Centralized Study Spec Ii

2 days ago

Bengaluru, India Labcorp Full time

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. Execute high quality, timely monitoring and reporting plan(s) including specialized monitoring requests for approved protocols Support implementation of new monitoring tools Ability to work on Multiple studies and prioritize depending on conflicts Track and report metrics as determined by management according to required timelines. Proactively identify opportunities for process improvements and lead the implementation of process improvement activities to enhance deliverables. Support the implementation of tools internally to enhance deliverables Able to mentor and train others Work with Global Stakeholders 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. Support study team for contracts and budgets activities for investigative sites including but not limited to Investigatory Payment, Pass through payment processing & tracking 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
- Manage study documents and support eTMF management
- Support study teams to resolve data management queries
- Maintain study databases (CTMS, IWRS, EDC etc.)
- Track and follow up with CRAs for outstanding issues
- Support in generating the study specific reports.
- Manage internal/external communications
- Assist in ensuring training compliance for study teams
- Manage study payments (Site and Vendor) - Ex: Payment reconciliation and release
- Review study performance dashboard

**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 Spec I

    2 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As 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 time

    As 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 time

    As 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 Associate Ii

    1 week ago

    Bengaluru, India Labcorp Full time

    Centralized 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 Spec I

    5 days ago

    Bengaluru, India Labcorp Full time

    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...

  • Centralized Study Spec I

    2 days ago

    Bengaluru, India Labcorp Full time

    Support 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 - Review Electronic Data Capture updates and determine when certain budget items are payable - Assist in setting...

  • Centralized Study Spec I

    5 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As 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 Asso Ii

    1 week ago

    Bengaluru, India Labcorp Full time

    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...

  • Centralized Study Asso Ii

    5 days ago

    Bengaluru, India Labcorp Full time

    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...

  • Centralized Study Assoc Ii

    1 week ago

    Bengaluru, India Labcorp Full time

    Support 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 time

    Support 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 time

    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...

  • Centralized Study Associate Ii

    7 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As 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

    7 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As 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...

  • Central Monitor

    17 hours ago

    Bengaluru, India ICON Full time

    ICON is looking for a Central Monitor to be based in Chennai. The Central Monitor is responsible for listing review and central data analysis to support quality and risk reviews of projects, by highlighting/escalating trends. Job Responsibilities As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement...

  • Study Start Up Associate Ii

    1 month ago

    Bengaluru, Karnataka, India ICON Plc Full time

    Study 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

    5 months ago

    Bengaluru, Karnataka, India Icon plc Full time

    Study 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

    6 days ago

    Bengaluru, India Labcorp Full time

    To 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

    1 week ago

    Bengaluru, India ICON 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,...