Clinical Study Project Manager

Job PurposeThis position entails overseeing project management and study site management from site selection to initiation, monitoring, and close-out of assigned clinical studies in accordance with applicable regulations.Key ResponsibilitiesConduct thorough site selection assessmentsCoordinate with cross-functional teams to ensure seamless study...

**Who are we?**We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980's. If you already work in this industry you'll know that we are experts in our field.**Why...

EmployeeFull timeAbout the Company:BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160; SHA: 688235) is a global, commercial-stage, research-based biotechnology company focused on molecularly-targeted and immuno-oncology cancer therapeutics. With a team of over 9,500 employees across the United States, China, Europe and Asia Pacific region, BeiGene is advancing a...

Clinical Research Associate Job Summary">Key Responsibilities:Develop and execute clinical study protocols, case report forms (CRFs), annual reports, and other study materials.Conduct site assessments to identify and select suitable investigator sites for clinical studies.Responsible for all site monitoring, including routine monitoring and close-out of...

**Core Responsibilities**- Organise project systems set-up during the initiation phase.- Draft Kick-Off Meeting materials & liaise with all stakeholders to facilitate the meeting.- Draft project plans for review by the Clinical Project Manager (CPM).- Maintain project information in the Clinical Trial Management System (CTMS), including project milestone...

Job OverviewThe role of a Clinical Research Associate involves working directly with sponsors to conduct monitoring activities across various trials in a remote or on-site hybrid setting.Key Responsibilities:Ensure compliance with ICH-GCP and local regulations by maintaining accurate documentation and procedural records.Monitor and manage study sites,...

**Project Associate | Office based (Sydney, Melbourne or Adelaide)*****Who are we?**We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980's. If you already work in...

Clinical Research Associate PositionAs a Clinical Research Associate, you will play a vital role in ensuring the conduct of clinical studies is in compliance with regulatory requirements and high-quality standards. This position offers individualized solutions tailored to meet the needs of our clients.Main ResponsibilitiesEnsure study protocol compliance...

Clinical Research Assistants play a vital role in the coordination of clinical research projects, working closely with researchers and healthcare professionals to ensure the success of these studies. In this dynamic position, you will be responsible for coordinating participant recruitment, collecting data, handling biological specimens, managing records,...

Senior Clinical Research Associate Job DescriptionThe primary role of a Senior Clinical Research Associate is to oversee the implementation and conduct of clinical studies at participating sites. This involves assessing site qualifications, managing site conduct, ensuring site performance and quality, and closing out studies.This position requires strong...