Company Description Trialenta – Clinical Research Jobs & Recruitment Community – is a clinical research career and talent platform that helps aspiring professionals build job-ready skills, understand industry pathways, and connect with relevant opportunities. The community supports students and early-career talent from life sciences, pharmacy, biotechnology, nursing, and related disciplines aiming for roles such as Clinical Research Associate, Clinical Operations, Pharmacovigilance, Regulatory Affairs, Clinical Data Management, Medical Writing, and Drug Safety. Trialenta offers clear career roadmaps, practical guidance on CVs and interviews, skill development support, and insights into industry trends and the talent market. Its transparent, consent-based talent community is designed to ethically prepare and connect motivated individuals with real opportunities, without guaranteeing jobs or charging for placements. The mission is to help clinical research aspirants turn their potential into meaningful, sustainable careers in the industry. Role Description The Clinical Operations Specialist is a full-time, on-site role based in Delhi, India. This role involves coordinating and overseeing day-to-day clinical trial activities, including site communication, visit tracking, and adherence to study timelines and quality standards. The specialist will support protocol implementation, maintain study documentation, assist in feasibility assessments, and help ensure compliance with regulatory and ethical requirements.



Responsibilities include collaborating with cross-functional teams, monitoring operational performance metrics, identifying risks or deviations, and contributing to continuous process improvements. The role also includes supporting training for sites or junior team members and contributing operational insights to Trialenta’s broader community and content initiatives. Qualifications
• Strong foundation in clinical operations and clinical trials, with practical understanding of trial workflows and site coordination.
• Experience in research activities, including data collection, documentation, and adherence to Good Clinical Practice (GCP) and relevant guidelines.
• Project management skills to plan, prioritize, and track clinical activities, manage timelines, and coordinate with internal and external stakeholders.
• Ability to interpret and apply study protocols, ensuring operational alignment with protocol requirements and compliance standards.
• Bachelor’s or master’s degree in life sciences, pharmacy, biotechnology, nursing, or a related field.
• Strong attention to detail, analytical thinking, and problem-solving abilities in a regulated setting.
• Clear written and verbal communication skills, with the ability to collaborate across multidisciplinary teams.
• Familiarity with clinical research regulations, ethics committees, and documentation practices; prior experience in clinical operations or trial coordination is an advantage.

📌 Clinical Operations Specialist (India)
🏢 Trialenta - Clinical Research Jobs & Recruitment Community
📍 India