• Study Start-Up Manager Jobs in Austria

  • Iqvia
  • Austria

Job Description:

Job Description IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward

IQVIA Biotech is expanding its Study Start Up group and is looking for Study Start Up Managers to be home based in the UK/EU

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 and Clinical Trial Managers in setting priorities for study start up This individual works with the VP of Operations to set forward looking strategy for the Department as it strives to meet its internal objectives to support overall IQVIA Biotech top and bottom line performance

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

Demonstrated knowledge of quality assurance related to study startup

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

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage It takes brave minds, pushing the boundaries to transform healthcare Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients

Forge a career with greater purpose, make an impact, and never stop learning

Job ID R1086394

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Consulting Services
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 18th Mar 2020

Key Skills:

Company Profile:


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