Clinical Operations Specialist
Trialenta - Clinical Research Jobs & Recruitment Community
Delhi, India4h agovia LinkedIn
About the Role
The Clinical Operations Specialist is a full-time, on-site role based in Delhi, India.
Key Responsibilities
- Coordinate and oversee day-to-day clinical trial activities.
- Manage site communication.
- Track site visits.
- Ensure adherence to study timelines and quality standards.
- Support protocol implementation.
- Maintain study documentation.
- Assist in feasibility assessments.
- Ensure compliance with regulatory and ethical requirements.
- Collaborate with cross-functional teams.
- Monitor operational performance metrics.
- Identify risks or deviations.
- Contribute to continuous process improvements.
- Support training for sites or junior team members.
- Contribute operational insights to Trialenta’s broader community and content initiatives.
Requirements & Tech Stack
- 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.
- Strong attention to detail, analytical thinking, and problem-solving abilities in a regulated environment.
- Clear written and verbal communication skills, with the ability to collaborate across multidisciplinary teams.
- Familiarity with clinical research regulations, ethics committees, and documentation practices.
Qualifications
- Bachelor’s or master’s degree in life sciences, pharmacy, biotechnology, nursing, or a related field.
- Prior experience in clinical operations or trial coordination is an advantage.