Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across
Job Description About This Role: We are seeking a highly skilled and experienced Manager, Drug Safety to join our team in Tokyo, Japan. In this critical role, you will lead our drug safety and pharmacovigilance efforts,
General Information Job Advert Title: Clinical Trial Associate (CTA) Location: Tokyo HQ (Nihonbashi) Division: Clinical Operations Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 In Clinical Operations Oncology, we work with domestic and international co-development partners and overseas team
Basic purpose of the job HEOR Manager or Senior Staff will be responsible for and lead the development and implementation of the evidence generation strategy to maximize Boehringer Ingelheim asset value and optimize access to medicines
Basic purpose of the job The manager of RRL JP provides strong leadership to develop and implement regulatory strategy for the assigned products/projects as RRL JP, and exercises activities which include: An integral member of the
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through
General Information Job Advert Title: Global Translational Bioinformatics Lead Location: Nihonbashi,Tokyo Division: Early Development Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 Responsible for providing bioinformatics expertise to drug target selection, translational research, patient selection
General Information Job Advert Title: DWH Architect – Azure AWS Data Warehouse Location: Nihonbashi, Tokyo Division: DigitalX Employment Class: Permanent Description 【About Astellas】 As part of the Astellas commitment to delivering value for our patients, our
Our Team Our mission is to contribute improvement of quality of clinical development through GCP audit and to lead the inspection team to reduce the number of the observation raised during inspections. The GCP quality auditor: Independently
JOB DESCRIPTION Date: November 2024 Job Title: Medical Science Liaison Job Level: Associate Director Department: Medical Affairs Reports To: Sr. Director, Medical Affairs Location: Tokyo FLSA Status: N/A SUMMARY/POSITION OBJECTIVE: Briefly describe the general nature and
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.
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across
Job Description SummaryReviews, manages, proactively challenges, and controls status of projects operations of the programs and budgets; manages schedules and may prepares status reports. Assesses project issues and develops resolutions to meet productivity, quality, and stakeholders
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.
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。 Position Summary: The position is responsible for all the case processing and safety data management matters related to pharmacovigilance area activities for products both in development phase and in post-marketing phase. Primary roles & responsibilities include,
Career CategoryScientific Job Description Position Summary: The Manager will serve as a customer facing field medical lead to the medical/scientific community and will be responsible for establishing, developing and maintaining engagements and collaborations with prominent experts
Job Purpose The Director of TA Medical Affairs role is a senior leadership role, with the remit of building a world class Medical Affairs function, with the ultimate aim of providing overall leadership medical activities within
■ 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 order to verify
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
Head of Preclinical Development YOUR TASKS AND RESPONSIBILITIES: Oversee and support the following; Prepare the preclinical part of J-NDA and PAA dossiers (efficacy pharmacology, safety pharmacology, DMPK and toxicology) for successful registration of Bayer products in
