Associate Clinical Data Manager at IQVIA

Responsibilities

• Serve as Data Team Lead (DTL) on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory studies
• Provide leadership to CDM team.
• Manage CDM customer relationship for CDM project team to include leading (with minimal guidance) CDM customer negotiations on complex timeline, budgetary and other issues.
• Provide marketing capabilities presentations and business development presentations.
• Serve as Data Operations Coordinator (DOC) for one or three global clinical trials with fewer than 25 operations staff (excludes DE) or 20-40 central laboratory studies, or serve in a leadership role to a specific DM Task.
• Serve as back-up for Data Operations Coordinator or Data Team Lead
• Provide leadership to Operations team
• Provide technical expertise
• Serve as a Subject Matter Expert (SME)
• Provide leadership and expertise in a specific CDM task or technology
• Manage delivery of projects through full data management process life-cycle.
• Management of Project timelines, Quality issues, Resource management and SOW (scope of work) / budget.
• Provide justification for customer negotiations.
• May serve as Project Manager for single service data management projects.
• Manage comprehensive data management tasks pertaining to the documented project specifications.
• Manage comprehensive quality control procedures.
• Provide data management expertise and data management process improvement to CDM management.
• Mentor other team members in training and developing data management expertise.
• Independently bring project solutions to the CDM team and the CDM Department.
• Manage a focus team or a best practice team
• Manage the development and implementation of new technology/tool.
• Present at professional conferences and/or publish articles in professional journals.
• Provide CDM with technical expertise.
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
• Perform other duties as directed by the functional manager.
• Meet objectives as assigned.
• Develop and maintain good communications and working relationships with CDM and project teams.

Required Knowledge, Skills And Abilities

• Thorough knowledge of the data management process and experience in specialized data management skills (e.g., therapeutic, extensive knowledge, SAE reconciliation, central laboratory, and/or new technology
• Knowledge of operating procedures and work instructions and the ability to apply them in practice
• Excellent experience and organizational, communication, and demonstrated expert data management skills
• Comprehensive understanding of clinical drug development process (detail oriented)
• Ability to establish and maintain effective working relationships with co-workers, managers and clients

Minimum Required Education And Experience

• Bachelor’s degree, or educational equivalence, in clinical, biological or mathematical sciences, or related field, or nursing qualification with 5 years’ experience in clinical trials within a similar function, including proven competence in managing delivery of multiple projects simultaneously through full data management study life-cycle, including large trials >1000 patients; and including experience in handling customer negotiations (e.g. bid defence meetings); or equivalent combination of education, training and experience

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.