Back
Tier-1 brand and metro Chennai increase applicant density despite clinical specialization.
Requires clinical trial and GCP expertise, limiting direct transferability across industries.
Mandatory GCP, regulatory knowledge and system experience create moderate shortlisting filters without years requirement.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Conduct data monitoring and management including data review, query management, and investigating logic check flags in clinical trials.
Ensure quality of clinical database design via documentation, testing, validation, and implementation of clinical data collection tools or systems.
Serve as first point of contact for Clinical Trial Management System (CTMS) related questions and collaborate to resolve document discrepancies with study and document owners.
BA/BS degree with any years of experience.
Experience with ICH/GCP documentation requirements.
Hands-on experience using electronic documentation management and/or web-based data management systems.
Strong understanding of clinical development process and regulatory requirements, with effective English communication skills.
Experience using clinical trial management systems (CTMS) and familiarity with data validation and quality control processes.
Ability to work collaboratively and contribute to process improvements.
Experience using AI tools (e.g., ChatGPT, Microsoft Copilot) to enhance problem solving and productivity, along with understanding responsible AI practices.