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- Tasks: Ensure accuracy of clinical trial data and collaborate with teams to maintain high-quality databases.
- Company: Join Quotient Sciences, a leader in drug development and manufacturing.
- Benefits: Competitive salary, diverse workplace, and opportunities for professional growth.
- Other info: Dynamic environment with a commitment to diversity and inclusion.
- Why this job: Make a real impact in healthcare by accelerating drug development for patients.
- Qualifications: Life sciences degree preferred; strong organisational and communication skills required.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.
Our proprietary platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process, reducing costs, improving outcomes, and significantly accelerating drug development times.
We are looking for a Data Manager III to join our team in Edinburgh and play a key role in ensuring the accuracy and consistency of clinical trial data. You will work closely with internal teams and sponsors to maintain high-quality clinical databases in compliance with study protocols, Data Management Plans, SOPs, and regulatory guidelines.
Data Sciences at Quotient Sciences comprises six departments (including Data Management) and over 100 staff, providing an expert service in the data management, analysis, and reporting of early phase clinical studies.
Main Tasks And Responsibilities:
- Act as Lead Data Manager for assigned studies under supervision
- Represent Data Management at multi-departmental meetings
- Develop and maintain Data Management Plans
- Review clinical database build documentation and perform user acceptance testing (UAT)
- Create and finalise Edit Check Specifications
- Conduct testing of edit checks
- Generate and review data listings
- Manage queries and query resolution
- Perform reconciliation of data from external vendors
- Generate Data Management Reviews and provide feedback to relevant departments
- Use eTMF to maintain Data Management study documentation
- Train, mentor, and provide oversight of junior Data Management team members
Qualifications And Experience Required For Competent Performance:
- Life sciences degree is preferable but not essential
- Good organisational skills
- Ability to work to deadlines and multitask in a fast-paced environment whilst maintaining quality standards
- Effective oral and written communication skills
- High attention to detail
- Working knowledge of GCP and relevant regulatory guidance
- Logical thinking and problem-solving abilities
Application Requirements:
When applying for a position with Quotient Sciences, you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred, then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion:
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, and working conditions.
Clinical Data Associate in Edinburgh employer: Quotient Sciences
Contact Detail:
Quotient Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Data Associate in Edinburgh
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with yours. This will help you stand out and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice your responses to common interview questions. Use the STAR method (Situation, Task, Action, Result) to structure your answers. This will help you articulate your experiences clearly and effectively.
✨Tip Number 4
Don’t forget to follow up after your interview! A simple thank-you email can go a long way in leaving a positive impression. Plus, it shows your enthusiasm for the role and keeps you on their radar.
We think you need these skills to ace Clinical Data Associate in Edinburgh
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Data Associate role. Highlight relevant experience and skills that match the job description. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about joining Quotient Sciences and how you can contribute to our mission. Keep it concise but impactful!
Showcase Your Attention to Detail: Since this role requires high attention to detail, make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best work right from the start.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Quotient Sciences
✨Know Your Stuff
Make sure you brush up on your knowledge of GCP and relevant regulatory guidelines. Being able to discuss these topics confidently will show that you're serious about the role and understand the importance of compliance in clinical data management.
✨Showcase Your Organisational Skills
Prepare examples from your past experiences where you've successfully managed multiple tasks or projects under tight deadlines. Quotient Sciences values efficiency, so demonstrating your ability to multitask while maintaining quality will set you apart.
✨Communicate Clearly
Practice articulating your thoughts clearly and concisely. Effective communication is key in this role, especially when liaising with internal teams and sponsors. Consider doing mock interviews to refine your delivery and ensure you can convey complex information simply.
✨Attention to Detail is Key
Be ready to discuss how you've maintained high standards of accuracy in your previous roles. Prepare to share specific instances where your attention to detail made a significant impact, as this is crucial for ensuring the integrity of clinical trial data.