and without compromise. Define and lead initiatives of all Clinical Trial Supply Management IMPM-Portfolio activities in global..., if applicable. At least 5 years of experience in Clinical Trial Supply Management within the pharmaceutical or biotech industry...
one or more complex/large scale clinical trial/s in either early or late stage clinical development within a program Lead communications...(s) Ensure inspection readiness throughout the clinical program lifecycle May be responsible for line management...
Responsibilities Clinical Research Operations. Directs team leaders overseeing clinical research management...: clinical research coordinators, regulatory operations, and research data management. Policies and Procedures. Sets...
to be involved in all aspects of clinical trial execution. Responsibilities: Assist with audit of central files Assist with the... Director, Clinical Operations with tracking of financial documents. Assist with creation of presentations of clinical research...
Associate Director, Clinical & Quality Process Compliance is responsible for ensuring the quality of processes and product.... Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... and mitigations are in place. Leads the clinical pre-approval inspection (PAI) readiness programs, the management of the inspection...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... and mitigations are in place. Leads the clinical pre-approval inspection (PAI) readiness programs, the management of the inspection...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid.... Leads the clinical pre-approval inspection (PAI) readiness programs, the management of the inspection and the response...
Job Description: Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA Duration: 12... are in place. Leads the clinical pre-approval inspection (PAI) readiness programs, the management of the inspection and the...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid.... Leads the clinical pre-approval inspection (PAI) readiness programs, the management of the inspection and the response...
Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 9893 Responsibilities The Associate Director... assigned Collaborates with key internal stakeholders to ensure that 1) clinical trial risks are detected and remediated...
: As Associate Director, Clinical Science, you will work in a cross-functional clinical matrix team, fostering a collaborative... for various clinical trial activities including optimizing clinical trial processes, proactively identifying risks, implementing...
Associate Director, Clinical Imaging in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry.... Here, you will be a vital contributor to our inspiring, bold mission. POSITION OBJECTIVES: The Research Associate Director (RASD) Clinical...
Associate Medical Director leads and drives strategy for the overall global (US/EU/Japan/China) clinical development taking... Director, Clinical Science, Neuroscience- Pulmonologist/Neurologist in our Cambridge, MA office. At Takeda...
About This Role: As an Associate Medical Director, Clinical Development – Immunology, you will be an integral member... to the Executive Director, you will be instrumental in crafting the clinical development strategy and leading the execution...
better, longer. For more information, visit us at . About the Role Associate Director, Clinical Science As the Associate... Director, Clinical Science reporting to the Director, Clinical Science, you will play a key role in one of our ongoing clinical...
clinical trial team meetings, tracking key study metrics (e.g., enrollment, site feasibility, and data collection) to ensure... medicines to those who need them, improve the understanding and management of disease, and give back to our communities through...
Director of Clinical Data Management, the Senior Manager of Clinical Data Management will be responsible for managing clinical... data management activities across Tango's clinical trials. This includes overseeing study-specific data management...
Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality of processes and product.... Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects...
Job Title: Associate Director, Global Scientific Communications Lead Location: Cambridge, MA 02142:: Remote Duration...: 12 Months 8 AM to 4 PM Objectives/Purpose The Associate Director, Global Scientific Communications Lead is a key...