Senior Clinical Study Manager in Weybridge

Senior Clinical Study Manager in Weybridge

Weybridge Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Gsk

At a Glance

  • Tasks: Lead clinical studies and collaborate with global medical leaders to enhance operational support.
  • Company: Join Haleon, a purpose-driven consumer health company with a trusted portfolio of brands.
  • Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
  • Other info: Diverse and inclusive workplace committed to employee well-being and development.
  • Why this job: Make a real impact on everyday health while working in a dynamic and innovative environment.
  • Qualifications: Bachelor's degree and 5+ years of project management experience in clinical research.

The predicted salary is between 60000 - 80000 £ per year.

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.

Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

Job Purpose

Are you energised by the opportunity to partner with key leaders in global medical science to enhance global operational support? If so, this Clinical Study Management Manager role could be an exciting opportunity to explore. The role provides operational leadership to the Clinical Study Team and is responsible for the planning, management, execution and delivery of the trial according to study timelines, budget and quality. The role will require robust use of project management tools and operational practices.

Key Responsibilities

  • Exhibits strong study operational strategy to plan and oversee execution of assigned studies, supporting clinical strategy defined in the Non-Clinical & Clinical Development Plan.
  • Acts as Study Team Leader and primary operational contact for 1–3 trials of average design and protocol complexity, including clinical trials, behavioural testing, and decentralised/virtual trials.
  • Has the ability and agility to manage the delivery of any type of study, including complex or unusual study designs, new indications, challenging regional environments and local regulations, while strategically influencing operational delivery.
  • Responsible for the implementation, conduct and tracking of study trials in compliance with ICH/GCP and local regulations, company SOPs and written standards for the conduct of human subject research, study timelines, budget and project specifications.
  • Provides operational and strategic leadership to assure successful delivery of trials, in alignment with Haleon expectations and behaviours.
  • Provides oversight of clinical sites, CROs and vendor activities according to Functional Service Provider (FSP) or Full-Service Outsourcing (FSO) models. Leads or participates in clinical site assessments.
  • Leads the coordination of cross-functional department activities to successfully achieve milestones and quality deliverables in study management, including study start-up, recruitment, study conduct, database lock and study close-out, with risk and issue management and assurance of TMF inspection readiness.
  • Contributes to plans and study documents from an operational standpoint, such as protocols, informed consent forms, monitoring plans, vendor contracts and clinical study reports.
  • Acts as HBS custodian.
  • Takes on functional leadership responsibilities, providing expert consultation for issue resolution and piloting new ways of working.
  • Represents Clinical Operations in vendor and due diligence/audit activities and provides subject matter expertise on implementing Good Clinical Practice, business improvement initiatives and change implementation.

Key Competencies

  • Bachelor’s degree.
  • 5 or more years of industry project management experience.
  • Relevant clinical research or operational specialty training preferred.
  • Experience providing operational support across global scientific and medical functions.
  • Externally facing role experience and technical expertise.
  • Desirable: Advanced degree in Life Sciences.
  • Strong stakeholder management experience.
  • Proven ability to influence and build consensus.

Equal Opportunities

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong.

During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.

Adjustment or Accommodations Request

If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.

Senior Clinical Study Manager in Weybridge employer: Gsk

GSK is an exceptional employer located in Greater London, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior FinOps Product Manager, you will have the opportunity to drive impactful projects while benefiting from robust employee growth opportunities and a culture that values diverse perspectives. With a commitment to professional development and a focus on agile methodologies, GSK empowers its employees to thrive in their careers while contributing to meaningful advancements in cloud financial management.

Gsk

Contact Details:

Gsk Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Clinical Study Manager in Weybridge

Unlock Networking Opportunities

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Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Gsk.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Gsk. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Gsk is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Senior Clinical Study Manager in Weybridge

Project Management
Clinical Study Management
Operational Leadership
Stakeholder Management
Regulatory Compliance (ICH/GCP)
Cross-Functional Coordination
Risk and Issue Management

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 Gsk!

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 Gsk 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 Gsk!

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 Gsk, 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 Gsk

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 Gsk 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 Gsk’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.