Supervise and manage an assigned team of project delivery associates (including senior individual contributor roles) who manage or support studies to ensure quality, time and budget deliverables are met.
Work with staff to ensure that all project deliverables are completed ensuring quality deliverables on time and in accordance with Standard Operating Procedures (SOP), policies and practices.
Ensure that employees are trained, and individual development is aligned and in place to meet project and organizational needs.
Oversee assigned project(s).
Lead and manage the assigned work streams.
Line manage a team of Centralized Monitoring Leads and Centralized Monitors.
Lead overall customer delivery for small portfolios at an alliance level and work closely with CMS leads across studies to ensure that CMS deliverables are aligned with the customer KPIs and IQVIA SOPs.
Provide support at customer level for Risk Based Monitoring studies during set up phase for small studies.
Participate in the selection and on boarding process for new staff by conducting candidate review and participating in the interviewing process for support staff and lead roles.
Under supervision help with meeting department financial objectives by estimating requirements; preparing an annual budget; scheduling expenditures; analyzing variances.; initiating corrective actions.
Responsible for Overall Timelines, Quality and Productivity of the Projects, monitor KPIs regularly and meet SLA of the projects.
Present and discuss significant findings and risk mitigation plan at each Quarterly FMT Meeting.
Overall manage performance and Perform quality reviews and compliance checks for the central monitors assigned staff on the parameters outlined in Quality Management Plan.
Participate in Portfolio level initiatives.
Actively participate in client meetings.
Bachelor’s degree, or educational equivalence, in clinical, life sciences or pharma stream
Requires a minimum of 5 years of prior relevant experience.
Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonisation - Good Clinical Practice (ICH GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.
Good Clinical system expertise.
Strong written and verbal communication skills including good command of English language.
Results and detail-oriented approach to work delivery and output.
Understanding of clinical/medical data.
Excellent motivational, influencing and coaching skills.
Ability to work on multiple projects and manage competing priorities.
In depth therapeutic and protocol knowledge.
Strong organizational and problem-solving skills.
Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
Effective presentation skills.
Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.
Ability to lead team and effectively work in team.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. 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. Learn more at https://jobs.iqvia.com
