At a Glance
- Tasks: Lead clinical research studies and ensure data quality in a dynamic lab environment.
- Company: Join Roche, a leader in healthcare innovation and diagnostics.
- Benefits: Competitive salary, inclusive culture, and opportunities for personal growth.
- Other info: Collaborative team environment with a focus on diversity and inclusion.
- 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 Diagnostics Lab in Motherwell employer: F. Hoffmann-La Roche AG
At Roche, we pride ourselves on fostering a culture of inclusivity and personal expression, where every employee is valued for their unique contributions. As a Clinical Site Manager in our Molecular Diagnostics Lab, you will benefit from a collaborative work environment that encourages innovation and professional growth, while directly impacting patient care through cutting-edge diagnostic solutions. With a commitment to employee development and a focus on meaningful work, Roche offers an exceptional opportunity to thrive in your career while making a difference in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Site Manager – Molecular Diagnostics Lab in Motherwell
✨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 Diagnostics Lab in Motherwell
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Clinical Site Manager role. Highlight any relevant lab experience and clinical operations knowledge to show us you’re the right fit!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about molecular diagnostics and how your background aligns with our mission at Roche. Keep it engaging and personal!
Showcase Your Communication Skills:Since communication is key in this role, make sure your application showcases your ability to convey complex information clearly. Use straightforward language and structure your thoughts logically.
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 ensure it gets the attention it deserves!
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 molecular diagnostics and clinical trial processes. Familiarise yourself with Roche's products and their impact on patient care. This will show that you're genuinely interested and prepared to contribute.
✨Showcase Your Experience
Be ready to discuss your hands-on experience in clinical labs or study coordination. Prepare specific examples of how you've managed site assessments or collaborated cross-functionally. This will help demonstrate your practical knowledge and problem-solving skills.
✨Emphasise Teamwork
Roche values collaboration, so highlight your ability to work within diverse teams. Share instances where you've successfully partnered with others to achieve a common goal, especially in a fast-paced environment. This will resonate well with their team-oriented culture.
✨Ask Insightful Questions
Prepare thoughtful questions about the role and the company's approach to innovation in healthcare. This not only shows your enthusiasm but also helps you gauge if the company culture aligns with your values. It’s a win-win!
