Centralized Study Asso Ii
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. Manage project and technical documentation in an appropriate manner. Provide administrative and technical support to internal departments and teams as needed. Perform checks to ensure quality of work completed. Ensure timely escalation and issue resolution as needed. Track and report metrics as determined by management according to required timelines. Assist with the implementation of revised processes and procedures. 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. Review, Support, Manage or assist in Managing the site clinical trial contracts in accordance with defined processes and timelines Other duties/activities as assigned by study management team, but not limited to:
- 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 the study specific reports.
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement.
-
Centralized Study Asso Ii
13 hours 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...
-
Centralized Study Associate Ii
5 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...
-
Centralized Study Asso I
3 days ago
Bengaluru, India Labcorp Full time1. Follow all applicable departmental Standard Operating Procedures and Work Instructions. 2. Complete required trainings according to required timelines. 3. Complete day-to-day tasks ensuring quality and productivity. 4. Maintain project and technical documentation in an appropriate manner. 5. Perform checks to ensure quality of work completed 6. Ensure...
-
Centralized Study Asso I
3 months 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...
-
Centralized Study Spec Ii
4 months 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...
-
Centralised Study Asso Ii
3 months 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. Conducting operations in...
-
Centralized Study Spec I
4 months 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...
-
Centralized Study Spec I
2 months 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. Conducting operations in...
-
Centralized Study Assoc Ii
5 days ago
Bengaluru, India Labcorp Full timeSupport the payment of assigned studies which could include study set-up, maintenance, timely and accurate payment to the sites, as well as issue resolution and study reconciliation. Provide excellent customer service and site issue resolution Assist in setting entering study budgets and payees Review Electronic Data Capture updates and determine when...
-
Centralized Study Assoc Ii
7 months ago
Bengaluru, India Fortrea Full timeSupport the payment of assigned studies which could include study set-up, maintenance, timely and accurate payment to the sites, as well as issue resolution and study reconciliation. Provide excellent customer service and site issue resolution Assist in setting entering study budgets and payees Review Electronic Data Capture updates and determine when...
-
Centralized Study Associate Ii
7 months ago
Bengaluru, India Fortrea 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...
-
Centralized Study Associate Ii
6 months 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...
-
Study Start Up Associate Ii
4 weeks ago
Bengaluru, Karnataka, India ICON Plc Full timeStudy Start-Up Associate-II 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 Study Start Up Associate II to join our...
-
Study Start Up Associate Ii
7 months ago
Bengaluru, Karnataka, India ICON plc Full time**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 and set us apart as an organisation: Accountability & Delivery,...
-
Study Start Up Associate Ii
4 months ago
Bengaluru, Karnataka, India Icon plc Full timeStudy Start Up Associate II - India, 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 At ICON, it’s our people that set us apart. Our...
-
Centralized Study Associate I
2 days ago
Bengaluru, India Labcorp Full timeTo complete 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...
-
Study Start Up Associate Ii
5 days ago
Bengaluru, India ICON Full timeAt 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 and set us apart as an organisation: Accountability & Delivery,...
-
Centralized Study Associate I
7 months ago
Bengaluru, India Fortrea 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. Maintain project and technical documentation in an appropriate manner. Perform checks to ensure quality of work completed. Ensure timely...
-
Centralized Study Associate I
13 hours 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. Maintain project and technical documentation in an appropriate manner. Perform checks to ensure quality of work completed Ensure timely escalation as...
-
Centralized Study Spec I
13 hours 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...