Clinical Laboratory Study Manager

Site Name: Canada - Ontario - Mississauga Posted Date: Nov 29 2024 One Development – Human Biological Samples Management Central Team (HBSMCT) support Medicines Clinical trials involving Human Biological Samples (HBS) that are collected, stored, transferred, analysed, and destroyed as part of the clinical trial. The management of the HBS and associated laboratory activities need to be coordinated in a manner that ensures compliance (ethical, legal, and regulatory) and quality to appropriate standards. The Laboratory Study Manager within HBSM-CT is responsible for the operational setup & follow-up of central laboratory related activities for a project or a group of studies to guarantee alignment among the entire network and with Clinical Operations to support delivery of laboratory results timely at right quality and cost. The laboratory network is made from:

• Central laboratories (CL) in charge of global laboratory support to clinical studies such as sampling material delivery, sample management, support to testing oversight.
• GSK Laboratories in charge of development, validation, and sample analysis. o Third Party Laboratories in charge of development, validation, and sample analysis
• Vendors/Laboratories responsible for long-term storage of untested HBS (for future research).

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Key responsibilities For a project or a group of studies, lead activities related to HBSM and ensure effective interface between Clinical laboratories and GSK Clinical Study Team including members such as: Study Delivery Lead (SDL),CPEM, Oncology-EMU IVIVT, Human Genetics. Provide input in clinical study protocol development (clinical laboratory part) including laboratories set up and instructions for investigators sites. Be main point of contact for the clinical study team regarding clinical laboratories, a well as responsible for overview of HBSM in the assigned projects including support for investigator sites (mainly based on the cooperation with the Local Delivery Leads – LDLs) and testing issues in CL Be the HBS custodian for the study, from study start to study end according to the GSK HBSM SOP and related written standards. For each study, define the operational set-up to align HBS flows, testing activities and data flows (in cooperation with GSK Data Management) and assure it is in line with the other stakeholder’s constraints. Own the BFL (Biospecimen Flow & Logistics Form) and Samples Risk Assessment process and documents. Ensure that all study related activities are operationally set-up and conducted in line with the approach agreed with the clinical study team. Oversight of chain of custody of HBS throughout the lifecycle of the study, including site - central lab and provide consultations for HBSM CT in case of HBSM by Third Party Laboratories. Act as Central Laboratory Subject Matter Expert (SME) for one or several processes of the team. Ensure standard processes and ways of working are in place across all project and studies for all key activities of LSMs, e.g., HBS custodian, study set-up with central laboratory, BFL process, blinding & reconciliation strategy, etc. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals,

• 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.
• +5 years operational experience in clinical laboratory activities and clinical study conduct
• +3 years proven experience in clinical project planning, project management and issues resolution

Preferred Qualifications : If you have the following characteristics, it would be a plus,

• 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 and FDA or other competent authority inspection exposure
• Experience of budget management
• Experience in direct & indirect people management is an asset.

#LI-HYBRID Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. GSK is an equal opportunity employer committed to diversity and inclusion.  We welcome applications from all qualified individuals to apply to our career opportunities. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at canada-recruitment@gsk.com .  Please do not send resumes to this e-mail and instead apply through the online application process of this posting. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.