Clinical Development Associate Director
1 month ago
We are seeking an experienced Clinical Development Associate Director to join our team at GSK. As a key member of our Global Clinical Development organization, you will be responsible for leading the design, execution, and reporting of clinical trials, as well as providing leadership in project teams and across matrix teams.
Key Responsibilities- Plan and lead the delivery of oncology studies to time, quality, budget, and company standards.
- Drive assessment, selection, engagement, management, and oversight of appropriate vendors.
- Make decisions that balance risk and benefit, taking action to mitigate risk where appropriate.
- Work with matrix partners, asset lead, and/or manager to develop and manage study-level budget within project allocation.
- Prepare materials for governance and/or financial review cycles and provide expert clinical operational input into protocol development.
- Lead risk management and quality efforts to ensure study compliance and continual inspection readiness.
- Partner with Data Management and Clinical Sciences to develop the data cleaning strategy for the study and collaborate with Oncology-aligned staff in global functions to deliver the Clinical Study Report.
- Work with the Oncology patient councils to develop patient-centric documents and address patient burden.
- Bachelor's degree in life sciences or related discipline.
- Extensive clinical development experience equivalent to 6 years as a global study leader, with proven experience in driving operational study delivery to time, cost, and quality within the pharmaceutical industry or CRO environment.
- Proven operational experience leading global oncology clinical trials and knowledge of essential global regulatory guidelines and ICH/GCP.
- Proactively identify and resolve issues to ensure timely study delivery to quality, timelines, and budget.
- Demonstrated experience leading in the matrix environment to deliver projects, develop clinical plans, and manage change.
- Oncology phase III global registrational study leadership experience.
- Proven clinical development experience across all phases of development (I-IV).
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.
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).
We believe in an agile working culture for all our roles and are committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease.
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Clinical Development Associate Director
1 month ago
Stevenage, Hertfordshire, United Kingdom GSK Full timeJob Title: Clinical Development Associate DirectorWe are seeking an experienced Clinical Development Associate Director to join our team at GSK. As a key member of our Global Clinical Development organization, you will be responsible for leading the delivery of oncology studies to time, quality, budget, and company standards.Key Responsibilities:Lead the...
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Clinical Development Associate Director
1 month ago
Stevenage, Hertfordshire, United Kingdom GSK Full timeJob Title: Clinical Development Associate DirectorWe are seeking an experienced Clinical Development Associate Director to join our team at GSK. As a key member of our Global Clinical Development organization, you will be responsible for leading the delivery of oncology studies to time, quality, budget, and company standards.Key Responsibilities:Lead the...
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