ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

The Clinical Study Manager (Biosampling) is responsible for the operational set-up & follow-up of central laboratory (CL) related activities for a project or a group of studies to guarantee alignment amongst the entire network and with Clinical Operations to support delivery of laboratory results timely at right quality and cost.

What You Will Do:

You will manage day-to-day clinical trial management activities, focused on the operational set-up & follow-up of central laboratory (CL) related activities for a project or a group of studies to guarantee alignment amongst the entire network and with Clinical Operations to support delivery of laboratory results timely at right quality and cost.

Key responsibilities include:

• (copy from Job Description)

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities. Excellent networking capabilities and ability to influence and manage stakeholders at all levels of the organization. The ability to facilitate and lead cross functional meetings/challenge status quo and inefficient ways of working and need to be comfortable in a mediation role.

Required qualifications:

·        Master’s degree in medical/life sciences or equivalent background.

·         Demonstrated expertise in Project Management beyond their own field of expertise.

·         Demonstrated capability to integrate complex inter-departmental links, processes, databases, and systems.

·         Demonstrated knowledge and competency in laboratory processes and extended knowledge of ICH-GCP/GCLP rules.

·         Demonstrated fluency in spoken and written English beyond scientific English.

·         Good holistic view especially to proactively detect problems and define possible solution and/or to surface issues to Management.

Job Related Experience (minimum requirements):

·         At least 5 years of operational experience in clinical laboratory activities and clinical study conduct

·         Proven experience in clinical project planning, project management and issues resolution

·         Ability to quickly integrate with GSK clinical development processes and global network to build strong partnership with lab vendors and GSK stakeholders.

·         Experience of managing business remote matrix network of internal and external stakeholders of multicultural and multidisciplinary people with different expertise and various scientific background

·         Ability to align all the parties involved to build alliances and influence across national and cultural boundaries (up to 20 in different countries, including Africa and China)

·         Experience in leading various operational meetings

·         FDA or other competent authority inspection exposure

·         Experience of budget management

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply