QA - Clinical Trials

Clinical trials are the actual experimental studies in which human volunteers are included, after their consent, to test new treatments, instruments, Read More

As a Clinical Trial Assistant (CTA) at [Company Name], you will play a crucial role in supporting the successful execution of clinical trials. Working closely with the clinical operations team, you will provide administrative and operational assistance to ensure the smooth conduct of trials from initiation to closeout. **Key Responsibilities**: - Maintain...

**Vadodara or Mumbai, 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,...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Clinical trials are the actual experimental studies in which human volunteers are included, after their consent, to test new treatments, instruments,Read More

ICON plc is a leading healthcare intelligence and clinical research company. We take pride in creating a diverse and innovative work environment, and we invite you to be part of our journey to influence the future of clinical development.Clinical Trial AssistantLocation : Mumbai, On-siteResponsibilities:- Document collection and submission support- Vendor...

**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,...

**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,...

all Clinical Research Topic: - DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 1 DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 2 THE EVALUTION OF THE CLINICAL TRIAL PROCESS-A BRIEF HISTORY LESSON HISTORICAL BACKGROUND OF GCPINSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC)STAKEHOLDERS ENGAGEMENT TO ENSURE A SUCCESSFUL TRIAL...

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...

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 is...

We are looking for a skilled Clinical Trial Medical Writer!Experience: 3+ years working in the field of clinical trial medical writingDevelop case report formats, protocol letters, and record forms crucial for clinical trialsPrepare all required documentation for the initiation, execution, and completion of clinical trialsConduct literature reviews and...

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...

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...

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...

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...