Pharma & Biotechnology Jobs in Palo Alto, Latest Pharma & Biotechnology Jobs in Palo Alto

The Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Provides expertise in translating regulatory requirements into practical, workable plans for project teams with international participants. May mentor and potentially supervise other regulatory professionals working on the project team and regulatory process-related topics. Requires ability to work strategically, both independe

This role is involved in the design, monitoring, and data analysis of the Company’s oncology clinical trials. As such, the Associate Director, Oncology Clinical Scientist is an important and visible member of the Oncology team. Key ResponsibilitiesProvide input to protocol design, provide oversight of clinical data (entry by sites, data completeness/accuracy working closely with ClinOps/Biometrics/Data Management teams), and support site and subject retention in clinical trials alongside the Med

PLEASE NO RECRUITERS!The VP of Clinical Operations, Oncology oversees three key functional areas (Clinical Operations, Data Management, and Clinical Trial Supply) to ensure efficient operation of clinical trials across Ascendis Pharma’s oncology pipeline. An ideal candidate has hands-on experience in executing global oncology trials from early to late phases. The candidate is expected to work cross-functionally to plan and execute global clinical trials, manage vendors, and ensure smooth collabo

Company DescriptionLVIS Corporation is on a mission to revolutionize the entire continuum of neurological care by developing AI driven software tools to help physicians accelerate patient throughput and improve patient diagnostic and treatment outcomes. We have an international team with our headquarters located in Palo Alto, California, USA, and we have an office in Gangnam, Seoul, South Korea. We are looking for talented individuals to join us in our mission to transform the neurology health c

Company DescriptionLVIS Corporation is on a mission to revolutionize the entire continuum of neurological care by developing AI driven software tools to help physicians accelerate patient throughput and improve patient diagnostic and treatment outcomes. We have an international team with our headquarters located in Palo Alto, California, USA, and we have an office in Gangnam, Seoul, South Korea. We are looking for talented individuals to join us in our mission to transform the neurology health c

We’re Exai Bio.Our mission is to deliver the earliest and most accurate diagnosis of cancer. We aspire to enable a world where cancer can be detected early, diagnosed accurately, treated in a personalized and targeted way, and ultimately cured. And we’re looking for a Quality Engineer. We’re hiring an experienced quality professional to join our growing team. You will play an integral part in developing a Quality System compliant with ISO 13485 and FDA QSR regulations. You will lead the implemen

We’re Exai Bio.Our mission is to deliver the earliest and most accurate diagnosis of cancer. We aspire to enable a world where cancer can be detected early, diagnosed accurately, treated in a personalized and targeted way, and ultimately cured.And we're looking for and Associate Scientist. Exai Bio is seeking a highly motivated associate scientist to contribute to our research and early development program in support of our next-generation liquid biopsy platform. In this role, the associate sci

Company DescriptionLVIS Corporation is on a mission to revolutionize the entire continuum of neurological care by enabling AI driven digital analytics to help physicians accelerate patient throughput by transforming signal analysis and visualization. The LVIS software, NeuroMatch, utilizes brainwave signals from traditional EEG systems to enable AI driven algorithms to perform EEG source localization, spike and seizure event detection. We have an international team with our headquarters located

Hi, we’re Exai Bio.Our mission is to deliver the earliest and most accurate diagnosis of cancer. We aspire to enable a world where cancer can be detected early, diagnosed accurately, treated in a personalized and targeted way, and ultimately cured. And we’re looking for a Facilities Coordinator. We’re looking for a proactive facilities coordinator to join our growing team and help with various facilities-related responsibilities in our Palo Alto lab and office. Your daily tasks may include gener

ResponsibilitiesThe Senior Clinical Data Manager will be responsible for leading and coordinating Data Management(DM) deliverables from database design amp; set-up, through cleaning and reporting to databaselocking, ensuring that the completeness, accuracy, and consistency of clinical data meets the qualitystandards and regulatory requirements for analysis and reporting.This includes:- The EDC build (set-up, eCRF design, database validation, etc) and user acceptance testing (UAT), study data cl

What We are Looking ForA highly motivated senior research associate to join the Reagents Development team. As a member of the Reagent Development team, the successful candidate will contribute to the development of robust reagents and QC methods, and support the transfer of our next-generation liquid biopsy platform from design to production in a CLIA lab facility. In this role, the candidate will work closely with the assay development and automation teams to develop effective reagents that per

What We are Looking ForThe Director of Clinical Operations will be responsible for providing leadership to the ClinOps team and for ensuring studies within a program are being managed in accordance with the company’s overall program goals, timeline, budget and quality expectations.Tasks may include development and implementation of clinical monitoring standards and best practices for effective clinical monitoring of investigational sites in accordance with regulations for identifying and leading

Job SummaryThe Senior Quality Engineer is responsible for taking the lead in establishing, implementing andmaintaining systems and/or services to measure and improve product quality, cost, and customer service while ensuring full compliance to US FDA, ISO 13485, and applicable International Quality Management System requirements. The Senior Quality Engineer will be responsible for driving activity around process validation, as well as participating in establishing and monitoring systems related

What You’ll Do- Assist in leading project management (PM) activities for a series of high-performing, cross-functional projects across research and product development with diverse teams - Apply Project Management best practices in the development, initiation, planning, execution, control, prioritization and closing of projects - Manage and track budgets and resources to assure efforts follow project/study guidelines - Assist in facilitating and managing team meetings and relationships, set

At LVIS, our objective is to innovate how neurological diseases are diagnosed and treated by creating advanced brain networkanalysis tools. LVIS is a lean team of science researchers, clinical researchers, engineers, and designers from a variety of impressive backgrounds.As the Office manager / HR manager you'll contribute to a fast growing organization by assisting with the efficient running of the main office of LVIS and by managing the HR and recruitment functions. Your time will be approxima

About usAt LVIS, our objective is to innovate how neurological diseases are diagnosed and treated by creating advanced brain networkanalysis tools. LVIS is a lean team of science researchers, clinical researchers, engineers, and designers from a variety of impressive backgrounds.As a Senior UX Designer, you will apply principles of design thinking to create intuitive interfaces that directly solve the needs of physicians and other healthcare professionals. We are looking for a motivated designer

The Associate Director (AD) is responsible for effective conduct of Ascendis’ global and regional clinical trials. As a key member of the cross-functional team driving Ascendis’ clinical trials to completion according to agreed timelines and quality, the AD / Sr. CTM contributes directly to Ascendis’ focus on making a meaningful difference in patients’ lives and is part of a global organization with locations in US, Germany, and Denmark.The role is based in Palo Alto, CA or may be remote and rep

Head of Global Medical Safety Science reports to VP, Head of Pharmacovigilance and Global Drug Safety. Located within Global Safety department, the Head of Global Medical Safety Sciences is a leadership role and has global responsibility for safety sciences support of all development and marketed products in Ascendis portfolio to meet GVP requirements. This role will lead the global medical safety science team in the analysis of safety data, identifying, detecting and investigating safety signal

The successful candidate will be the clinical lead of the first randomized study for TransCon TLR7/8 Agonist and/or TransCon IL-2bg, providing critical input for protocol development along with medical monitoring, regulatory interactions, safety assessments, and engagement with key opinion leaders and investigators. The position will be based in Palo Alto.Key Responsibilities- Develops and executes protocols in the TransCon TLR7/8 Agonist and/or TransCon IL-2bg program - Engages effectively wit

The Manager, Global PV Operations reports directly to the Head of Global PV Operations. Under the direction of the Head of Global PV Operations, is responsible for all assigned Ascendis Drug Safety PV Operations related activities for all products in the Ascendis portfolio. This individual has accountability for the assigned PV Operations activities in Ascendis.Key Responsibilities- Support Study Management Teams (SMTs) as an active member representing PV Operations team.- Participate in the con