At a Glance
- Tasks: Lead clinical research studies and ensure data quality across multiple sites.
- Company: Join Roche, a leader in healthcare innovation and diagnostics.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on collaboration and continuous improvement.
- Why this job: Make a real impact on patient care and advance healthcare solutions globally.
- Qualifications: Bachelor's degree in a scientific field and experience in clinical lab coordination.
The predicted salary is between 46000 - 52000 £ per year.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
At Roche Diagnostics Solutions (RDS), our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient is unique. Our Clinical Development & Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally. We see ourselves and our customers as a team that can only reach its full potential together. By listening closely to patients and physicians, and leveraging digitalisation and new technologies, we get closer to their real-world needs. This collaborative spirit creates an environment where ideas can grow and new ways of doing things can be tried - resulting in competitive products that get to patients faster.
Our work spans the entire product lifecycle, from discovery to post-launch. By collaborating with internal teams, external partners, and patients, the CDMA chapter provides crucial medical insights, designs and executes clinical studies, and offers on-market support. Ultimately, we generate the comprehensive clinical evidence that demonstrates product safety, effectiveness, and scientific validity - facilitating smooth product registration, adoption and reimbursement globally so we can save lives and improve patient quality of life.
The Opportunity
As a Clinical Site Manager specialising in our molecular lab portfolio, you will be responsible for designing, planning, coordinating, and conducting clinical research studies across assigned sites. Working independently, you will serve as the primary clinical trial expert, ensuring data generation methodologies are delivered in alignment with global quality protocols. This role offers an exciting opportunity to validate product performance claims, supply crucial data for regulatory submissions, and directly help deliver innovative diagnostic solutions to patients worldwide.
Key Responsibilities:
- Lead Site Execution: Act as the primary contact and clinical trial expert for assigned study site personnel, delivering technical assistance and coordinating necessary training.
- Conduct Site Assessments: Perform comprehensive site assessments and qualification visits to drive informed site selection decisions.
- Manage Site Activation: Collaborate cross-functionally to ensure investigational sites properly obtain and maintain institutional approvals and meet all regulatory compliance needs before trial initiation.
- Develop Essential Documentation: Author and review key study site documents, including Study Monitoring Plans, informed consent forms, and case report forms, while contributing technical expertise to study protocols.
- Deliver End-to-End Monitoring: Execute all data generation, data validation, and comprehensive site visits across all study phases, from start-up through to close-out.
- Partner Cross-Functionally: Work dynamically within local, global, and virtual study teams, collaborating with R&D, Field Service, Study Management, and Biometrics to deliver top-tier solutions.
- Support Process Optimisation: Contribute to continuous improvement and change management activities to bring fresh perspectives to existing diagnostic testing solutions.
Who You Are
You are a proactive, adaptable professional who thrives in a fast-paced, matrixed environment. You bring strong analytical and problem-solving skills, make independent, sound choices, and possess a natural ability to build consensus across diverse teams.
- Education & Lab Familiarity: A Bachelor's degree in a scientific discipline or a related field (or an equivalent combination of education and experience). Hands-on experience in a clinical laboratory or clinical lab study coordination is highly valued.
- Clinical Operations Foundations: Typically brings professional experience, with solid conceptual and practical knowledge of clinical operations or diagnostic product development.
- Regulatory Compliance: Good knowledge of, and strict adherence to, clinical trial and laboratory standards, including ICH-GCP guidelines, FDA Regulations, and IVDR.
- Global Collaboration: Proven ability to partner across diverse regions, cultures, and time zones to cultivate an environment of belonging, inclusion, and diversity.
- Communication Skills: Exceptional verbal and written communication skills in English, allowing you to explain complex data clearly in straightforward situations.
Ready to make a difference? Help us achieve our ambition: to advance science, so that we all have more time with the people we love. Apply today and help us shape the future of healthcare!
Clinical Site Manager (Molecular Lab) in Burgess Hill employer: F. Hoffmann-La Roche AG
At Roche, we pride ourselves on fostering a culture of inclusivity and collaboration, where every employee is valued for their unique contributions. As a Clinical Site Manager in our molecular lab, you will benefit from a supportive work environment that encourages personal growth and professional development, alongside the opportunity to make a meaningful impact on global healthcare outcomes. With a commitment to innovation and excellence, Roche offers competitive benefits and a dynamic workplace that empowers you to thrive in your career while helping to improve patient lives.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Site Manager (Molecular Lab) in Burgess Hill
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Roche through LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research Roche’s latest projects in molecular diagnostics and think about how your experience aligns with their mission. Show them you’re not just another candidate!
✨Tip Number 3
Practice makes perfect! Get a friend to do mock interviews with you. Focus on articulating your clinical operations experience and how you can contribute to Roche’s goals. Confidence is key!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the Roche team. Let’s get you that job!
We think you need these skills to ace Clinical Site Manager (Molecular Lab) in Burgess Hill
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Site Manager role. Highlight your relevant experience in clinical research and any specific skills that align with the job description. We want to see how you can bring value to our team!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about this role and how your background makes you a perfect fit. Be genuine and let your personality come through – we love authenticity!
Showcase Your Communication Skills:Since communication is key in this role, make sure your application reflects your ability to convey complex information clearly. Whether it's in your CV or cover letter, we want to see how you articulate your thoughts and ideas.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at F. Hoffmann-La Roche AG
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical operations and molecular lab processes. Familiarise yourself with ICH-GCP guidelines and FDA regulations, as these will likely come up in conversation. Being able to discuss these topics confidently will show that you're serious about the role.
✨Show Your Collaborative Spirit
Roche values teamwork, so be prepared to share examples of how you've successfully collaborated with diverse teams in the past. Think of specific instances where your communication skills helped bridge gaps or resolve conflicts. This will demonstrate your ability to thrive in a matrixed environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical trials and how they integrate new technologies. This not only shows your interest in the role but also your understanding of the industry's direction. It’s a great way to engage with your interviewers and leave a lasting impression.
✨Be Yourself
Roche encourages personal expression, so don’t hesitate to let your personality shine through. Share your unique qualities and experiences that make you a good fit for the team. Authenticity can set you apart from other candidates and help you connect with the interviewers on a personal level.
