Clinical Trial Assistant

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 is committed to providing cancer treatments of the future to the world of today. TRIO’s head office is in Edmonton, Alberta, Canada with operations all...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved in data...

We are looking for a compassionate and experienced Pediatric Nurse or Neontal Nurse for Clinical Trial to perform home visits for new mothers and their babies who are participating in a clinical trial. The visits/hours can be arranged to suit your current work schedule and the weekly working hours will depend on patient visits. **Locations:...

General Description/Scope of Responsibilities (Internship): - Support project/study activities and interact with project/study teams to ensure that all data, documentation, and information required fully align with study targets - Creating / refreshing / updating / maintaining assigned SharePoint folders - Support maintenance of the electronic Trial Master...

The Clinical Project Manager’s responsibilities include operational delivery of strategic clinical studies assigned to the country, to support the sponsor’s pipeline, in accordance with ICH/GCP, SOPs, local operating guidelines and local requirements, as applicable. The Clinical Project Manager works locally, supporting Associate Director Clinical...

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Ensures clinical study sites are conducting clinical trials in compliance with the respective protocol, SOPs and applicable ICH/GCP guidelines and regulations -...

**Description** **CRA, sponsor dedicated, full-time, permanent, home-based role, in Switzerland (we are flexible to adjust the level of the role to your experience) - fluent EN, DE and FR required** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product...

**Description** **Principal Medical Writer** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

**Description** **Clinical Research Associate** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...