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 dynamic work environment.
- Other info: Join a collaborative team and build strong client partnerships.
- Why this job: Make a real impact in drug development while working with cutting-edge science.
- Qualifications: Degree in Biological Sciences or related field; GxP lab experience preferred.
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)
Clinical Study Manager. Job in Cambridge LilyLifestyle Jobs employer: United Cerebral Palsy of Georgia
As a leading contract research organisation based in the vibrant city of Cambridge, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel. With a strong focus on professional development, we offer numerous growth opportunities and support for continuous learning, ensuring that our team members thrive in their careers while contributing to impactful drug development studies. Join us to be part of a dynamic environment where your expertise in molecular techniques will be valued and your contributions will make a real difference in advancing healthcare.
Contact Details:
United Cerebral Palsy of Georgia Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Study Manager. Job in Cambridge LilyLifestyle Jobs
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. Building connections can lead to job opportunities that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GLP/GCP regulations and molecular techniques. We want you to be able to showcase your expertise confidently when discussing your experience with ELISA and MSD.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your career goals. Check out our website for openings that match your skills and interests, and tailor your approach to each one.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Plus, it shows your enthusiasm for the role and the company.
We think you need these skills to ace Clinical Study Manager. Job in Cambridge LilyLifestyle Jobs
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Study Manager role. Highlight your experience with molecular techniques like ELISA and MSD, and any work you've done in regulated environments. 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 passionate about drug development studies and how your skills make you the perfect fit for our team. Don't forget to mention your understanding of EMA and FDA guidelines!
Showcase Your Communication Skills:Since excellent communication is key for this role, make sure to demonstrate your ability to present scientific data clearly in your application. Whether it's in your CV or cover letter, we want to see how you can effectively convey complex information.
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’re considered for the role. Plus, it shows us you’re keen on joining our team at StudySmarter!
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 GLP and GCP regulations, as well as EMA and FDA guidelines. Being able to speak confidently about these will demonstrate your readiness to lead regulated studies and make informed scientific decisions.
✨Showcase Your Communication Skills
Prepare to discuss how you've built strong partnerships with clients in the past. Think of examples where your communication skills helped progress a project or resolve an issue. This is key since you'll be acting as the primary client contact.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving abilities in real-world scenarios. Think about challenges you've faced in study management and how you overcame them. This will help you illustrate your capability to deliver high-quality data and reports.
