Clinical Trials

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...

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...

**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...

**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,...

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...

**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**: -...

**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**: -...

Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. - Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any...

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...

393172BR **Clinical Research Medical Advisor**: India **About the role** Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe. Your responsibilities include, but are not...

Vasta Bio-Informatics Private LimitedMaharashtraPosted On - 04 Oct 2024 - Required Experience - 1 - 3 Years Basic SectionNo. Of Openings 1 Grade C1B Designation CLINICAL RESEARCH ASSOCIATE Closing Date 29 Nov 2024 - OrganisationalCountry IN State MAHARASHTRA City NAVI MUMBAI Location Navi Mumbai-I - SkillsSkill CLINICAL...

**Title**:Clinical Research Associate**: - Date: Sep 3, 2024- Location: Sun House - Corporate Office- Company: Sun Pharma Laboratories Ltd**In-House Managed Studies** - Site feasibility, potential investigator identification and development of study budgets for each study - Finalization of investigators, sites and execution of CDA and study related...

**In-House Managed Studies** - Site feasibility, potential investigator identification and development of study budgets for each study - Finalization of investigators, sites and execution of CDA and study related contracts - Plan and conduct Investigator’s Meeting if needed - Preparation and submission of study documents for EC permission for respective...

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 clinical research associate (CRA), you'll **run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use**. Pay: Up to ₹27,000.00 per month **Benefits**: - Health insurance - Provident Fund Schedule: - Day shift Supplemental Pay: - Yearly bonus Work Location: In person

**Responsibilities** - Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations - Serve as primary Sponsor contact for operational project-specific issues and study deliverables - Maintain in depth knowledge of protocol, therapeutic...

A minimum of 4+ years of experience as a trainer, teacher, or instructor in clinical research. Well versed with all the concepts of the Clinical operations with an experience of CRC or CRA. Providing Clinical Research Associates with project-specific training. Assuring compliance with SOPs and local regulations, and CFR, ICH, and GCP guidelines. Creating...

As a **Clinical SAS Programmer **you will Ssupport all programming activities which will required for the data analysis of the clinical trials and create standard datasets (SDTM) and analysis datasets (ADaM) and generate reports of the form Tables, Graphs and Listings as applicable. - Planning and working with the clinical programming group to schedule...