Clinical Trial Regulatory Affairs Professional

A Career at George Clinical offers you the opportunity to work with a dynamic team of professionals dedicated to advancing clinical research.As a Regulatory Specialist, you will be responsible for undertaking specific regulatory tasks required for the implementation of clinical trials.Your responsibilities will include:Maintaining current knowledge of...

Join to apply for the Clinical Trial Specialist role at George Clinical.At George Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device,...

Key ResponsibilitiesAs a Clinical Trial Specialist at George Clinical Pty, your key responsibilities will include:Conducting site feasibility assessments and coordinating site start-up activities.Managing TMFs and performing quality control checks on documents and emails.Preparing and participating in audit responses and ensuring compliance with regulatory...

Join to apply for the Regulatory Specialist role at George Clinical.At George Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and...

Unlock a rewarding career in clinical trials with George Clinical Pty.About the RoleThe Clinical Trial Specialist plays a vital role in ensuring the smooth execution of clinical trials. As part of the Clinical Operations team, you will be responsible for supporting site start-up and maintenance activities, working closely with project managers and clinical...

George Clinical Pty is a global Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region.We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.Our...

Job DescriptionAs a Research Operations Coordinator at George Clinical Pty, you will be responsible for supporting the planning and execution of clinical trials. Your key duties will include:Managing Trial Master Files (TMFs) to ensure compliance with regulatory requirements.Working closely with project teams to coordinate site start-up and maintenance...

Join Our Team at George Clinical, a global Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region.We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to...

About the RoleEli Lilly and Company is seeking a highly skilled Clinical Trial Associate Leader to join our team. In this role, you will be responsible for providing clinical trial capabilities in support of clinical development.You will ensure that investigator sites meet requirements to enroll study participants into clinical trials and support ongoing...

Job OverviewAssociate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with...

We are currently seeking Senior Clinical Trials Assistant (CTA) to join our sponsor-dedicated team in a client-facing role. As a vital part of our team, our CTAs perform daily administrative tasks to support clinical projects and update clinical systems and databases.You will also perform general administrative tasks as needed. You will have excellent...

Job DescriptionWe are currently seeking an experienced Senior Clinical Trials Assistant to support clinical projects and update clinical systems and databases.This role requires excellent communication, computer, and problem-solving skills, as well as being resourceful, analytical, adaptable, and organized.

Are you passionate about improving global health? As a Global Clinical Trials Professional at George Clinical Pty, you will have the opportunity to work on complex clinical trials, collaborating with cross-functional teams to deliver high-quality results.About the CompanyGeorge Clinical Pty is a global Contract Research Organization (CRO) with a rich...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Company Overview">IQVIA Argentina is a leading global contract research organization dedicated to advancing medical science and developing innovative solutions for the life sciences industry.We are seeking a highly skilled Senior Clinical Trials Assistant to join our sponsor-dedicated team in a client-facing role.

Head of Project Operations, APAC (Mandarin Speaker)Join to apply for the Head of Project Operations, APAC (Mandarin Speaker) role at George Clinical.At George Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific...

Job OverviewClinical Research Associates play a crucial role in ensuring the success of clinical trials by managing site relationships and ensuring compliance with regulatory requirements.In this role, you will be responsible for developing strong relationships with investigators and site staff, ensuring accurate and timely data collection, and resolving any...

Job Title:Regulatory Affairs ManagerAbout the Role:We are seeking a highly motivated Regulatory Affairs Manager to join our team. The successful candidate will be responsible for managing the local implementation of quality assurance (QA), safety, health & environmental (SHE) and registration (REG) policies and standards.Key Responsibilities:Manage...

Job OverviewWe are seeking a Head of Clinical Research Operations to join our team at George Clinical Pty. The successful candidate will have a strong background in clinical research operations and will be responsible for overseeing project delivery and clinical operations across the Asia-Pacific region.Key ResponsibilitiesTeam Leadership:Recruit, develop,...

Job DescriptionThe Project Delivery Manager APAC will be responsible for ensuring the successful delivery of clinical trials by leading and developing high-performing teams, allocating resources effectively, and maintaining compliance with regulatory requirements.Key ResponsibilitiesTeam Leadership:Recruit, develop, and manage project management and clinical...