Global Data Management

Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF database design and set-up validation definition and programming Data Management Plan and database deliverables to internal and external customers. Provide technical advice and solutions with internal and external customers to solve problems and improve efficiency. Ensure that staff is trained and compliant with current operating procedures and work instructions and project scope of work. Identify and address professional development/training needs of staff. Mentor staff members to develop Data Management process system and drug development expertise. Provide operational input into proposals and scope of work. Participate in proposal defenses. Hold at least bi-monthly meetings with direct reports to discuss at a minimum: project status including timelines delivery updates financial aspects of the group or project and potential risks associated mitigation and support required; status of any initiatives that they may be involved in; the teams utilization rates; the direct reports training and other administrative obligations such as Standard Operating Procedures (SOPs) and corporate training mandates; personnel issues; and career or training objectives. Develop and implement plans for measuring and improving employee engagement ensuring global consistency.
Collaborate with project leads to address work scheduling for current and projected projects staffing needs technological needs and projected peak workloads ensuring global consistency where possible. Develop and manage associated action plans to hold members accountable. Efficiently conveying messages from leadership to direct reports and teams as well as effectively communicating issues and opportunities up to leadership. Might be needed to serve as the designated substitute or alternatively ensure coverage is in place for direct reports during their absence or in case of turnover. Attend and participate in Bid Defenses Kick off Meetings (KOM) as applicable. Support Request for Information (RFI) Request for Pricing (RFP) and budgets as requested. Participate / Support internal and external audits and inspections as required. Also ensure required staff is assigned trained and prepared to support.

Technical Skills:
Experience on clinical data management.
Experience working on TA like Oncology.
Extensively work on rave EDC tool.

Educational Qualification:
Bachelors Degree Clinical biological or mathematical sciences or related field Req Equivalent combination of education training and experience in lieu of degree.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.

Employment Type : Full-Time
Experience: years
Vacancy: 1