This position is responsible for supporting the management of operational processes in pharmacovigilance to ensure compliance with Sandoz global/local procedures and national/international regulations. · ...

We are a global team of over 3,500+ experts, bright thinkers, dreamers and doers changing the way the world experiences CROs in the best possible way. · We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-o ...

To support management of operational processes in ensuring compliance with Sandoz global/local procedures, · national and international regulations/standards/guidelines for pharmacovigilance of Sandoz marketed and investigational products. · ...

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. · We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, · bright thin ...

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an enviro ...

This position reports to Japan Safety PV Sr Mgr, Japan Safety PV Manager, or Japan Safety PV Manager and is responsible for performing safety activities under the guidance of senior managers. · ...

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.We look forward to welcoming your application. · ...

The Regional People Advisor will support the Regional Associate Director and Senior Director of People Operations with the implementation of the People Operations strategy and aligns with the company's objectives and organisation strategy. · ...

Regulatory project role with regulatory affairs responsibilities in a pharmaceutical company. Develop regulatory strategy for new drug developments and provide regulatory expertise within project/product teams. · Develop regulatory strategy for new drug developments, · Health Aut ...

PV associate in literature must participate in Global Literature Screening process, by providing review and assessment of the scientific and medical literature, according to procedures and regulatory requirements. · ...

+PV associate in literature must participate in Global Literature Screening process, by providing review and assessment of the scientific and medical literature, according to procedures and regulatory requirements. · ...

This role is responsible for ensuring optimal patient safety as first priority by developing a state-of-the-art safety strategy driving medical safety processes and capabilities having accountability for safety compliance in Japan. · Develop and maintain a local safety assurance ...

The PV Senior Specialist collaborates with colleagues to ensure compliance with local laws and regulations. They are responsible for all PV activities and may serve as the PV contact with local stakeholders. · Serves as the back-up PV Responsible person/QPPV as required per local ...

We are seeking a Business Development Associate who will help expand our global client network across the life sciences sector focusing on APAC region. · You'll collaborate with senior leaders to identify new business opportunities and connect with key decision-makers in pharma a ...

Leads the creation of the strategic global medical plan for Pharma Therapeutic Area product in alignment with countries' medical planning and global business function. · Liaises with key opinion leaders to support commercial success of Bayer Pharma products. · ...

A regulated pharmaceutical organisation is seeking a Pharmacovigilance (PV) Associate to support its drug safety and pharmacovigilance operations in Japan. · ...

Collaborate with Process Management Team members and Product Management Team members to ensure Safety communication and product stewardship · ...

The Associate Director of the Regulatory Affairs (RA) is responsible for managing regulatory affairs activities including pharmacovigilance work at RA department at PDRA division Animal Health in Japan. · Primary Activities · Support PDRA director to optimize/maximize PDRA's acti ...

Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditabl ...

We love investing in our staff by providing an excellent training and development platform. We value employee experience, · well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an envi ...

Based in our Office in Tokyo, Japan supporting Japan and other countries within the Asia Pac Region aligned to business growth, the Regional People Advisor: · ...