Healthcare professionals, HAs, ECs, DMCs, and Academia. Line management responsibility of Director/Associate Director Global...) to receive an alert: × Select how often (in days) to receive an alert: Senior Director -Safety Surveillance Facility: Reg...
formal oncology training) of experience at a pharmaceutical or biotechnology company as a (Associate) Medical Director...Job Title: Senior Medical Director, Clinical Development - Oncology Job Location: Brisbane, CA, USA Job Location...
formal oncology training) of experience at a pharmaceutical or biotechnology company as a (Associate) Medical Director...Job Title: Senior Medical Director, Clinical Development - Oncology Job Location: Hayward, CA, USA Job Location...
and inspires. POSITION OVERVIEW: Reporting to the Senior Director, Research Quality Assurance, the Associate Director/ Director... Practices (GLP), and Good Pharmacovigilance Practices (GVP) quality systems within Disc Medicine. This hands-on director-level...
Associate Director, Global Patient Safety and Risk Management—Global Safety Systems will be responsible for configuring.... A comprehensive and rigorous approach to pharmacovigilance activities allows us to have a compliant global pharmacovigilance system...
formal oncology training) of experience at a pharmaceutical or biotechnology company as a (Associate) Medical Director...Job Title: Senior Medical Director, Clinical Development - Oncology Job Location: Hayward, CA, USA Job Location...
at a pharmaceutical or biotechnology company as a (Associate) Medical Director. Must have experience in oncology or malignant hematology...The Senior Medical Director, Clinical Development will be an essential contributor to the scientific, clinical...
on , , , and . Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product Safety... regulations related to pharmacovigilance supporting all patient safety activities. Experts on hematology-oncology late stage group...
submissions and responses, and other program documents. May oversee the work of Associate Medical and/or Scientific Directors... discussions. Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures...
: Reg Affairs & Safety Pharmacovigilance Location: Clayton, NC, US About the Department You will be joining Fill... Nordisk and help us make what matters. The Position Manage a team of Associate Managers, documentation area specialists...
Associate Director, Quality Assurance. The Sr. Clinical QA Manager will support global clinical studies for one or more product..., Pharmacovigilance, Legal and Regulatory Affairs) regarding clinical quality matters, providing regular updates on audit outcomes, CAPA...
of Clinical Development systems and processes. The Sr. Clinical QA Manager will report to the Associate Director, Quality..., Pharmacovigilance, Legal and Regulatory Affairs) regarding clinical quality matters, providing regular updates on audit outcomes, CAPA...
as a regulatory liaison to clients and internal functional departments. Relationships Reports to: Associate Director, Regulatory...: Reg Affairs & Safety Pharmacovigilance Location: Bloomington, IN, US About the Department At Novo Nordisk, we want...
to share best practices. This role reports into the Global Medical Information Director. Responsibilities include... stakeholders (e.g., Quality, Pharmacovigilance, RandD etc.) to develop and maintain a library of approved medical information...
Project Manager Department: Clinical Development Operations, R&D Line Manager: (Senior) Director /Clinical Program... Director (CPD) Location of the role: UK (London) or France (Les Ulis) or USA (Cambridge) Purpose of the position Sr...