Full Time Jobs in Emelle September 2024

Overview: As a Study Delivery Lead, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   This position within GCD is accountable end to end from CSI (Commit to Study Initiation) until study archiving for planning and leading the delivery of interventional, studies to ti...

Overview: ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to acceler...

Overview: ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.   With our patients at the centre of all that we do, we help to acc...

Overview: As a Clinical Research Associate II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: The role of the Clinical Research Associate II is to ensure execution of clinical studies is conducted according to applicable requ...

Overview: As a CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: The role of the Clinical Research Associate II is to ensure execution of clinical studies is conducted according to applicable requirements, regulations, a...

Overview: As a  CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities in...

Overview:   The Site Activation Specialist is responsible for site start-up activities for the assigned studies within the Site Alliance and Site Activation Sub-Chapter under Clinical Operations. The position will require strong stakeholder management working closely with Contracting, IVDR, Legal, Privacy, Study Teams, CRO, and Sites.  Responsibi...

Overview: As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study p...

Overview: As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities inc...

Overview: As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities inc...