
Centralized Trip Report Reviewer-i
7 days ago
Management of projects under direction of a Project Manager / Director as assigned.
- Ensure site monitoring responsibility for clinical studies are conducted according to Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation of Initiatives either independently or with team)
- Proactively identify opportunities for process improvements and work collaboratively with project team incase further action required
- Complete required trainings according to required timelines.
- Follow applicable departmental Standard Operating Procedures and Work Instructions
- Follow project issue escalation process and Corrective Action Issue Resolution (CAIR) process for clinical operations issues
- Ensure follow up on issues and risks and protocol deviations and to be a liaison between CRA, CTL and PM for timely resolution of issues
- Responsible for the timely and appropriate communication to the clinical operations team Liaise with CTL/PM to communicate any trends, outstanding issues, safety concerns or any other activity or lack thereof which may jeopardize the clinical trial delivery or patient safety.
- Review progress of project and initiate appropriate actions to achieve target objectives assigned.
- Support in review of Standard Operating Procedures or Work Instructions to align with process or tool modifications
- Other duties as assigned by management: Ex: Document Review, ETMF reconciliation, other CTL tasks etc.
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Centralized Trip Report Reviewer
7 hours ago
Bengaluru, India Labcorp Full timeManagement of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Labcorp Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation...
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Centralized Study Spec I
1 week ago
Bengaluru, Karnataka, India Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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Central Operations Executive
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Centralized Visit Report Reviewer Ii
7 days ago
Bengaluru, Karnataka, India Precision for Medicine Full time**Job Summary**: The Centralized Visit Report Reviewer II serves as a member of a project team reviewing and approving site monitoring visit reports. Leveraging their experience, the CVRR II works with some oversight, and managing report review and issue escalation for a range of studies and/or portfolios of work. **Essential Job Functions**: - Performs...
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Central Operations Executive
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Reporting Associate I
7 hours ago
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Centralised Clinical Team Lead II
2 weeks ago
Bengaluru, Karnataka, India Fortrea Full time ₹ 9,00,000 - ₹ 12,00,000 per year.Individual ContributorTrip Report Review responsibilities: Reviews trip reports and works closely with project teams towards implementation of best trip report practices; revising applicable project plans where needed. Proactively identifies risks in the trip reports and communicates any trends, outstanding issues, safety concerns to the study team. Ensures...
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Centralised Clinical Team Lead II
2 days ago
Bengaluru, Karnataka, India Fortrea Full time ₹ 9,00,000 - ₹ 12,00,000 per year. Individual Contributor Trip Report Review responsibilities: Reviews trip reports and works closely with project teams towards implementation of best trip report practices; revising applicable project plans where needed. Proactively identifies risks in the trip reports and communicates any trends, outstanding issues, safety concerns to the study team....