Posted:3 hours ago|
Platform:
Work from Office
Full Time
Research Analyst - II Roles & Responsibilities: To perform Secondary research in order to provide the detailed information or the complete profile of the product. Thorough understanding of regulations, Ability to grasp new concepts quickly and to assimilate and evaluate scientific data keeping up to date with changes in regulatory legislation and guidelines Strong secondary research skills and Sound Knowledge on drug labels and clinical trial Knowledge on drugs, devices and other products regulations Able to evaluate applicable laws and regulations to determine impact & Able to mentor team members Compile and analyze data using modern and traditional methods to collect it. Responsible for conducting intelligence research & analysis on public, biotech and pharma companies and universities related to drug research and development. Capturing data on companies developing drugs, devices, their descriptions, clinical trial information from press releases, annual reports, quarter and half year reports, sec filings, company websites, clinical trial reports, NIH reports and updating scientific information. 1. Top primary skills required for this role:- Knowledge on Regulatory Affairs, Sound knowledge on all aspects of product development, including research, clinical trials, manufacturing practices, regulations, and approval processes. 2. Secondary skills required for this role:- Secondary Research. Knowledge on drugs and clinical trials. 3. Tertiary skills required for this role:- Analytical Knowledge & Scientific terminology. Eligibility Criteria: 1-3 Years of experience Education any UG/PG in Life Sciences. Strong Knowledge and skills on Scientific Terminology, Secondary Search, Regulatory Bodies (likely Medical Devices) & Clinical Trials also QC/Quality Checks
Makro Group
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