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Study Start Up Manager (UK/EU Home based) - IQVIA Biotech

Employer
IQVIA Biotech
Location
Home based
Salary
On Application
Start date
16 Feb 2019
Closing date
20 Feb 2019

View more

Discipline
Clinical Research, Study Start Up
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

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.

 

Required skills

 

·        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

 

This role is full time, permanent and home based in the UK /EU.

 

 

 

 

 

 

 

Company

IQVIA Biotech is the global, enterprise-wide solution that provides flexible, tailored, integrated clinical and commercial solutions to small biotech and pharmaceutical companies, from planning through trial design and implementation to launch and commercialization.

We recognize that the needs of small companies are different than large companies, so we developed a separate business unit within IQVIA which provides a high-touch solution with high levels of service and hands-on attention, with the benefits of IQVIA’s data and expertise – including powerful analytics, resources, therapeutic experts and global footprint.

IQVIA Biotech has five therapeutic divisions. Complementing our successful history in Oncology, we have dedicated delivery teams in General Medicine – which includes Dermatology, Cardiovascular/Renal/Metabolics, Central Nervous System and Immunology.

Interested in being a part of this exciting and dynamic team?

Contact us today to find out more!

 

Company info
Website
Telephone
+44(0)1438 221122
Location
Ground Floor
Abel Smith House
Gunnells Wood Road
Stevenage
Herts
SG1 2ST
United Kingdom

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