Sr Clinical Data Prgrming Lead
Talent Acquisition Business Partner
- Full Service Division
About the role
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- Serves as the clinical data delivery lead on multiple study specific programming setup, leading clinical data programming activities on multiple studies of simple to moderately complex design, with competent clinical data delivery experience and knowledge.
- Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
- Reviews specification documents created by study teams, such as data transformation specifications and programming specifications.
- Co-ordinates and manages study database updates and out of scope impacts as specified per change Request documents and procedures. Performs an Impact Analysis and Risk Assessment of the proposed changes.
- Serves on project teams to coordinate and lead development activities for multiple clinical data programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive criticism. Keeps those responsible for project management informed of any issues that might impact project target dates, scope or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.
- Trouble-shoots and solves study data delivery issues and/or external data integration issues and/or change request issues using the appropriate applications.
- Plan for the study clinical data delivery in detail thereby providing clarity on all aspects of the setup progress.
- Ensures high quality deliverables by providing senior review of study level/program-level/multi-study core deliveries for accuracy.
- Attends sponsor audits and assists with in-progress audits, including presenting the Clinical Data Delivery process and procedures and pretending the validation documentation produced by the Clinical Data Services Group.
- Ensures programming processes are compliant with applicable SOPs.
- Ability to run existing programs to produce internal and Sponsor deliverables
- Provide ongoing support, mentorship and training as appropriate, to members of the CDMS or CDS team involved
- Bachelor’s degree in information systems, science or related discipline.
- Minimum 2 years experience building study databases or 4 years experience in clinical data programming
- SAS Programming experience required
- Proficiency in CDISC
- Trained in Data Standardizing
- Proficiency in Business computer skills
- Documentation skills
- Thorough knowledge of ICH Guidelines and GCP including regional regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing
- Excellent oral and written communication and presentation skills.
- In depth knowledge of clinical trial process and data management, clinical operations, and systems applications to support operations.
- Demonstrated organizational skills to handle multiple competing priorities simultaneously across an assortment of projects and initiatives.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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