Job Title: Global Study Management Associate Director Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.
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Our approach to R&D Position Summary Join GSK as a Global Study Management Associate Director and play a pivotal role in advancing clinical research on a global scale. In this role, you will lead and oversee the planning, execution, and delivery of clinical studies, ensuring high-quality data and operational excellence. You'll collaborate with cross-functional teams, drive innovation, and contribute to GSK's mission of uniting science, technology, and talent to get ahead of disease together. This is an opportunity to make a meaningful impact while growing your career in a supportive and inclusive environment. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Lead the planning and delivery of global clinical studies, ensuring timelines, budgets, and quality standards are met. - Collaborate with cross-functional teams to optimize study design, feasibility, and operational strategies. - Oversee risk management and mitigation strategies to ensure successful study execution. - Drive continuous improvement in study management processes, leveraging data and insights to enhance efficiency. - Build strong relationships with internal and external stakeholders, fostering collaboration and alignment. - Ensure compliance with regulatory requirements, Good Clinical Practices (GCP), and GSK's quality standards. Basic Qualifications We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Bachelor's degree in a relevant field such as life sciences, clinical research, or healthcare. - Minimum of 5 years of experience in clinical study management or clinical operations. - Strong knowledge of Good Clinical Practices (GCP) and International Council for Harmonization (ICH) guidelines. - Proven ability to manage complex projects and lead cross-functional teams. - Excellent communication and interpersonal skills, with the ability to build relationships across diverse teams. - Experience working in a global environment and managing studies across multiple geographies. Preferred Qualifications If you have the following characteristics, it would be a plus: - Master's degree in a science-related field or advanced degree in clinical research. - Experience in managing large-scale, global clinical trials across multiple therapeutic areas. - Strong analytical skills and ability to use data to inform decision-making and improve processes. - Knowledge of emerging trends and technologies in clinical research and study management. - Experience with risk management and quality improvement initiatives in clinical operations. - Ability to adapt to a fast-paced environment and manage multiple priorities effectively. This position is hybrid, requiring a minimum of two days per week at our Mississauga office. Ready to make a difference? Apply today and join us in our mission to get ahead of disease together!
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