ICON plc is hiring for the position of Clinical Trial Assistant at their Bengaluru, Karnataka location. This role typically involves providing administrative support for clinical trials, assisting with documentation, coordinating with trial teams, and ensuring that clinical study activities are conducted in compliance with regulatory and company requirements.
Clinical Trial Assistant
Bengaluru, Karnataka, India
About the job
Clinical Trial Assistant- bangalore
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Clinical Trial Assistant to join our diverse and dynamic team. As a Clinical Trial Assistant you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What You Will Be Doing
- Keeping up to date with all the changes/required knowledge on ICH GCP.
- May be responsible for supporting multiple studies simultaneously and must prioritize appropriately to meet business needs to ensure delivery of results.
- Maintain all the study trackers and access
- Analysis of various reports
- Timely distribution of dashboards and reports to the study team
- Maintain all the study trackers and access
- Analysis of various reports
- Timely distribution of dashboards and reports to the study team
- Common email group to support the issues related to CSAP, CTMS
- Clinical admin support
- Support to studies where there is no requirement of SDS
- Work closely with SDS/SM to manage the activities post SAC and till final archival.
- Managing study systems
- TMF Management and Maintenance
- Managing TMF activities both for Inhouse and FSO trials
- Provide timely follow up with the stakeholders to improve the TMF compliance
Your profile
- Excellent technical/IT skills. Able to understand the impact of technology on studies and to use and develop computer skills.
- Knowledge of ICH GCP relevant operational procedures, systems, and quality guidelines regarding clinical studies
- Able to work independently as well as in a team.
- Professional attitude with good customer focus (internal and external)
- Time Management as system updates, eTMF etc. need to be done in a timely manner.
- Very good communication skills
- 1-2 years of prior experience in clinical operations