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Senior Director, Clinical Project Lead (CPL) - Early Development

Brentford

Job Type

Job Function

Medical and Clinical

Location

Brentford

On-Site or Remote

Job Type

Salary

Competitive salary and benefits

About the Role

*Job description* *Site Name:* USA - Maryland - Rockville, Belgium-Wavre, Cambridge Park Drive, GSK House, Italy - Siena *Posted Date:* Jan 18 2024 *Senior Director, Clinical Project Lead (CPL) – Early Discovery* *POSITION SUMMARY* The *Senior Director, Clinical Project Lead (CPL), Early Development* focuses mostly on early phases of development and is also involved in the early conception of long-term Phase I to IV Clinical Development activities within a group of early discovery programs and task forces within the Discovery Product Unit. The CPL, Early Development is accountable for the development, execution, and oversight of Phase I or I/II clinical studies, including the integration of global considerations into strategic decisions. The CPL, Early Development works with a cross functional team to create high level development plans for early assets in the vaccines pipeline. *KEY RESPONSIBILITIES IN DETAIL* - Manages the team of Clinical Science Leads (CSLs) and Senior Clinical Science Leads (SCSLs), assigned to the development program, who lead the clinical matrix teams responsible for clinical study activities, including study design, protocol development, input into statistical analysis plans, medical data cleaning and reconciliation, data analysis and interpretation, in compliance with Good Clinical Practice (GCP) and GSK policies and procedures. - Accountable for the study design and serves as the Clinical Sponsor Signatory for the protocol. - Accountable for the final analysis and interpretation of clinical trial data and serves as the Clinical Sponsor Signatory for the clinical study report. - Serves as the primary point of contact for clinical with the Principal Investigators (PIs). - Accountable for the authorship and approval of clinical documents for regulatory submissions, including Clinical Expert Statements, and serves as the Program Clinical Expert for input into regulatory documents/meetings. - Accountable to ensure disclosure and publication of clinical trial data according to ICJME and relevant GSK policies and guidelines. - Supports cross-functional partners as necessary for activities including External Expert (EE) engagement and PI selection. Supports the regional Medical Affairs teams as needed. - Drives the end-to-end integrated clinical development strategy that is appropriately resourced to achieve regulatory approvals, reimbursable/recommended vaccines, and successful life cycle management. Accountable for consistently achieving project timelines in global programs with high quality of execution. Participates in key budget/forecast activities in collaboration with Vx Clinical Science Excellence Lead, and Clinical Operations Asset Lead to ensure milestones realisation and resource optimisation. - Champions implementation of innovative methods and processes within clinical plans, encourages others to think differently and come up with business solutions. - Establishes expeditious clinical development timelines, incorporating key decision points and Go/No Go criteria in CDP. - Strategic Leadership: Integrates scientific rationale, regulatory requirements, product development plan and commercial goals to optimise clinical study designs aligned with the IEP and CDP. - Represents the Clinical Science function at the Vaccine Development Team (VDT), Vaccine Commercialisation Team (VCT), and Discovery Project Team (DPT), as applicable. Supports the VDT/VCT/DPT as necessary through provision of thoughtful senior clinical input and technical expertise to global development questions, including contributions to internal and external briefing documents and presentation materials. Serves the primary clinical voice for the project at governing bodies such as Development Review Board (DRB) Research Review Board (RRB) and technical committees such as Global Safety Board (GSB), Protocol Review Board (PRB) and Toxicology Working Group (TWG). - Collaborates with cross-functional partners in Preclinical, Technical Development, Global Clinical Operations, Biostatistics, Regulatory Affairs, Medical Affairs, Commercial, Value Evidence and Outcomes, Safety, etc. to ensure effective delivery of the project according to agreed plans. - If requested, involved in the development and execution of external collaborations. May be requested to support business development activities, including the performance of due diligence reviews. - Plays an active role in the technical and leadership development of Clinical Sciences staff and maintains oversight and strategic intent of the program. Ensures effective coaching and mentorship of more junior members of the clinical team. - Core member of the Vaccines Clinical Science Cluster Leadership Team. *CANDIDATE PROFILE – QUALIFICATIONS AND EXPERTISE* *Basic Qualifications* - MD with experience conducting clinical research independently. - Industry experience in vaccine clinical research, or related field (e.g., infectious diseases, immunology). - Experience in clinical research, translational science, and biomedical research regulation, including ICH and GCP. - Experience in conducting Phase I/II clinical development. - Experience managing complex programmes. - Fluent knowledge of spoken and written English. *Preferred Qualifications* - PhD in a relevant field. - MD/PhD specialising in the field of paediatrics, obstetrics and gynaecology, infectious diseases, clinical epidemiology, or pharmacoepidemiology. Previous experience in clinical vaccinology preferred. - Experience in conducting Phase III clinical development. - Knowledge and understanding of causes of infectious diseases, health interventions and the global public health landscape. - Sensitivity to the needs of a diversified ethnic groups and ability to build rapport across the spectrum. - Excellent people and team management skills. - Strategic thinking skills and achievement oriented. - Able to critically analyse information, identify strengths and weaknesses of approaches and develop remedial actions to mitigate risks. - Ability to understand high level corporate and business objectives: rapid, flexible, innovative working and decision making. - Executive capability with strategic planning and budget processes such as analytical thinking. - Strong leadership, coalition-building, and communication skills. - License to practice medicine and board and/or professional certification is an asset. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. *Why Us?* 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 organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030. 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 workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. *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. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.

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