Associate Director, Clinical & Quality Process Compliance is responsible for ensuring the quality of processes and product... of projects impacting clinical and safety quality. Actively identifies key areas for process improvements and develop...
Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality of processes and product... of projects impacting clinical and safety quality. Actively identifies key areas for process improvements and develop...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... as a Strategic Quality Thought Partner to Clinical Program Teams and other key stakeholders in the delivery of the clinical research...
Job Description: Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA Duration: 12...+ Months (Possible of Extension) Job Overview Provides quality assurance oversight of the global clinical research programs...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid... role - Shift: 8 AM to 5 PM OBJECTIVES: Provides quality assurance oversight of the global clinical research programs...
Clinical QA Compliance supports and oversees the proactive and risk-based Quality Strategy implementation in the clinical... oversight on the clinical trial process to ensure continuous inspection readiness and compliance with Regulatory Authorities...
Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 9879 The Associate Director Clinical Data... clinical portfolio/platform program(s). The ADCDM is working closely with the (Senior) Director Clinical Data Management...
, Biometrics, the Associate Director of Clinical Data Management will be responsible for leading the clinical data management.... This position will initiate best practices and lead clinical data management process flow as well as support the oversight of data...
Job Description General Summary: The Associate Director, GMP Operational Quality will provide leadership... and quality oversight for contract testing laboratories (CTLs) supporting Vertex’s biologics and combination product portfolio...
compliance with global standards, and for ensuring accuracy and scientific rigor of publications. The Associate Director...Job Title: Associate Director, Scientific Communications Lead (Hematology, Global Medical Affairs Oncology) Location...
with prime sites for Alexion to facilitate discussion and consultation around site compliance to ICH GCP and process improvements... in the office while respecting individual flexibility. Join us in our unique and ambitious world. The Role: As Associate...
with prime sites for Alexion to facilitate discussion and consultation around site compliance to ICH GCP and process improvements... in the office while respecting individual flexibility. Join us in our unique and ambitious world. The Role: As Associate...
The role of Associate Medical Director – Primary Care Informatics offers a unique opportunity for a practicing primary.... Position Summary The Associate Medical Director – Primary Care Informatics is a practicing primary care physician...
that all information I submit in my employment application is true to the best of my knowledge. Job Description Associate Director...: Join Takeda as the Associate Director, Lifecyle Management, GIBU, where you will lead efforts to maximize brand's value by owning...
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...
that all information I submit in my employment application is true to the best of my knowledge. Job Description Associate Director..., In Vivo Digital Portfolio & Data Stewardship About the Role We are seeking an experienced Associate Director of In Vivo...
Associate Director will participate in the shaping and execution of HEOR strategies that optimize the value proposition.... This position reports to the Senior Director HEOR, CF and Early Pipeline. Key Duties and Responsibilities: Leads execution...
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence...-quality medical affairs education and training plans and materials to drive a consistent and deep understanding of, scientific...
by developing medicines that provide truly meaningful improvements in quality of life and survival for people with cancer... to advance clinical stage programs and further develop commercial stage assets. We are looking for an experienced hands...
(CROs) to maintain quality, consistency, and compliance with CDISC standards and regulatory requirements. Provide hands.... Oversee CRO partnership, including scope negotiation, timeline oversight, and quality monitoring and audits. Anticipate...