Project Data Manager

BeiGene

7d•$123,200 - $163,200

About The Position

The Project Data Management role is responsible for all aspects of the clinical trial data management process from study start up through database lock and support of clinical study report (CSR) activities for assigned studies. This role is also accountable for quality of deliverables and resource efficiency of assigned studies. This role may be expected to lead multiple clinical studies and/or oversee CRO/FSP vendors for multiple clinical studies.

Requirements

Proficient computer skills, including Microsoft Office applications
Working knowledge of at least one EDC system, Medidata Rave is preferred
6+ years of experience in clinical data management in the pharmaceutical/biotechnology industry
Oncology experience preferred
Ability to work in cross-functional team-oriented environments
Understanding of ICH and regulatory environment as it pertains to data management
Experience with SDTM/CDASH
Strong project management skills
Excellent written, verbal and organizational skills
Must be detail-oriented
Bachelor’s degree or equivalent in a health-related field preferred

Nice To Haves

Medidata Rave is preferred
Oncology experience preferred

Responsibilities

Lead studies within a program
Oversee data managers working on studies either in-house or CRO/FSP resources
Serves as active member of Clinical Study Teams.
Collaborates with other functions to develop timelines and ensure that clinical data management deadlines are met.
Defines external data transfer specifications and works with external vendors in support of timelines and data related deliverables.
Ensures process is in place to review and reconcile lab data with lab normal ranges
Develops or oversees development of eCRF and edit check specifications as necessary to support data collection and analyses required by the protocol.
Works closely with database builders during programming of EDC databases, edit checks and reports.
Drives and performs User Acceptance Testing (UAT) activities for clinical trial database build and modifications.
Develops or oversees development of study-specific eCRF Completion Guidelines and Data Management Plans
Creates and maintains data management documentation.
Ensure data cleaning activities as specified in the Data Validation Specifications and Data Management Plan.
Works with coding group to ensure coding is applied to assigned clinical studies in conjunction with study timelines and deliverables.
Defines listings in support of data management, clinical and medical review of data.
Identifies and troubleshoots operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from other project team members.
Will have the opportunity to drive all data review related activities. This will also include identifying and escalating potential data issues to LDM when issues arise.
Trains other personnel on eCRFs and EDC, as needed.
Ensures coordination with Pharmacovigilance on serious adverse event reconciliation.
Reviews and provides feedback on draft protocols, Statistical Analysis Plans, CSRs and other documents as required.
Support management team with continued process improvement/innovation for the department and participates in the development and maintenance of Standard Operating Procedures (SOPs) and Work Instructions related to data management activities.
Will oversees data managers working on studies either in-house or CRO/FSP resources to ensure studying the support on the studies are sufficient.
Collaborates with program lead and other functions to ensure program-consistent, high-quality and on-time data delivery.
May mentor other junior Clinical Data Managers.
Other duties as assigned.