Clinical Trial Assistant

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Clinical Trial AssistantLocation : Mumbai, Office basedResponsibilities:What you will be doing: ...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Clinical Trial AssistantLocation : Mumbai, Office basedResponsibilities:What you will be doing:...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Clinical Trial AssistantLocation : Mumbai, Office basedResponsibilities:What you will be doing:...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Clinical Trial Assistant Location : Mumbai, Office based Responsibilities: What you will be...

Responsible for writing and managing protocols, recruitment, patient screening, patient consent forms and follow up management with Investigator. - Maintain source documentation and drug accountability, AE/SAEs reporting, maintaining site master file. - Site monitoring, Inspection, Audit etc. - **Development of study documents for and Management of...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Clinical Trial AssistantLocation : Mumbai, Office basedResponsibilities:- What you will be doing:...

**Essential Job Duties**: 1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support 2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs 3) Complete minute taking and documentation for sponsor/external or internal teleconferences...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

105,000 people reimagining medicine for more than 766 million people globally. To provide country clinical strategic guidance and feasibility assessment for GDD trials. Your responsibilities include, but are not limited to - To provide clinical strategic and tactical leadership in the country to support GDD trials, clinical development plans which change the...

To monitor clinical trials in various Hospitals. - Coordinate with the Hospital staff for pre - clinical reports. - Ensure proper execution of clinical protocols in the hospitals. - Analyse statistical data generated from the clinical trials. - Prepare report and articles based on the data analysis. - Submit clinical trial documents to the ethics committee...

Role Overview :The Clinical Development incumbent will be responsible for the oversight of development and execution linked to worldwide clinical development plans for the assigned programs in portfolio focussed on Oncology and innovative in-licensed assets. The incumbent will be responsible for integrating clinical development objectives with global...

**JD of Quality Assurance** **General Information** **Designation: Quality Assurance** **Status: Full-time** - In depth knowledge regarding Clinical trial processes, drug discovery life cycle, and computer systems used in clinical Sciences. - Ability to understand life sciences and healthcare regulatory reporting and compliance. - Experience in working on...

**JD of Quality Assurance** **General Information** **Designation: Quality Assurance** **Status: Full-time** - In depth knowledge regarding Clinical trial processes, drug discovery life cycle, and computer systems used in clinical Sciences. - Ability to understand life sciences and healthcare regulatory reporting and compliance. - Experience in working on...

Role Overview : The Clinical Development incumbent will be responsible for the oversight of development and execution linked to worldwide clinical development plans for the assigned programs in portfolio focussed on Oncology and innovative in-licensed assets. The incumbent will be responsible for integrating clinical development objectives with global...

Role Overview : The Clinical Development incumbent will be responsible for the oversight of development and execution linked to worldwide clinical development plans for the assigned programs in portfolio focussed on Oncology and innovative in-licensed assets. The incumbent will be responsible for integrating clinical development objectives with global...