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The Area Study Start-Up Lead is a key role responsible for ensuring the successful initiation, execution, and maintenance of clinical studies within a specified region. Reporting to the Associate Director, Area Study Start-Up, this position serves as the central point of accountability for the timely, cost-effective, and high-quality delivery of site start-up and maintenance activities.
The Clinical Research Lead is a critical driver of product development initiatives, providing leadership and oversight to ensure the successful execution of clinical trials. This role plays a vital part in facilitating the advancement of our life-changing medicines through effective management and engagement with various stakeholders.
As the Post-Approval Studies Manager, you'll lead our client's efforts in overseeing and driving the success of post-approval studies, ensuring compliance, high-quality data, and effective stakeholder collaboration. The role will have the opportunity to understand what's it like to post market for meds.
As a Medical Advisor with Our Client, you will have the privilege of working at the forefront of medical innovation. Collaborating with a team of experts, you will contribute to bringing life-changing therapies to patients in Taiwan. Your expertise and unwavering commitment will be instrumental in advancing the company's mission to enhance healthcare outcomes and improve lives.
As the Medical Director, you will serve as the foremost medical representative in the country. You will be responsible for implementing both short- and long-term medical strategies derived from the global, regional, and IM (Innovative Medicines) teams, while forging impactful strategic alliances with healthcare communities and government bodies.
Concentrating on scientific communication regarding Cardio-Renal-Metabolism, encompassing product information and new applications. Delivering scientific data to SEs/HCPs, executing medical programs, and supporting their requirements within the designated area.
My client is seeking a highly skilled and self-motivated Biotechnology Clinical Research Scientist to join our dedicated team. As a Biotechnology Clinical Research Scientist, you will be responsible for independently planning and preparing a wide range of clinical documents for clinical drug development. Your expertise will be instrumental in organizing, analyzing, and interpreting scientific and statistical data to advance our biotechnological solutions.
The position entails providing leadership and guidance to field service and repair center teams. You will play a key role in driving the achievement of business goals, overseeing commercial and operational activities. Collaboration with various departments such as Sales, Marketing, CS, Distribution, and RAQA will be crucial in this role.
The role will support hemophilia, new product launches, and support global clinical development programs in Taiwan, and is responsible for acting as an expert in the creation of the medical strategy and operationalization of the medical activities as a key member of the Brand Team. And build up external partnerships with KOLs.
Allocate new product and provide marketing strategy and campaigns for sales team and department
Your expertise in comprehensive project management, from risk assessment to clinical trial execution, will be instrumental in driving the success of impactful initiatives. This role not only offers a lucrative career opportunity with a competitive annual salary but also provides a dynamic environment for seasoned professionals to leverage their experience and advanced education, influencing the trajectory of biotechnological advancements.
The (Sr) MSL is the leader in designated therapeutic areas to provide scientific support to internal stakeholders and external thought leaders, to establish a professional presence for the company.
Take lead in its territory responsible to sales revenue, expend market reach while maintain relationship with clients.
Taking charge of various markets in Asia and drive business revenue
For Regulatory Affairs (Mainly for medical devices) & Quality Assurance & People Management
Our client is currently seeking a highly motivated and skilled professional to join their team as a Communication and Reimbursement Specialist. In this role, you will play a crucial part in shaping communication strategies and driving market access initiatives. Your responsibilities will encompass a diverse range of tasks aimed at effectively engaging with various stakeholders, including policymakers, stakeholders, and patient advocacy groups (PAGs).
responsible for building up the Taiwan RA foundation
The Regulatory Affairs Department obtains and maintains marketing approvals of responsible products in Taiwan. It ensures full local regulatory and company compliance and provides regulatory expertise to support clinical research, product launches, and business development so as to assist in achieving business growth and full compliance with legal requirements for pharmacovigilance regarding regulatory affairs' relevant responsibilities.
帶領團隊發展業務，透過自身經驗規劃業務分區並達到業績目標
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