Centralized Study Associate Ii

3 days 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 the study specific reports
- Follow up with CRA for resolution of the outstanding issues/action items related to assigned tasks.
- Assist the Lead for any study specific data review related tasks.
- To follow all applicable departmental Standard Operating Procedures and Work Instructions.
- To complete required trainings according to required timelines.
- To complete day-to-day tasks ensuring quality and productivity.
- To manage project and technical documentation in an appropriate manner.
- To provide administrative and technical support to internal departments and teams as needed.
- To perform checks to ensure quality of work completed.
- To ensure timely escalation and issue resolution as needed.
- To track and report metrics as determined by management according to required timelines.
- To assist with the implementation of revised processes and procedures.
- To 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.
- To assist in the preparation of new investigator submission packages for site/regulatory submission.
- To assist in Investigator Payment Processing
- To assist the study, startup teams with tasks required for site start up activities.
- To manage and support assigned studies for upload as per set objectives
- To follow up with study team on uploading queries

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

  • Study Start Up Associate Ii

    4 weeks 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...

  • 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 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

    6 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...

  • Study Start Up Associate Ii

    4 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...

  • 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

    3 days 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,...

  • Study Start Up Associate Ii

    4 weeks 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 What ICON can offer you: - Our success depends on the quality of...

  • Centralized Study Asso 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...

  • Centralized Study Assoc Ii

    3 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 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...

  • 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,...

  • Research Associate II Specialist

    4 weeks ago

    Bengaluru, Karnataka, India Lifelancer Full time

    About the RoleWe are seeking a highly skilled Research Associate II to join our team. This role is ideal for someone with experience in clinical research and a strong understanding of industry regulations.Job DescriptionThe Research Associate II will be responsible for designing and developing calendars, budgets, and case report forms for clinical trial...

  • Study Start Up Associate I

    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,...

  • Centralized Study Associate I

    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. Maintain project and technical documentation in an appropriate manner. Perform checks to ensure quality of work completed. Ensure timely...

  • Centralized Study Associate I

    2 days ago

    Bengaluru, India Labcorp Full time

    Position provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). ¨ Maintains an understanding of applicable regulatory requirements. ¨ Managing electronic Trial Master Files (eTMF), (Trial, Country and Site artifacts) for clinical studies in...

  • Study Delivery Associate

    4 months ago

    Bengaluru, Karnataka, India GSK Full time

    **Site Name**: Bengaluru Luxor North Tower **Posted Date**: Sep 9 2024 **VEO Study Delivery Operations** Value Evidence and Outcomes (VEO) delivers evidence that demonstrates the safety and value of our medicines. VEO is an essential contributor to medicines development and commercialization. VEO builds a deep understanding of patient populations, patient,...

  • Clinical Research Associate II Specialist

    1 month ago

    Bengaluru, Karnataka, India Lifelancer Full time

    About the RoleAre you passionate about making a difference in the world of clinical research and advancing human health? We are seeking a highly motivated and organized Clinical Research Associate II Specialist to join our team at Advarra.Job SummaryThis is an exciting opportunity to work with a dynamic team that is dedicated to fostering an inclusive and...