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:...

Experience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...

Experience: 3+ years in clinical trial medical writing   Responsibilities:   Develop case report formats, protocol letters, and record forms essential for clinical trials. Prepare all necessary documentation for clinical trial initiation, execution, and completion. Conduct literature reviews and data analysis to support trial design and manuscript...

Experience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...

Clinical Trial Associate Mumbai or Vadadora, India (hybrid: 3 days office, 2 days home) Salary: Competitive + Benefits + Bonus If you are an agile, committed, and innovative clinical trial professional then we want to hear from you! Join us to help improve peoples' lives and make healthcare better for everyone! Why Pharmanovia? Pharmanovia...

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...

Experience: 3+ years in clinical trial medical writingResponsibilities:Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript development.Draft...

**Mumbai or Vadodara, India (hybrid: 3 days office, 2 days home)**: **Salary: Competitive + Benefits + Bonus**: If you are an agile, committed, and innovative clinical trial professional, then we want to hear from you! Join us to help improve peoples’ lives and make healthcare better for everyone! **Why Pharmanovia?**: Pharmanovia is a dynamic,...

**Roles & Responsibilities** - Conduct audits of clinical trail study - Conduct operations as per SOP - Conduct vendor audits - Maintain Quality system for clinical trial unit - Maintain relevant documentation **Criteria** Minimum of **2-5 years of experience** in pharmaceutical industry **Salary**: ₹35,000.00 - ₹58,000.00 per month Application...

SUMMARY As part of the ACM Clinical Trails Study Support team this role supports both the Project Team and Clinical Trials Investigator sites from study set up through to study close out. Acts as a member of the Project Team to support all ongoing studies with tasks as needed, as defined by the Project Team or ACM client. STATUS: Full Time LOCATION:...

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...

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...

Position Title: Local Trial Manager Position Summary: The Local Trial Manager is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The LTM is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s)...