THThepharmadaily
Clinical Research - Associate
Nagercoil ₹8-13 LPA Posted 13 Aug 2025
FULL TIME
Protocol Development
Clinical Trials
Data Analysis
Regulatory Compliance
patient recruitment
Job Description
- we're looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights
- Collaborating with cross-functional teams, you will contribute to the systematic review of medical literature, ensuring that our reports adhere to rigorous standards and regulatory guidelines
- Join us in our commitment to excellence within the realm of clinical research and literature analysis
Department - Research & Analysis
Skills Required - Data Validation
Role
- Conduct systematic literature reviews (SLR) and meta-analyses, including screening and extraction.
- Prepare training data for AI model development.
- Write clinical reports following regulatory guidelines.
- Ensure data accuracy and quality through thorough checks.
- Manage assigned projects, meet deadlines, and communicate progress.
- Summarize articles and create literature summaries.
- Utilize social media listening to identify patient-reported outcomes.
Education/Qualification - Any Lifesciences degree, including B. Pharm, D. Pharm, BioMedical Engineering, BioTechnology, Microbiology, etc