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If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational 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...

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational 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...

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas including immunology, oncology and neuroscience - and products...

Working under general direction of the Manager and/or Director, the Clinical Trial Associate is assigned on Alzheimer’s clinical research trials regulatory tasks. Clinical Trial Associates are primarily responsible for compliance with current regulations, policies, procedures, coordination regulatory documentation activities, IRB submissions, maintain...

Senior Scientist, Research and Product Development (Mandarin Speaking Analytical SME) Join to apply for the Senior Scientist, Research and Product Development (Mandarin Speaking Analytical SME) role at SteriMax Inc. The Research and Product Development (RPD) group at SteriMax Inc. is primarily responsible for dossier review, co‑development, in‑licensing...

- Directing the staff and activities of Analytical Research & Development - Develop testing methods for drug substance and drug product - Provide recommendations to management on enhancing productivities by using advanced lab automation equipment - Reviews and approves regulatory submission and other technical reports generated by the Analytical...

- Lead the staff and operations within Analytical Development responsible for all mass‑spectrometry‑based studies - Oversee all LC‑MS and GC‑MS projects ensuring scientific excellence and regulatory compliance - Provide technical leadership to scientists and senior chemists - Guide team in conducting complex investigations - Consult with other...

- You will design, maintain, and drive the adoption of SCM standards—component definitions, metadata schemas, taxonomy, lifecycle governance, and content quality frameworks—across R&D. - Ensures all SCM artefacts are audit-ready, compliant with regulatory requirements, and fit for automated downstream consumption, including AI-assisted and generative...

The ESO SRT Quality Lead ensures that all sterile Galderma products produced by Contract Manufacturing Organizations (CMOs) meet the highest quality standards and comply with relevant government regulations. This includes adherence to cGMP, GDP, ISO, ICH, and other applicable regulations and guidance. The role leverages regulatory, industry, and technical...

ESO SRT Quality Lead Avec un héritage unique en dermatologie ainsi que des décennies d'innovation de pointe, Galderma est le leader émergent de sa catégorie dédié entièrement à la dermatologie, présent dans environ 90 pays. Nous proposons un portefeuille innovant, basé sur la science, de marques phares haut de gamme et de services qui couvrent...

Role: Pharmacovigilance Specialist (Remote) Location: Remote (Work from Anywhere) Job Type: Contract Payout: $70 - $80/hour Role Overview: We are hiring for one of our clients, seeking a Pharmacovigilance Expert to work on a contract basis. This role involves monitoring, evaluating, and reporting adverse events related to pharmaceutical products to ensure...

Avec un héritage unique en dermatologie ainsi que des décennies d'innovation de pointe, Galderma est le leader émergent de sa catégorie dédié entièrement à la dermatologie, présent dans environ 90 pays. Nous proposons un portefeuille innovant, basé sur la science, de marques phares haut de gamme et de services qui couvrent l'ensemble du spectre du...

Role: Medical Writer (Remote) Location: Remote (Work from Anywhere) Job Type: Contract Pay out: $50 - $80/hour Role Overview: We are hiring for one of our clients in the healthcare industry, seeking a Medical Writer / Clinical Document Author to develop regulatory documents for clinical studies. The role involves preparing clinical study reports, protocols,...

Indero in Montreal, Canada, seeks a Project Manager to oversee clinical research projects from initiation to closure. You will ensure budgets, scope and timelines are met while complying with SOPs, GCP/ICH standards and regulatory requirements, under supervision by senior management. The role emphasizes disciplined project management, cross‑functional...

Parexel FSP in Canada seeks a Clinical Research Manager to lead end-to-end study delivery in ICH/GCP environments, coordinating between Country Operations, the clinical trial team, and external partners. You will drive feasibility, site selection, recruitment, execution and closeout, mentoring local teams, ensuring CTMS/eTMF compliance, and balancing budgets...

Alberta Health Services is seeking an RN with oncology and clinical trials experience to support coordination of cancer trials at the Cross Cancer Institute. You will identify eligible participants, obtain consent, conduct visits, monitor safety, and assist with audits while collaborating with clinicians and study monitors. Provisions include potential...

Parexel FSP in Canada seeks a Clinical Research Manager to lead end-to-end study delivery in ICH/GCP environments, coordinating between Country Operations, the clinical trial team, and external partners. You will drive feasibility, site selection, recruitment, execution and closeout, mentoring local teams, ensuring CTMS/eTMF compliance, and balancing...

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...

Parexel is seeking a Study Operations Manager I to oversee study startups through closeout across one or more studies, with leadership for regional activities. The role emphasizes strategic planning, operational delivery, and cross-functional collaboration to support global trials. The SOM I will liaise with GSMs, pCROs, CTMs/SCPs, and regulatory colleagues...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...