Clinical Trial Assistant

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...

**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...

**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...

We are seeking an experienced Senior Statistical Programmer to join our team and contribute to the development of clinical trials. This role involves working with SAS and other software to create custom programming code, ensuring high-quality outputs, and leading a team of programmers to deliver projects on time.Key Responsibilities:Develop and maintain...

**Key Responsibilities**: **1. Clinical Trial & Evaluation Management** Ø Support planning, coordination, and monitoring of clinical trials/studies for medical devices. Ø Ensure compliance with ISO 13485 requirements. Ø Assist in the preparation of clinical evaluation reports (CER) as per MEDDEV 2.7/1 Rev. 4 and EU MDR. Ø Coordinate site selection,...

Assist in setting up, monitoring, and closing clinical trial sites under supervision. - Ensure trials are conducted in accordance with ICH-GCP guidelines, regulatory requirements, and company SOPs. - Review case report forms (CRFs) for completeness, accuracy, and consistency. - Assist with study documentation including investigator site files (ISFs), trial...

**Position** This role involves coordinating clinical trials, ensuring compliance with ICH-GCP guidelines, and working closely with investigators, sponsors, and regulatory bodies to conduct high-quality research. **Key Responsibilities** - Coordinate with Principal Investigators (PIs), Institutional Review Boards (IRB), Sponsors/CROs, and research teams to...

Pacifix Research is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. This is an excellent opportunity for fresh graduates interested in starting their career in clinical research. The Clinical Research Coordinator will play a crucial role in coordinating and managing clinical trials, ensuring compliance with regulatory...

Vasta Bio-Informatics Private LimitedMaharashtraPosted On - 19 Sep 2024 - Required Experience - 1 - 3 Years Basic SectionNo. Of Openings 5 Grade C1B Designation CLINICAL RESEARCH ASSOCIATE Closing Date 16 Jan 2025 - OrganisationalCountry IN State MAHARASHTRA City NAVI MUMBAI Location Navi Mumbai-I - SkillsSkill CLINICAL...