Global Study Asset Manager

Talentmark Limited; Welwyn Garden City; Hybrid; GBP 467,000 - 519,000; Full time

Job summary

Talentmark Limited is recruiting for a Global Studies Asset Manager on a 6-month contract. The role is hybrid, with 2/3 days on site and the remainder from home, in Welwyn Garden City, UK.

The role involves coordinating study management across a group of studies, driving clinical ops innovation, and building strong partnerships with CROs to maximize expertise. KPIs will be developed and tracked using company systems.

Qualifications

• Hold a relevant degree or equivalent experience.
• Extensive operations experience in life sciences.
• Exposure to study management from concept to database lock.
• Experience in phase 3 in a requirement.

Responsibilities

• Coordinate and deliver study management across a group of studies within an asset's portfolio.
• Drive innovation in clinical operations by contributing to new approaches.
• Build and role model effective study partnership behaviours with your TA aligned CRO partner to maximise expertise.
• Develop and oversee KPIs for areas of responsibility using company tracking systems.
• Lead 3rd party vendor selection, vendor identification, setup, oversight and close out to ensure delivery.

Skills

Life sciences operations

Study management

KPI development

Vendor management

Education

Relevant degree

Job description

Talentmark are recruiting for a Global Studies Asset Managerto join a company in the pharmaceutical industry on a contract basis for 6 months.This role is hybrid, with 2/3 days on site and the rest working from home.

Company

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Salary

£339.27 - £376.97 PAYEor £450 - £500 UMB

Global Studies Asset Manager Role

• Co-ordinate and deliver the study management aspects of a group of studies within an asset's portfolio.
• Drive innovation in clinical operations by thinking of and contributing to the implementation of new approaches.
• Build and role model effective study partnership behaviors and mindsets with your TA aligned CRO partner to ensure we maximize expertise.
• Develop and oversee key performance indicators (KPIs, quality and operational) for areas of responsibility by using company tracking systems.
• Lead 3rd party vendor selection Vendor identification set up, and oversight and close out to ensure delivery to contract.

Your Background

• Hold a relevant degree or have equivalent working experience.
• Extensive and relevant operations experience in life sciences.
• Study management operational planning and execution exposure from concept through to database lock.
• Experience in phase 3 in a requirement.

Company

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

It is essential that applicants hold entitlement to work in the UK

Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check