Centralized Study Associate I
9 hours ago
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 accordance with TMF processes, working with key study personnel such as the Study Team Member
- ¨ Responsible for document classification under Smart Inbox (when applicable), ARC review, document deletion. TMF Classifiers or Start Up team members as part of the SSU Vault Model typically fulfill this role (TMF Classifier).
¨ Maintains the TMF in a state of audit readiness for quality and compliance by:
1. Visual quality checks of e-documents prior to release to confirm image clarity and readability.
2. Performing Audit Ready Checks on individual documents uploaded in the eTMF system for every study, ensuring context is accurate;
¨ Comply with metrics established for performance.
¨ Process and track final essential artifacts required throughout all phases of the study in accordance with Labcorp SOPs, sponsor SOPs, GCP and ICH guidelines.
¨ Manages the identification of operational issues and resolutions related to the TMF.
¨ Prepares the TMF for QA or Sponsor audits, the resolution with identifying and implementing corrective actions to findings in audit reports.
¨ Participates in Internal Audits & Client Audit as per study requirements.
¨ Collaborates with all members of BP&S.
¨ Ensures overall client satisfaction for all studies.
¨ Participates in business improvement initiatives to drive quality, productivity and continuous improvement of business processes.
¨ Maintains an understanding of applicable regulatory requirements.
¨ Attend internal or external study team meetings as required.
¨ Perform other related duties as assigned.
**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.
-
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...
-
Centralized Study Associate I
2 weeks 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...
-
Study Start Up Associate I
10 hours ago
Bengaluru, Karnataka, India ICON Plc Full timeSSUA I, Bangalore, Office based 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 I to join our...
-
Central Global Study Associate
4 days ago
Bengaluru, Karnataka, India AstraZeneca Full timeTypical Accountabilities: - Coordinate SD system activities and collection of SD metrics. Facilitate maintenance of study delivery system data and implementation of system enhancements. Develop reporting tools for SD Systems. Maintain an awareness of the external Process and Technology environment to identify opportunities for Study Delivery - Delivers...
-
42199 - Assoc Centralized Monitor
6 days ago
Bengaluru, India Novasyte Full timeJob Overview Provide project related assistance to assigned project teams. Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements. Meeting quality and timeline metrics. Essential Functions - Complete appropriate role-specific training to perform job duties.; -...
-
Centralized Study Asso I
2 weeks 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
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...
-
Central Global Study Associate
4 days ago
Bengaluru, Karnataka, India AstraZeneca Full time**Job ID** R-228789 **Date posted** 06/13/2025 Typical Accountabilities: - Coordinate SD system activities and collection of SD metrics. Facilitate maintenance of study delivery system data and implementation of system enhancements. Develop reporting tools for SD Systems. Maintain an awareness of the external Process and Technology environment to identify...
-
Centralized Monitoring Assistant
2 weeks ago
Bengaluru, India Novasyte Full timeJob Overview Provide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics.; Essential Functions - Complete appropriate role-specific training to perform job...
-
Reporting Associate I
9 hours ago
Bengaluru, India Labcorp Full timeThe statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. **Job Summary**: **Essential Job Duties**: - The Reporting Associate I learns and performs the duties of drafting and finalizing nonclinical study reports and completes the...