IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech is expanding its Study Start Up group and is looking for Study Start Up Managers to be home based throughout Europe or India .

The SSU Manager is responsible for providing customer-focused leadership in the execution of operational strategy and management of start-up activities for projects or programs. This includes the overall management and oversight of the following processes: site feasibility, regulatory approval, and site contracts.  They may be assigned to manage the site start-up activities for a country, region, or entire global trial.

The SSU Manager also has responsibility for maintaining internal tracking for study site status from initial site contact through site initiation. This position works directly with Director of Clinical Monitoring, VP Operations, Project Managers, Regulatory managers  and Clinical Trial Managers in setting priorities for study start up. 

• Demonstrated ability to manage a team of people around clinical research related activities.

• Demonstrated knowledge of quality assurance related to study start up.

• Demonstrated ability to form strong working relationships across functional boundaries.

• Demonstrated ability to motivate, lead, and grow a study start up team.

• Excellent written and verbal communication skills.

• Exceptional ability to conceptualize, develop and manage timelines.

• Ability to delegate.

• Ability to manage multiple projects and priorities.

• Ability to set baseline targets, track trends and implement mitigation plans.

• Demonstrated knowledge of resources required to permit protocol implementation.

• Considerable ability to develop and maintain productive relationships with coworkers, managers and clients.

• Ability and willingness to travel.

• Working knowledge of current clinical trial regulations.

• Fluency in Spoken and written English

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