QA - Clinical Trials

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: ...

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...

**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...

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...

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:...

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...

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...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

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...

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...

**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...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...