RAVE Data Manager

Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Interactive, Technology and Operations services—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 514,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities. Visit us at www.accenture.com.

The RAVE Data Manager ensures the completeness and validity of the data in the clinical database.
Key Responsibilities:
- Ensure completeness and validity of the clinical trial data that has gone through data entry with good quality
- Study design and build, understand forms, visits, and data items collected.
- Perform data review, external data reconciliations, IVRS/external data integration.
- Review and resolve/action discrepancies identified by the system or through manual checks as per guidelines
- Create, Process and Action Data Clarification Forms as and when required
- Issue clarification/follow-up until closure per the Issue Escalation Tracker process/guidelines.
- Ensure timelines set by the client in terms of discrepancies resolved and clean patient delivery are met.
- Run RAVE reports for RAVE studies to clean clinical data.
- Perform UAT of edit checks, creation of edit check specifications and reports specifications.
- Perform form freezing/locking and understand overall database lock process.
- Perform discrepancy review and perform Self-Evident Corrections per DRP
- Perform SMT override, as and when required/requested.
- Perform discrepancy management for SAE, PV and Medical Monitor related discrepancies
- Perform SAE Reconciliation based on the frequency required
- Co-ordinate with sites for site data entry and site closures.
- Share study status with PDMs as when requested
- Perform query management.
- Perform Adhoc work or additional tasks as and when requested by clients.

Basic Qualifications:
- Minimum of 4 years of clinical data management experience (such as RAVE)
- Bachelor’s Degree
Preferred Qualifications:
- Excellent project planning and management skills.
- Knowledge of clinical drug development
- Knowledge of Rave database
- Basic Excel, Word & PC skills

Professional Skill Qualifications:
- High degree of accuracy and attention to detail
- Ability to manage timelines
- Good communication skills (Verbal/Written)
- Analytical approach
- Problem solving