Principal Clinical Database Designer

IQVIA; Bengaluru; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

IQVIA in Bengaluru, India is seeking a Senior Principal Clinical DB Designer to lead a team of database design professionals across multiple studies. You will act as a client contact for data management design, ensuring on-time delivery, quality, and alignment with project scope.

Responsibilities include providing expert review of CRF/e-CRF, database design and setup, validation programming, and Data Management Plans; mentoring staff; guiding proposals and scope of work; and participating in

Qualifications

• Bachelor's degree in Science/CS/IT or Bachelor in Technology.
• 10+ years of core Technical designer experience.
• Senior level experience in clinical data management and design.

Responsibilities

• Oversee a team of clinical database design professionals for delivery across multiple studies.
• Provide expert review and guidance for Data Management deliverables including CRF/e-CRF, database design and setup, validation definition and programming, and Data Management Plans.
• Define and prioritize resource requirements and manage resource assignments across projects.
• Attend customer meetings and lead discussions of project programming requirements and strategic planning.
• Mentor staff to develop Data Management programming processes and drug development expertise.

Skills

Leadership

Mentoring

Data Management

Communication

Project Management

Education

Bachelor's Degree in Science/Computer Science/Information Technology or Bachelor in Technology

Tools

CRF/e-CRF

Job description

Principal Clinical DB Designer Job Overview Oversee a team of clinical database design professionals for delivery and build of multiple studies in various platforms. May act as a client contact from clinical database designing team & responsible for project financials, new scope of work, relationship development. May also act as a SME for IT team for s/w application maintenance & adoption.

Essential Functions

• Global SME role.
• May act as a global librarian. Supports and performs CAPA, escalations and issues identified.
• Performs project financials check & review.
• Define and prioritize resource requirements and manage resource assignments across projects.
• Implement department/office objectives.
• Peer review of task at portfolio level.
• 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.
• Participate in the development and implementation of new processes and technology.
• 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 programming process, system, and drug development expertise.
• Provide design & programming input into proposals and scope of work.
• May participate in proposal defenses.
• Attend customer meetings and lead discussions of project programming requirements and strategic planning.
• Understand scope of work, budget, and scope assumptions. Identify out of scope work and provide revised costs with supporting documentation.
• Ensure project milestones are met according to agreed upon timelines. Actively manage quality throughout project.
• Responsibilities include planning, assigning, and directing work.

Qualifications

• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req
• 10+ years of relevant core Technical designer experience, 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 https://jobs.iqvia.com 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.

Experience Level Senior Level