Centralized Study Associate 1
4 days ago
Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day-to-day tasks ensuring quality and productivity. Maintain project and technical documentation in an appropriate manner. Perform checks to ensure quality of work completed Ensure timely escalation as needed. Assist in the document management (including document template creation, collection, review, processing and tracking up to eTMF filing) for all documents in the scope of agreed processes/activities or within the scope of GSDM throughout the study duration. Assist in the preparation of new investigator submission packages for site/regulatory submission. Assist in Investigator Payment Processing Assist the study start up teams with tasks required for site start up activities. Other duties/activities as assigned by study management team, but not limited to:
- Manage clinical systems & access management
- Manage study documents such as study level, country level and site level
- Maintain study databases (CTMS, IWRS, EDC etc.)
- Support study team in e-TMF management activities
- Support study team in data review and support activities.
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Centralized Study Associate Ii
2 days ago
Bengaluru, India Labcorp Full timeCentralized Study Associate II - To complete Other duties/activities as assigned by study management team, but not limited to: Ø Manage clinical systems & access management - Maintain study databases (CTMS, IWRS, EDC etc.) - Support study team in e-TMF management activities - Support study team in data review and support activities. - Support in generating...
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Centralized Study Spec I
2 weeks 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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Study Start Up Associate 1
2 days ago
Bengaluru, India Icon plc Full timeSite Management Associate 1 (SMA) JR090046 Site: Mexico or Colombia At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals...
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Centralized Study Associate I
2 weeks ago
Bengaluru, India Labcorp Full timeManage study documents such as study level, country level and site level - Maintain study databases (CTMS, IWRS, EDC etc.) - Support study team in e-TMF management activities - Support study team in data review and support activities - Upload, check, correct and maintain study documents for document review in the study eTMF regionally. - Send study documents...
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Senior Central Monitor
3 weeks ago
Bengaluru, India Precision For Medicine Full timePosition Summary The Senior Central Monitor will play a key role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development of Risk-Based Quality Management (RBQM) plans, conducting study risk assessments,...
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Senior Central Monitor
2 weeks ago
Bengaluru, India Precision For Medicine Full timePosition SummaryThe Senior Central Monitor will play a key role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development of Risk-Based Quality Management (RBQM) plans, conducting study risk assessments,...
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Senior Central Monitor
1 week ago
Bengaluru, India Precision For Medicine Full timePosition SummaryThe Senior Central Monitor will play a key role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development of Risk-Based Quality Management (RBQM) plans, conducting study risk assessments,...
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Senior central monitor
2 weeks ago
Bengaluru, India Precision For Medicine Full timePosition SummaryThe Senior Central Monitor will play a key role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development of Risk-Based Quality Management (RBQM) plans, conducting study risk assessments,...
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Centralized Study Associate 2
6 days ago
Bengaluru, India Labcorp Full timeFollow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day-to-day tasks ensuring quality and productivity. Manage project and technical documentation in an appropriate manner. Provide administrative and technical support to internal departments and teams as...
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Principal Central Monitor
3 weeks ago
Bengaluru, India Precision Medicine Group Full timePosition Summary The Principal Central Monitor serves as a strategic leader in driving data integrity, patient safety, and operational excellence across clinical development programs through advanced centralized monitoring and risk-based quality management (RBQM). This role is accountable for shaping and executing enterprise-wide RBQM strategies, leading...
