Senior Clinical Data Manager

BeiGene

3d•$108,700 - $143,700

About The Position

The Senior Clinical Data Manager's role is responsible for assigning and/or driving all aspects of the clinical trial data management activities, from study start up through database lock, and is responsible for the quality of all data reviewers’ deliverables. BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

Requirements

Proficient computer skills, including Microsoft Office applications
Working knowledge of at least one EDC system, Medidata Rave is preferred
5+ 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 for ICH and regulatory environment as it pertains to data management and good understanding of data management and phases of clinical trials
Have a good understanding of data management knowledge and understands the phases of clinical trials
Strong communications skills and capable of solving issues independently.
Strong project management skills
Excellent written, verbal and organizational skills
Good interpersonal skills and have the capability to lead studies DR(s) and prioritize DM activities.
Must be detail-oriented
Travel may be required as per business need, ability to travel domestically and internationally.

Nice To Haves

Medidata Rave is preferred
Oncology experience preferred

Responsibilities

Supports and works closely with study lead data manager(s) for assigned clinical studies.
Performs data cleaning/reconciliation activities as specified in company procedural documents and study-specific Data Management (DM) documents.
Manages queries on assigned clinical studies.
Generates and delivers reports to study team members.
Supports external data reconciliation, in addition to serious adverse event reconciliation.
Ensures laboratory data, if applicable, and associated lab normal ranges are reviewed and reconciled.
Supports the creation and maintenance of DM documentation (e.g., Data Management Plans, eCRF Completion Guidelines).
Helps to ensure DM documents are filed per company Standard Operating Procedures (SOP) and Work Instructions (WI).
Supports eCRF and edit check specifications development as necessary to support data collection and analyses required by the protocol.
May work closely with database builders during clinical database build and programming of eCRF, edit checks, and reports.
Participates in User Acceptance Testing (UAT) activities for clinical database build and modifications.
Participates in UAT activities for data transfers and programmed report outputs.
Assists with Site and User management in clinical database of assigned clinical studies.
May lead one or more Phase I to Phase II studies under supervision of manager.
Will have the opportunity to drive all data review related activities. This will also include identifying and escalating potential data issues to the Data Management Team when issues arise.
May work with vendors such as central laboratories in support of timelines and data-related deliverables.
May help identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from other project team members. This also includes mentoring other study team members when opportunities arise.
May help train other personnel on eCRFs and EDC.
May help support development and maintenance of SOP and WI related to data management activities.
Other duties as assigned.