Regulatory Submission Coordinator Jobs in South San Francisco

Clinical Research Coordinator Duties: Assist with the management ... a daily basis the Study Coordinator will assist faculty with these ... including the OnCore database. The coordinator will organize and..

... will serve as Lead Study Coordinator for the Delish Study at ... overlapping waves. The Lead Study Coordinator will recruit and enroll participants ... through 12-month follow-up assessments. u003cbr/u003eu003cbr/u003eThe..

:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Institutional Review Board (IRB) Administrator supports the UCSF Office of Ethics and Compliance and the UCSF mission to advance health worldwide. S/he does this by working closely with ..

Title: Process Lead Coordinator Location: San Francisco, CA Duration: 6 months US Medical Affairs Responsibilities will include several aspects of operational systems and tools, methodology and processes, reporting and other communications ..

... for the position of Clinical Regulatory Affairs Manager. Primary responsibilities include ... Primary responsibilities include implementing global regulatory strategies with managerial oversight, independently ... support preparation and maintenance of..

Regulatory Intelligence Project Manager Responsibilities: Identify, ... Develop new or update existing regulatory policies, processes and SOPs and ... to determine the impact of regulatory changes on the business. Manage..

:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Research Services Coordinator, Contracts and Grants (RSC) is UCSF’s Office of Sponsored Research (OSR) institutional representative for faculty and is the primary point of contact for external sponsors ..

n DIRECTOR, SUPPLY CHAIN                                                        Day One Biopharmaceuticals is an emerging, mission-driven, drug development company intentionally designed to identify, clinical evaluate, and successfully commercialize novel treatments for pediatric oncology patients, and ultimately ..

... Interprofessional Practice and Education (PIPE) Coordinator applies knowledge about curriculum, requirements ... compliance, and program accreditation.u003cbr/u003eu003cbr/u003eThe PIPE Coordinator works closely with the PIPE ... interprofessional curriculum development and implementation.u003cbr/u003eu003cbr/u003eThe..

nSENIOR CLINICAL TRIAL  SPECILAIST                                         Day One Biopharmaceuticals is an emerging, mission-driven, drug development company intentionally designed to identify, clinical evaluate, and successfully commercialize novel treatments for pediatric oncology patients, and ultimately ..

BioMarinu2019s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that ..

nCLINICAL TRIAL SENIOR SPECILAIST                                         Day One Biopharmaceuticals is an emerging, mission-driven, drug development company intentionally designed to identify, clinical evaluate, and successfully commercialize novel treatments for pediatric oncology patients, and ultimately ..

... review plans, and responses to regulatory agency questions regarding scientific aspects ... and presentation, and ensuring that regulatory agency questions (where relevant) have ... Affairs input in preparation of..

:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEW u003cbr/u003eThis Research Center Program Manager position manages the research operations and day-to-day activities of the Hyperpolarized MRI Technology Resource Center (HMTRC) and related research projects led by Center ..

u003cpu003eFounded in 1965, Telecare is a rapidly growing mental health care company dedicated to making a difference for our clients, the community, and our employees. We offer an array of mental ..

nMyovant Sciences aspires to be the leading healthcare company focused on innovative treatments for women’s health and prostate cancer designed to improve the lives of millions.  We are on a mission ..

The Director, Regulatory Writing plans, authors and manages ... Writing plans, authors and manages regulatory/clinical documents to support clinical development ... support clinical development programs and regulatory submissions. Assists with..

Sutro is looking for a Director level candidate to join our Clinical team. The Clinical Scientist is a key cross-functional team member contributing to the design and execution of Sutro’s clinical ..

Job Information Stryker Senior Regulatory Affairs Specialist (Remote) in Fremont ... organization by visiting stryker.com Why regulatory affairs/quality assurance at Stryker? Are ... do! Here, we provide our Regulatory Affairs..

Are you ready to use your experience and expertise to make an impact on patients' lives? Astellas Gene Therapies is a biotechnology company developing new genetic medicines for rare, life-threatening diseases. ..

... review plans, and responses to regulatory agency questions regarding scientific aspects ... and presentation, and ensuring that regulatory agency questions (where relevant) have ... Affairs input in preparation of..

:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe overall purpose of the position is to serve as Lead Statistical Analyst and Project Coordinator for a portfolio of research projects in cardiovascular and metabolic disease in support ..

... the Investigational Trials Resource (ITR) regulatory protocol editor for investigator initiated ... and Institutional Review Board (IRB) submission, contract execution, and billing set ... in a related position including..