Merck

This role is a Medical Science Liaison (MSL) for Oncology at Merck in Tokyo, Japan. The primary responsibilities involve engaging with Key Opinion Leaders (KOLs) and Stakeholders to provide scientific information, gather insights on unmet medical needs and data gaps, and share the latest scientific information internally. The role requires adherence to internal and external regulations related to pharmaceutical sales and information provision.

Merck is seeking a Business Development and Alliance Management Associate Director in Tokyo, Japan, to develop and implement business development strategies, identify partnership opportunities, and manage alliances to maximize the company's product portfolio within the healthcare industry. The role requires strong strategic planning, negotiation, and communication skills, with a focus on the biotech/pharmaceutical sector.

This role is a General Affairs Specialist Office Support position at Merck, focused on supporting employees with disabilities through job coaching and employment support services. The primary responsibilities include business support tasks, cafe operations, social skill development, collaboration with external parties, and planning/execution of disability hiring initiatives. It requires strong communication, problem-solving, and ethical conduct.

This role at Merck focuses on medical affairs within oncology, involving the design, planning, and execution of medical research, development of country medical affairs plans, and engagement with scientific leaders. It requires clinical and research experience in healthcare, knowledge of pharmaceutical regulations, and experience with scientific publications or presentations. The role emphasizes strategic thinking, scientific communication, and fostering collaboration within a global context.

This role is a Senior Specialist in R&D Clinical Quality Assurance at Merck, focusing on ensuring data integrity and compliance with global regulatory requirements in clinical trials across the APAC region. The primary responsibilities include conducting GCP audits, preparing audit reports, collaborating with various teams to resolve observations, and supporting the overall quality assurance processes within clinical development.

This role at Merck focuses on clinical research in oncology, involving the planning, execution, and reporting of clinical trials. The scientist will collaborate with internal and external stakeholders, including regulatory bodies, to support the global development of new oncology drugs. Responsibilities include inputting into development strategy, preparing regulatory submission documents, managing clinical trial protocols, monitoring data, and contributing to publications.

This role is for a Clinical Research Manager at Merck, focusing on leading clinical trial operations in Japan. Responsibilities include managing trial planning, execution, and closure, leading a team, managing costs and risks, and ensuring quality and compliance. The role requires strong English and Japanese language skills, and experience in clinical research management or as a Project Leader at a CRO.

This role is for an Associate Clinical Research Manager (aCRM) in the General and Specialty Medicine/Infectious Diseases & Vaccines CRM domain at Merck, with a career path towards becoming a Clinical Research Manager (CRM). The aCRM will gain skills and knowledge in clinical trial operations under the guidance of a CRM, potentially also performing CRA duties. The CRM role involves leading clinical trial operations in Japan, collaborating with US counterparts, managing trial teams, vendors, costs, milestones, risks, and supporting site-level issue resolution.

This role focuses on building and executing regulatory affairs strategies for new drug development in Japan, aligning with global strategies. It involves significant interaction with regulatory authorities like MHLW and PMDA, ensuring the quality of submission documents, and coordinating the preparation and submission of applications. The position requires a background in life sciences, experience in pharmaceutical development and regulatory submissions, and strong English communication skills for international coordination.

This role at Merck focuses on medical review of materials and slides, internal compliance training, and leading cross-functional projects within the Medical Affairs domain. It requires experience in pharmaceutical medical affairs or related departments, a life sciences background, and business-level English proficiency. The core responsibilities involve ensuring compliance and managing medical communications.

Associate Director of Regulatory Affairs responsible for managing regulatory affairs and pharmacovigilance activities for animal health products in Japan. This role involves ensuring timely product registrations, optimizing development plans, and leading a team to comply with pharmaceutical guidelines and local laws.

Director, Policy/Government Relations Health Policy at Merck in Tokyo, Japan. This role involves developing and executing strategies for vaccine policy, engaging with stakeholders, and leading cross-functional teams to advance vaccine business and public health initiatives. Requires extensive healthcare experience, deep knowledge of Japanese healthcare policy, and strong communication skills.

Merck is seeking a Medical Science Liaison (MSL) for their General & Specialty Medicine business unit, focusing on the Cardiometabolism therapeutic area in Tokyo, Japan. The role involves engaging with medical and scientific leaders to gain insights, sharing these insights with stakeholders, and driving healthcare improvements. It requires strong scientific knowledge, communication skills, and strategic thinking. The position is open to experienced MSLs or individuals from academia with a Master's degree in life sciences and business-level English proficiency.

This role focuses on medical affairs and scientific content creation within the oncology domain at Merck. The specialist will contribute to medical strategy by responding to medical information requests, analyzing stakeholder insights, creating academic materials, reviewing promotional materials, and providing scientific consultation. The role requires at least 3 years of experience in a healthcare-related field, with a preference for experience in Medical Affairs or Medical Writing, and a relevant scientific degree or license.

Merck is seeking a Medical Affairs General & Specialty Medicine MSL Manager to lead a team of MSLs, improve team performance, and contribute to scientific discussions and problem-solving. The role involves managing MSL activities, ensuring compliance with regulations, developing educational plans, and supporting the hiring and retention of team members. The ideal candidate will have a strong understanding of strategy, communication, problem-solving, and negotiation skills, with a Master's degree in Pharmacy, Pharmacology, or Life Sciences, and at least 3 years of experience in Medical Affairs and as an MSL.

Associate Director in Quality Control for Merck's Manufacturing Division, responsible for leading a team of quality control laboratory analysts and managing quality testing for raw materials, components, and finished drug products in a pharmaceutical manufacturing setting. Ensures compliance with cGMP, safety, and environmental regulations, manages quality systems, investigations, and corrective actions. Oversees method transfers, safety measures, budget forecasting, and continuous improvement initiatives. Requires a Bachelor's degree in a science/life science field, at least 8 years of experience in pharmaceutical quality operations/control with 3 years of people management, and strong understanding of analytical methodology and regulatory standards.

Merck is seeking a Medical Advisor for Cardiometabolism in Tokyo. The role involves creating and executing domestic medical plans (CMAP), engaging with stakeholders, generating evidence, and contributing to medical education. Requires advanced scientific/medical knowledge, collaboration skills, strategic thinking, and leadership. The position focuses on delivering innovative medicines to patients and healthcare professionals.

This role focuses on developing and executing Health Economics and Outcomes Research (HEOR) strategies for pharmaceutical assets, generating evidence to support market access, pricing, and reimbursement in Japan. Responsibilities include conducting economic analyses, developing value dossiers, managing literature reviews, performing database analyses, and coordinating cross-functional efforts.