At a Glance
- Tasks: Lead drug development studies and ensure high-quality data delivery.
- Company: Top contract research organisation in the heart of Cambridge.
- Benefits: Competitive salary, career growth, and a chance to make a difference.
- Other info: On-site role with opportunities for professional development.
- Why this job: Join a dynamic team and contribute to groundbreaking scientific research.
- Qualifications: Degree in Biological Sciences and experience in a GxP lab.
The predicted salary is between 35000 - 42000 £ per year.
Location: Cambridge, England, United Kingdom (On-site)
About the Company
A leading contract research organisation is looking for a skilled scientist or study coordinator to step into the role of study manager and support in the delivery of client drug development studies. The study manager will be someone with good organisation understanding of molecular techniques such as ELISA, MSD as well as being experienced working in a regulated environment.
Responsibilities
- Lead end-to-end delivery of regulated studies (GLP/GCP).
- Make robust scientific decisions aligned with EMA and FDA guidance.
- Oversee method validation and sample analysis with scientific authority.
- Act as primary client contact, building strong partnerships and supporting programme progression.
- Ensure timely delivery of high-quality data and study reports.
Qualifications
- Degree in Biological Sciences, Biochemistry, Immunology, or related field.
- Experience in a GxP laboratory (GLP/GCP preferred).
- Knowledge of immunoassay platforms (e.g. ELISA, LBA, MSD) is advantageous.
- Strong understanding of EMA/FDA bioanalytical validation guidelines.
- Excellent communication skills with ability to present scientific data clearly.
Salary - (35,000 to 42,000 DOE)
Study Manager — GLP/GCP Data & Client Lead in Cambridge employer: United Cerebral Palsy of Georgia
As a leading contract research organisation based in Cambridge, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we offer numerous growth opportunities and support for continuous learning, ensuring that our team members thrive in a dynamic environment dedicated to advancing drug development. Join us to be part of a mission-driven team where your contributions directly impact client success and scientific progress.
Contact Details:
United Cerebral Palsy of Georgia Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Study Manager — GLP/GCP Data & Client Lead in Cambridge
✨Tip Number 1
Network like a pro! Reach out to professionals in the industry on LinkedIn or at local events. We can’t stress enough how important it is to build connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to study management. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your expertise! Bring along examples of your previous work or case studies that highlight your experience in GLP/GCP environments. We want to see how you’ve made an impact in your past roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Study Manager — GLP/GCP Data & Client Lead in Cambridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Study Manager role. Highlight your experience in GLP/GCP environments and any relevant molecular techniques like ELISA or MSD. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the role and how your skills can help us deliver high-quality data and reports. Don't forget to mention your experience with client interactions!
Showcase Your Scientific Knowledge:In your application, demonstrate your understanding of EMA and FDA guidelines. We’re keen on candidates who can make robust scientific decisions, so share examples of how you've done this in past roles.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from us during the process!
How to prepare for a job interview at United Cerebral Palsy of Georgia
✨Know Your Science
Brush up on your knowledge of molecular techniques like ELISA and MSD. Be ready to discuss how you've applied these methods in previous roles, especially in a regulated environment. This will show that you understand the technical aspects of the job.
✨Understand Regulatory Guidelines
Familiarise yourself with EMA and FDA guidelines related to GLP/GCP studies. Being able to reference specific regulations during your interview will demonstrate your expertise and commitment to compliance, which is crucial for this role.
✨Showcase Your Communication Skills
Prepare to discuss how you've effectively communicated scientific data in the past. Think of examples where you’ve built strong partnerships with clients or colleagues, as this role requires excellent communication to support programme progression.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Prepare examples of how you've made robust scientific decisions under pressure, ensuring you can articulate your thought process clearly.
