ich jobs in Vancouver

Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team....

TRIO - Translational Research in Oncology in Canada is seeking a Clinical Research Associate to join the Monitoring Resources team. This remote position supports Western Canada (BC/AB/SK/MB) and reports to the CRA Line Manager. The role involves site visits, regulatory compliance, data verification, and collaboration across teams.You will work independently...

Translational Research in Oncology (TRIO)is a global academic clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource...

Xenon Pharmaceuticals is on the lookout for a Senior Manager/Associate Director of Quality Control. This role emphasizes leadership in quality compliance for drug substances and products within an inclusive work culture. Located in Vancouver or Boston, you will manage analytical testing, stability programs, and adherence to ICH and cGMP regulations. This...

Manage Canadian clinical trial start-up submissions using Health Canada knowledge and precise regulatory documentation from a remote position. Coordinate approvals and timelines for Premier Research projects.As a Site Start-up Associate II, you support Premier Research’s Clinical Monitoring, Site Management and SSU team. You prepare Central and Local EC or...

Surveillez des essais cliniques en oncologie pour IQVIA depuis votre domicile dans l’est du Canada, en français et en anglais.Comme attaché de recherche clinique II expérimenté, vous assurez la conformité des essais de phase I à IV aux protocoles, aux BPC/ICH et aux exigences réglementaires. Vous gérez les activités des sites du démarrage à la...

TRIO - Translational Research in Oncology is seeking a Clinical Research Associate to join our Monitoring Resource team. This remote, full-time freelance opportunity is a 1-year contract open to candidates in Western Canada (BC, AB, SK, MB).Responsibilities include site visits, data verification, and ensuring FDA/ICH-GCP compliance while mentoring junior...

Attaché de recherche clinique II IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. Aperçu du poste L'ARC II est responsable de la surveillance des essais cliniques de phase I à IV afin d'assurer la...

## Senior Clinical Research Associate (Canada)Apply: Remote: Canada: Part time: Posted 18 Days Ago: R6995Premier Research is looking for a Senior Clinical Research Associate (Canada) to join our Functional Services Provider (FSP) team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough...

## Drug Safety AssociateApply: Remote, ON: Full time: Posted Today: R2617957Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come...

## Drug Safety AssociateApply: Remote, ON: Full time: Posted Today: R2617957Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come...

## Site Start up Associate II (Canada Regulatory Affairs)Apply: Remote: Canada: Full time: Posted 11 Days Ago: R6981Premier Research is looking for a Site Start up Associate II (Canada Regulatory Affairs) to join our Clinical Monitoring, Site Management and SSU team.You will help biotech, medtech, and specialty pharma companies transform...

Principal Medical WriterThe Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with...

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.QA OFFICERFull Time Vancouver, BC, Vancouver, BC, CA5 days ago Requisition ID: 1882Salary Range: $50,000.00 To $55,000.00 AnnuallyQuality Assurance OfficerJob Title : QA Officer IFrontage is a global...

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. About MMS MMS is an innovative,...

Job Description Job DescriptionTranslational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is seeking a Clinical Research Associate...

Manager, Quality AssuranceLocation: West Coast US+Canada (Hyrbid)The Manager, Quality Assurance, is responsible for ensuring investigational medicinal products (IMPs) meet current Good Manufacturing Practices (cGMP). This role serves as a quality partner to internal teams, executing hands-on batch reviews, investigations, vendor management and compliance...

Worldwide Clinical Trials is seeking a Project Manager to oversee clinical trials from start-up to close-out. You will lead cross-functional teams, manage resources with functional heads, and ensure deliverables meet time/quality/cost expectations across local, regional, or global scopes. The role requires 5+ years in clinical pharmaceutical project...

Company Chronic kidney diseases are a severe and growing worldwide health challenge that affects 1 in 7 people. Without effective treatments patients can experience kidney failure leading to dialysis and transplantation, a high burden to patients, families and the health care system. Despite recent advances for certain kidney disease patients, many forms of...

## Drug Safety AssociatePostuler: Remote, ON: Temps Plein: Publié aujourd'hui: R2617957**À propos de Cencora**Cherchez-vous à faire une différence dans la vie d’un patient? Chez AmerisourceBergen, vous trouverez une culture innovante et collaborative, axée sur le patient et soucieuse de faire la différence. En tant qu’organisation nous...