀타임Are you looking to work at the forefront of Machine Learning and AI? Would you be excited to apply cutting edge Generative AI algorithms to solve real world problems with significant impact? The Generative AI Innovation Center at AWS is a new strategic team that helps AWS customers implement Generative AI solutions and realize transformational business...
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CFS Data Scientist
1개월전에
Seoul, 대한민국 Coupang 풀타임[회사 소개] CFSCFS (Coupang Fulfillment Services)는 쿠팡의 물류를 총괄하는 쿠팡의 계열사입니다. CFS는 물류센터 또는 FC(Fulfillment Center) 운영을 책임지고 있으며, 업무 효율성과 전문성 제고를 통해 글로벌 이커머스 기업으로 성장하기 위한 혁신을 이끌어 가고 있습니다.쿠팡의...
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Seoul, 대한민국 Boston Scientific 풀타임Title: (Sr.) Professional Sales Rep., TAVI Location: Busan & Daegu Transform Lives with Cutting-Edge SolutionsTranscatheter Aortic Valve Implantation (TAVI) is now the gold standard for treating patients with severe aortic stenosis, proven to be both safe and highly effective. Since 2022, the Korean government has expanded reimbursement coverage for both...
Clinical Research Physician/Scientist
2 개월전에
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
The primary responsibility of the Business Unit - Medical Affairs CRP/CRS is to provide expert medical support to all aspects of the local business, to ultimately enhance the customers' experience in interacting with the company. This includes local marketed product support (participate in the development of the "patient journey" and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for New and Supplemental New Drug Submissions and participating and presenting at meetings with government regulatory agencies), medical support for pricing, reimbursement and access(PRA) (providing medical guidance on the PRA plan and interacting with government PRA agencies as needed), and leading in local scientific data dissemination (leading and presenting at conferences, advisory boards, etc., and overseeing the development of the scientific content of educational programs). These responsibilities are generally related to late phase and marketed compounds, but can also include early phase trials (for example, phase I and II trials). The CRP/CRS is responsible for collaborating with the global teams in the planning, startup and conduct of phase 3b/4 studies (and phase I and II studies where applicable), as well as non clinical trial solutions/activities that are conducted in affiliates/countries as described in the clinical plan. The core job responsibilities may include those listed below as deemed appropriate by line management, as well as all other duties as assigned.
Business/ customer support (core and post launch support)
Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health care providers)
Actively address customer (payer, patient and health care providers) questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts.
Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global Patient Outcomes/Real World Evidence and global PRA, clinical management or personnel and other cross-functional management during the development of the local business plan.
Contribute as a scientific and medical expert to activities and deliverables of the PRA organization, in particular giving clinical input and insight to develop payer partnership programs and defend the product value.
Support business-to-business and business-to-government activities as medical expert.
Contribute actively on an ongoing basis to the strategic planning for currently marketed brands.
By offering scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team.
Support training of sales representatives, and other medical representatives.
Become familiar with market archetypes and potential influence on the medical interventions for the product.
Take a leadership role in defining the Patient Journey and corresponding Moments of Truth based on his/her medical knowledge. Become patient advocate, as well as a medical expert.
Understand and apply knowledge of customer insights to all customer-related activities.
Provide medical insight and training to patient support programs (for example, Diabetes Nurse Educators Service).
Participate in local or national trade associations, as appropriate.
Scientific Data Dissemination/Exchange
Knowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals.
Understand and actively address the unsolicited scientific information needs of external health care professionals according to guidelines above.
Support the planning of symposia, advisory board meetings, and and/or the facilitation of other meetings with health care professionals.
Support medical information associates in preparation and review of medical letters and other medical information materials.
Support training of local medical personnel, including medical and/or outcome liaisons and health outcomes staff.
Prepare or review scientific information in response to customer questions or media requests.
Provide follow-up to information requested by health care professionals as per global SOPs.
Support data analysis and the development of slide sets (through reviewing and/or approving) and publications (abstracts, posters, manuscripts).
Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community on a local, national, regional, and possibly international basis.
Develop and maintain appropriate collaborations and relationships with relevant professional societies.
Support the design of customer research as medical expert.
Provide congress support (for example, availability to answer questions at exhibits, provide oral and poster presentations, staff medical booth, meet thought leaders, and participate in customer events).
Participate in data analyses, development of scientific data dissemination, and preparation of final reports and publications.
Participate in reporting of clinical trial data in Clinical Trial Registry activities.
Clinical Planning
Communicate and collaborate with Director-Medical and Business Unit Team Physician/Regional Medical Leader as needed to ensure life cycle plans for drugs in development address customer needs or communicate and collaborate such needs as delegated by Director-Medical and Business Unit Team Physician/Regional Medical Leader, as needed, global Medical Affairs and Development teams, Global Patient Outcomes/Real World Experience, PRA, Therapeutic Area Program Phase, and Early Phase /EPM/Translational Medicine teams.
Communicate local/regional research needs and collaborate with other regions and the global Development and Medical Affairs teams, Global Patient Outcomes/Real World Experience, and PRA teams to ensure Phase 3, 3b, and 4 (and Phase I and II where applicable) clinical programs meet the needs of local/regional customers (for example, through global medical planning processes).
Understand and keep updated with the pre-clinical and clinical data relevant to the molecule.
Represent the clinical needs of the country/region to the business unit medical leadership in the development of clinical strategies, development plans and study protocol design.
Clinical Research/Trial Execution and Support
Review and approve local informed consent documents and risk profiles to ensure appropriate communication of risk to study subjects.
Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review interactions).
Collaborate with regional clinical operations staff, statisticians, health outcomes, research scientists and selected investigators in the development of protocols and data collection requirements.
Participate in investigator identification and selection, in conjunction with clinical teams.
Ensure that the clinical operations team has documented the completion of administrative requirements for study initiation and conduct (i.e., ethical review board, informed consent, regulatory approval/notification) consistent with Good Clinical Practices (GCPs) and local laws and requirements.
Assist in the planning process and participate in study start-up meetings and other activities to provide the appropriate scientific training and information to investigators and site personnel.
Serve as resource to clinical research site monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study.
Review IIT proposals and publications, as requested
Contribute to global alignment of Phase 3b/4 clinical studies (and Phase I and II studies where applicable) planned by country (ies) or global Development team.
Understand and actively address the scientific information needs of all investigators and personnel.
Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with corporate patient safety policies and procedures.
Regulatory Support Activities
Participate in development and review of local labeling and labeling modifications in collaboration with global Development, brand teams, regulatory, and legal. Demonstrate deep knowledge of local label.
Provide medical expertise to regulatory scientists.
Support/ assist in the preparation of regulatory reports, preparation for regulatory agency advisory committee hearings and label discussions, local registration efforts, and communication and resolution of regulatory issues, including regulatory response, from an affiliate/country perspective.
Participate in advisory committees.
Participate in risk management planning along with global Development team(s), business unit, local area, and Global Patient Safety (GPS).
Scientific I Technical Expertise and continued development
Be aware of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the product, both near term (1-2 years) and longer-term (3-5 years).
Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and keep updated with medical and other scientific developments relevant to the product.
Responsible for the scientific training of the clinical study team.
Acts as scientific consultant and protocol expert for clinical study team members and others in medical.
Explore and take advantage of opportunities for extramural scientific experiences.
Attend, contribute and participate in medical congresses/scientific symposia.
General Responsibilities
Support the business unit management team, including medical leadership in preparation and administration of the local or business unit medical budget.
Actively set and meet individual professional development goals and contribute to the development of others by being an active source of coaching and feedback to co-workers, and direct reports as applicable.
Collaborate proactively and productively with all alliance, business, and vendor partners.
Participates in active coaching by providing timely and constructive feedback to co-workers, others on the clinical medical team, in the spirit of development, increased team effectiveness and cohesiveness.
As applicable, works closely with direct reports on performance management plans (objectives), development plans, and documentation of their expertise. Keeps these documents and plans up to date. Meets regularly with each direct report to coach, mentor, evaluate performance, evaluate training and development needs, and monitor career development goals. Maximizes each individual direct report's career potential, maximizing the value to the organization.
Actively participate in recruitment, diversity, and retention efforts, and hiring efforts as applicable.
Participate in committees, Six Sigma initiatives and task forces as requested by business unit/corporate management.
Model the leadership behaviors.
Be an ambassador of both patients and the Lilly Brand.
Launch Support
Key skills/requirements:
Needs deep knowledge of molecule and existing development plan
Will need to be well versed on trial(s) results and conclusions, thus will need to work closely with submission teams
Ideally would be partnered with an affiliate headcount sitting within the team who can go back to the region to establish the medical brand team prior to launch - seed the region with experience
Thought leader engagement and relationships will be essential - shared and coordinated responsibility between Global Product Team (GPT) and regions and functions
Works cross-functionally and cross geography
Need strong scientific expertise and people skills
Must have an understanding of the oncology customer, oncology business, with strong planning and execution skills
Staffing will need to be complimented with writing, and additional medical support that will have increasing demand over time
Key responsibilities:
Be a single point of contact for the overall molecule medical affairs within the GBD with the leadership in initially key priority areas: Scientific Platform/Communications Strategy/SOD 3b/4 studies and their supportive study plans Training and education Internal (molecule, MOA, disease state ) External (Disease State) Global Thought Leader plans - in close collaboration with regions and affiliates
Leading all global medical affairs pre- peri- and post launch activities
Leading medical peers (primarily through regional medical point of contact for the product: EU, USMD, EMMBU, Japan) and cross functional collaboration globally within area of all key medical affairs deliverables for the product
Be a voice of GPT medical affairs to the regions and at the same time bring the inputs from the affiliates back to GPT.
Leverage deep product knowledge and educate the network of regional and affiliate peers, so they are ready to support their local launches.
Drive cross tumor shared learnings.
Work collaboratively with Global Tumor team Leads and Global Marketing teams to ensure robust Brand planning.
Core member of the compound safety team
MINIMUM QUALIFICATION REQUIREMENTS:
Medical Doctor. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring.
Knowledge Knowledge of drug development process relevant to country/region preferred
Demonstrated ability to balance scientific priorities with business priorities
Demonstrated strong communication, interpersonal, teamwork, organizational and negotiation skills
Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment.
Ability to engage in domestic and international travel to the degree appropriate to support the business of the team.
Fluent in English, verbal and written communication.
If candidate for a CRS:
An advanced health/medical/scientific (for example, in Pharmacology, physiology, microbiology) or related graduate degree such as DVM, PharmD, PhD and one of following: 1. 3-5 years of clinical experience or 2. more than 5 years of pharmaceutical experience
If experience is either in 1 and or 2 only (for example, no clinical experience), the following must be provided as supporting evidence of candidate’s ability/capability to perform in a CRS role: Clear evidence and documentation of candidate’s direct role and contribution to medical content. This should include evidence of candidate as medical content owner (oversight of content development-creator/creation, reviewer, and approver. Medical content = medical, scientific or clinical information)
Candidate’s selection for CRS role must be endorsed by the BU Med affairs/development VP or equivalent area Senior leadership
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