Clinical Research Associate

JOB DETAILS 1 Performing routine data collection from patients,2 Verifying data sources, and reviewing regulatory documents/files to ensure that documents are in compliance with protocols, regulatory requirement 3 SOPs (standard operating procedures), and are aligned with the Monitoring Plan. 4 Some clinical research associates assist in reviewing study...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee...

Location: Noida **Roles and Responsibilities** - Primary Research to gather global News like, Plant shut-down, up-coming projects of all PSUs and Manufacturers in Metallurgy department, Government Initiatives, Policy, and Regulatory updates etc. - Tracking price trend/movement of raw materials on real-time basis. - Conducting Primary Research with...

Job Title: Research AnalystIndustry - Market ResearchKey Responsibilities:Taking/ Answering calls and collect opinion of US based respondents as per the project assignedNeed to take care of data collection services and adhere to company policiesNeed to maintain professionalism & telephonic etiquettesNeed to maintain individual performance report and share it...

Research Associates / Sr. Associates, BGV Associates / Sr. Associates, Study Abroad Associates / Sr. Associates. Background Verification (BGV)background screening or employee verification

JOB DETAILS 1 To provide timely inputs in the protocol and Informed Consent (for e.g. dosing information, contraindications, warnings, precautions, adverse events, and drug interactions) and thus ensure it is scientifically sound and gives a clear detailed description of trial related activities.2 To submit protocol and other required study related documents...

JOB DETAILS 1 To provide timely inputs in the protocol and Informed Consent (for e.g. dosing information, contraindications, warnings, precautions, adverse events, and drug interactions) and thus ensure it is scientifically sound and gives a clear detailed description of trial related activities.2 To submit protocol and other required study related documents...

We are looking for an Associate Analyst to join our Life Science and Healthcare Products business group in Noida. This is an amazing opportunity to be a member of a talented and vibrant Biopharma Insights team. The team consists of about 100 people and is reporting to the Director/Senior Director. We have a great skill set in market research and assessment,...

**What will you be doing in this role?** The person will be responsible to conduct secondary market research including gathering data from various proprietary and publicly available resources (e.g., brokerage reports, scientific and clinical publications, company press releases, investor reports, conference abstracts, company websites); prepare complete...