At a Glance
- Tasks: Lead cross-functional teams to deliver global clinical studies on time and within budget.
- Company: Join IQVIA, a top global provider of clinical research services and healthcare intelligence.
- Benefits: Enjoy opportunities for mentorship, innovative projects, and a dynamic work environment.
- Other info: This role is not eligible for UK visa sponsorship.
- Why this job: Make a real impact in drug development while working with cutting-edge strategies and technologies.
- Qualifications: University degree in medical or biological sciences; 10+ years in the pharmaceutical industry required.
The predicted salary is between 54000 - 84000 £ per year.
The Global Clinical Operations Program Director (GPD) is a core global role within the Clinical Operations function of Late Stage R&D (BioPharmaceuticals and Oncology). The span of responsibilities is broad and may support one or several products depending on scope and complexity. The products supported will be in Phase 3 development or on the market, but the program may include studies in all phases of drug development. On behalf of the Senior Global Clinical Operations Program Director (Sr GPD), the GPD provides strategic operational leadership and oversight of a suite of global clinical studies within a program covering all clinical program deliverables, covering all clinical operations deliverables to scope, quality, budget, time, resource, and risk, ensuring new innovative design and delivery models are used appropriately. The role involves integrating strategy, design, feasibility and operational planning to produce business-focused clinical drug development programs that align with priorities and strategy.
The GPD will develop the core clinical operations components for governance interactions with the oversight of the Sr GPD. The GPD may also act as the lead for crossfunctional teams in delivery of clinical program team (CPT) activities assigned. The GPD may provide project leadership for cross-functional clinical submission teams in support of regulatory marketing applications and post-registration product maintenance deliverables. Additionally, the GPD may lead or contribute to improvement and change projects within clinical operations and/or other business areas.
We are looking for a senior-level professional to lead the development of a regulatory program in collaboration with the sponsor and IQVIA. The primary responsibility will be project management, ensuring effective coordination and execution across all stakeholders. Prior experience in clinical trial development is essential, as the selected candidate will define regulatory processes, oversee implementation, and prepare key documentation aligned with the new structure.
Responsabilities:
- Lead cross-functional teams of experts in the planning and delivery of a defined clinical program of studies and/or clinical activities to scope, quality, budget, time, planning the resource and managing risk.
- Work closely with global study leaders to provide appropriate strategic oversight of a program of studies on behalf of Sr GPD and Clinical Program Team (CPT)
- Provide clinical operations expertise into the project (e.g. country selection, feasibility, operational input into design, risks and external partner management) using new innovative design and delivery models to support governance interactions and project start-up.
- Responsible for providing clinical operations expertise into the development of new business case opportunities for review by governance bodies (cost, timelines, quality, feasibility, risk) On behalf of CPT, responsible for managing clinical plans (cost, FTEs and timelines) in business reporting system, such as PLANIT
- Lead large or complex deliverables and the process to identify and solve/escalate operational issues and drive delivery to plan through internal or external partners (Alliance partners, Clinical Research Organizations (CROs), vendors and Academic Research Organizations (AROs)).
- Act as the sponsor point of escalation for study teams for external (e.g. CRO) partners for externally managed/outsourced studies as appropriate Responsible for leadership and program management of non-drug project work as assigned, e.g. cross functional improvement/change initiatives
- Provide project leadership & management to cross functional Clinical Submission Teams in planning and execution of clinical contribution to Marketing Applications (aligning closely with other key contributors to submission package)
- Lead cross-functional teams in delivery of assigned clinical program team (CPT) activities
- Contribute to functional and cross-functional initiatives as Subject Matter Experts
- Mentor, coach and support people development as appropriate.
- Actively participate in networking both within and outside the therapeutic area, sharing best practises and lesson learnt
- Be an early adopter for new ways of working and act as ambassadors for change, driving the implementation and utilization of new initiatives
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Advanced degree is preferred.
- At least 10 from within the pharmaceutical industry or similar large multinational organizations.
- Proven knowledge of project management tools and processes
- Proven experience in clinical development/drug development process in various phases of development and therapy areas.
- Proven ability to learn by working in multiple phases, TAs, and/or different development situations.
- Experience from leading clinical projects and deliverables or similar expertise from other areas of drug development (such as pharmaceutical development).
- Ability to mentor, develop and educate staff
- Proven leadership promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives
- Skilled & experienced in change management
- Ability to look for and champion more efficient and effective methods/processes of delivering clinical operations components focusing on key performance metrics around reliability, productivity, cost, and quality
- Excellent written and verbal communication skills, negotiation, collaboration and interpersonal skills with ability to work effectively with others at all levels of the organization
- Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a regional and local environment
- Integrity and high ethical standards
- Excellent stakeholder management skills
- Adaptability
- Regulatory submission experience
- Proven knowledge of clinical operations
- Experience with development and implementation of digital health initiatives in Clinical Studies
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at #J-18808-Ljbffr
Associate Global Clinical Operations Director - Sponsor Dedicated in Reading employer: IQVIA, Inc.
IQVIA is an exceptional employer that prioritises innovation and employee development within the dynamic field of clinical operations. With a strong commitment to fostering a collaborative work culture, employees benefit from extensive growth opportunities, mentorship, and the chance to lead impactful projects that shape the future of healthcare. Located in a vibrant area, IQVIA offers a stimulating environment where professionals can thrive while making meaningful contributions to global health advancements.
StudySmarter Expert Advice🤫
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We think you need these skills to ace Associate Global Clinical Operations Director - Sponsor Dedicated in Reading
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at IQVIA, Inc.!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show IQVIA, Inc. that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at IQVIA, Inc.!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At IQVIA, Inc., we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at IQVIA, Inc.
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at IQVIA, Inc. that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with IQVIA, Inc.’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
