Overview: This position is accountable for leading in the development of clinical evidence generation and dissemination strategies across assigned projects. Main responsibilities and duties: • Lead to evidence generation strategy with collaboration relationships with all cross-functional partners
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Job Overview Support the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department, primarily in one geography. May be required to assist with providing staffing support to assigned
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than
JOB DESCRIPTION: Job Description 1. Quality/Safety: Demonstrate an understanding of the application of the Quality Policy through daily activities. 2. Maintain vigilance to ensure adherence to the Quality Policy and system procedures by promptly reporting non-compliance
Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core
Job Overview Support the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department, primarily in one geography. May be required to assist with providing staffing support to assigned
企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Position Overview: The Sales representative (qPCR) role at Thermo Fisher Scientific Inc. offers an outstanding opportunity to drive significant impact in the biotechnology sector. Based in Seoul, you will
Job Description Summary Job Purpose: The SSO Associate Clinical Project Manager (aCPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development
This is what you will do: The Medical Affairs Associate Medical Lead prepares a medical plan, which serves as the basis of medical activities of Alexion Pharma GK (AP-J) as a whole, and carries it out
■ 職務内容 / Job Description Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Career Category Clinical Job Description Purpose: Provide clinical site contracting services to clinical study teams to support study start up and conduct activities Context: Amgen K.K. office Reports to CTOM (Clinical Trial Oversight Manager) Responsibilities Manage end to end process for
ジェンマブは、革新的で独自性のある抗体治療薬の開発に注力し、患者さんの人生をより豊かにすることを目的としています。 The Role Japan Clinical Pharmacology Lead will serve as the pre-clinical and clinical pharmacology lead on a number of pre-clinical and clinical development programs providing quantitative sciences support and execution of Japan clinical development plans that include characterization and prediction of pharmacokinetics
Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients. Acts as a field-based expert, building relationships with External Experts as trusted scientific partners.
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
Job Description Summary The Study Leader is the leader of the cross-functional clinical trial team (CTT), guides planning andmanagement of the assigned clinical study/studies end-to-end to achieve Global Program Team(GPT), Global Clinical Team (GOT) and GCO objectives. Accountable for
