Clinical Trial Project Coordinator

In this role, you will play a critical part in the success of our clinical trials.Job DescriptionAs a Clinical Research Associate, you will be responsible for managing clinical trials from start-up to close out.You will work closely with investigators and site staff to ensure that studies are implemented according to protocol.You will assess and ensure...

Join Our TeamWe are seeking a highly motivated Clinical Trials Manager to join our team at Syneos Health, Inc. In this role, you will be responsible for coordinating communications between study team stakeholders and global teams of site-facing site contract & budget negotiators.Your Key ResponsibilitiesClinical Study Agreements: Collaborate with global...

About the RoleWe're searching for a knowledgeable, team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Malaysia. You will work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications.The successful candidate will maintain the...

We are a mature and experienced Contract Research Organization (CRO) with a strong presence in the global clinical research industry. Our company has grown organically from a handful of countries to a global presence, while maintaining our independence and freedom to operate.Job ResponsibilitiesWe are seeking a skilled Senior Clinical Research Associate to...

Clinical Trial Administrator RoleWe are seeking a highly motivated and organized Clinical Trial Administrator to join our team. This individual will be responsible for coordinating and executing various aspects of clinical trials, including document management, tracking systems, and vendor liaison.

Job OverviewWe are looking for a skilled Clinical Research Associate to join our team in Malaysia.The successful candidate will be responsible for managing the clinical aspects of full-service global projects.Main Responsibilities:Supervise study activities, timelines, milestones, and schedules on the country level.Conduct and report all types of onsite...

About the RoleWe are seeking a highly organized and detail-oriented Clinical Trial Administrator to join our team. As a key member of our Clinical Project Team, this individual will be responsible for coordinating and executing various aspects of clinical trials.

Job OpportunityWe're searching for a qualified Research Associate to oversee the clinical aspects of global projects in Malaysia.About the Position:Manage the clinical aspects of full-service global projects in Malaysia.Supervise study activities, timelines, milestones, and schedules on the country level.Conduct and report all types of onsite monitoring...

Job SummaryWe are seeking a highly skilled Site Activation Manager to join our clinical Functional Service Provider (cFSP) team at IQVIA Argentina.Key Responsibilities:Site Activation and Maintenance: Direct and manage the delivery of site activation, maintenance, and regulatory activities for assigned projects in accordance with the agreed scope of work and...

We are a dynamic and global Contract Research Organization (CRO) committed to delivering high-quality clinical research services. Our company has grown organically from a handful of countries to a global presence, while maintaining our independence and freedom to operate.Job RequirementsWe are looking for a knowledgeable and team-oriented Senior Clinical...

This role requires a high degree of autonomy, with ability to work independently and make decisions in a fast-paced environment.Job DescriptionAs a Clinical Research Associate, you will be responsible for managing clinical trials from start-up to close out.You will work closely with investigators and site staff to ensure that studies are implemented...

Job OverviewWe are seeking a seasoned Senior Clinical Research Associate to join our team in Malaysia. As a key member of our global clinical operations team, you will be responsible for managing the clinical aspects of full-service global projects.The ideal candidate will have extensive experience in conducting all types of monitoring visits in Phase II...

As a key member of our team, you will be responsible for ensuring the highest standards of clinical quality compliance in our organisation. This involves serving as a local expert on ICH-GCP and local regulations, conducting impact assessments to identify areas for improvement, and developing effective solutions to ensure compliance.You will work closely...

Job SummaryThe Clinical Trial Administrator is responsible for performing study-related tasks and ensuring timely production of high-quality clinical data. This individual will work closely with the project team to ensure successful execution of clinical research projects.Main Duties:Document and track study activities using relevant forms and tools.Assist...

We are seeking an experienced Compliance Lead to join our Clinical Research Operations team. As a key member of our team, you will be responsible for ensuring the highest standards of clinical quality compliance across our global operations. This will involve working closely with local country operations management to develop and implement effective...

Job DescriptionWe're seeking an experienced Senior Clinical Research Associate to manage the clinical aspects of full-service global projects in Malaysia.About the Role:Supervise study activities, timelines, milestones, and schedules on the country level.Conduct and report all types of onsite monitoring visits.Be involved in study set-up, including site...

Parexel Federal Territory of Kuala Lumpur, MalaysiaClinical Research Associate - FSPParexel Federal Territory of Kuala Lumpur, MalaysiaKey Accountabilities:Start-up (from site identification through pre-initiation):Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.Build relationships...

Parexel is a leading global biopharmaceutical services company.Clinical Research Associate Job DescriptionAs a Clinical Research Associate, you will be responsible for managing clinical trials from site identification to close out.You will act as Parexel's direct point of contact with assigned sites, assessing and ensuring overall integrity of study...

About the RoleWe are seeking a highly skilled Senior Clinical Contracts Specialist to join our team at Syneos Health, Inc. In this role, you will be responsible for establishing and maintaining training material for site contracts lead team and site contract negotiators.Your Key ResponsibilitiesNegotiate Clinical Study Agreements (CTAs): Collaborate with...

Key ResponsibilitiesAs a Clinical Research Operations Lead at IQVIA, you will be responsible for directing and managing the delivery of site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs. Your key responsibilities will include overseeing the execution of site activation, developing and implementing...