Clinical Research Associate

About the RoleWe are seeking a Senior Clinical Research Associate to join our IQVIA Argentina team. As a key member of our team, you will be responsible for conducting site visits, adapting and driving subject recruitment plans, and administering protocol training.You will evaluate the quality and integrity of study site practices and manage the progress of...

Job OverviewIQVIA Argentina is seeking a highly skilled Senior Clinical Research Associate to join our team. The ideal candidate will have extensive experience in clinical research and a proven track record of conducting monitoring and site management work.Conduct site visits to ensure that sites are conducting studies and reporting data as required by the...

Job SummaryIQVIA Argentina is looking for a Senior Clinical Research Associate to perform monitoring and site management work. The successful candidate will have a strong background in clinical research and excellent communication skills.Monitoring and site management responsibilities include conducting site visits, adapting and driving subject recruitment...

Clinical Data Associate - Hybrid (Bloemfontein)Apply locations: Bloemfontein, South Africa; Cape Town, Western Cape, South Africa; Centurion, South AfricaTime type: Full timePosted on: Posted YesterdayTime left to apply: End Date: May 1, 2025 (30+ days left to apply)Job requisition id: R1468141Base level rolePerform comprehensive data management tasks...

Clinical Data Associates at IQVIA LLC are responsible for ensuring the integrity and quality of clinical data. Key responsibilities include data review, query generation, data reconciliation, and study closeout activities.Required Skills and Qualifications:Bachelor's degree in a Health or Science discipline with experience in clinical research.Data...

Job DescriptionIQVIA Argentina is seeking a Senior Clinical Research Associate to join our team. The ideal candidate will have extensive experience in clinical research and a proven track record of conducting monitoring and site management work.The role involves conducting site visits, adapting and driving subject recruitment plans, and administering...

Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up, Execution,...

Role Summary:A Clinical Research Specialist is needed to drive site activation and customer experience across the globe.This individual will review documents for completeness and accuracy, prepare site regulatory documents, and track document progress, approval, and execution.In this role, you will be responsible for reviewing regulatory documents,...

Job DescriptionWe are seeking a highly skilled Clinical Data Associate to join our team. As a key member of our clinical operations group, you will be responsible for performing comprehensive data management tasks including data review, query generation and query resolution.This role may also include creation of eCRF completion guidelines, entry of test data...

Job DescriptionWe're looking for a skilled Clinical Research Recruitment Specialist to support our DSSM Talent Acquisition team at IQVIA. This role offers flexibility, allowing you to work remotely from anywhere in South Africa or split your time between home and our offices. As a Clinical Research Recruitment Specialist, you'll contribute to improving our...

BenefitsClinical Data Associates at IQVIA LLC enjoy a range of benefits, including professional growth opportunities, competitive compensation, and a dynamic work environment.Key Responsibilities:Data Review and Query GenerationData Reconciliation and ValidationStudy Meetings and TeleconferencesStudy Closeout and Archiving Activities

Key ResponsibilitiesPerform feasibility, site activation, and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions.Work closely with the Site Activation Manager, Project Management team, and other departments as necessary to ensure successful site activation.BenefitsExposure...

Job DescriptionIQVIA LLC seeks highly motivated Clinical Data Associates to join our team. As a Clinical Data Associate, you will be responsible for managing clinical data from study start-up to close-out.Key Responsibilities:Data Review and Query GenerationData Reconciliation and ValidationStudy Meetings and TeleconferencesStudy Closeout and Archiving...

Clinical Data Management Project LeadIQVIA is a global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We're seeking an experienced Clinical Data Management Project Lead to join our team.Job Summary:You will be responsible for managing end-to-end delivery of data management services for...

Job Description:A Research Site Coordinator is needed to perform tasks associated with site activation activities at the country level.The successful candidate will review documents for completeness, consistency, and accuracy, under guidance of senior staff, and prepare site regulatory documents.You will be responsible for reviewing regulatory, ethics, and...

Key ResponsibilitiesThe successful candidate will have a Bachelor's degree in a Health or Science discipline with experience in clinical research. They will also have data management experience and experience working on a clinical trial.Apart from this, the ideal candidate will have experience working in highly diverse teams within clinical research;...

Job OverviewHome-based in South AfricaThe Clinical Data Coder will manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer's satisfaction; provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs; provide leadership to the team in the...

Job title : Director: Monitoring and Institutional ResearchJob Location : Free State, BloemfonteinDeadline : March 14, 2025Quick Recommended LinksJobs by Location Job by industries Duties and responsibilities Leadership: Provide leadership and support to the University's strategic and institutional planning processes and activities.  Oversee the...

Company OverviewIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.Job DescriptionAs a Senior Site Activation Coordinator, you will perform tasks at a country level associated with site activation activities in accordance with applicable local...

KINDLY TAKE NOTE: Applications may only be submitted online through the official UFS vacancy website: - Applications submitted through any other platform will not be considered. Duties and responsibilities: Teach Public Policy and Public Administration modules to undergraduate and postgraduate students. Perform academic administration of undergraduate and...