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- Tasks: Manage and validate clinical trial data while coordinating with teams.
- Company: Join a growing biotech firm revolutionising cancer diagnostics in Cambridge.
- Benefits: Enjoy a thriving culture, skill development, and a purpose-driven environment.
- Why this job: Make an immediate impact in oncology while working with like-minded individuals.
- Qualifications: PhD or MSc in STEM; experience with EDC systems preferred.
- Other info: Full-time role, 3 days onsite in South Cambridge.
The predicted salary is between 36000 - 60000 £ per year.
SciPro are partnered with a growing biotech company developing an innovative new era of cancer diagnostics. They are looking for a Clinical Data Manager/Data Coordinator to support ongoing clinical studies by managing trial data and coordinating with clinical and laboratory teams.
Responsibilities:
- Clean, standardise, and validate clinical trial data.
- Build, manipulate and maintain study databases.
- Ensure data quality and compliance with GCP and data protection standards, and TMF.
- Liaise with and train trial and lab staff for accurate data collection.
- Assist with regulatory submissions and documentation.
- Support training of trial personnel on data processes.
Requirements:
- PhD or MSc in a STEM field (e.g. Bioinformatics, Statistics, Engineering etc).
- Hands-on experience with Electronic Data Capture (EDC) systems. Medidata Rave would be a plus.
- Track record of working with clinical trial data and documentation. Colorectal or Gynae cancer would be a plus.
- Knowledge of GCP and GDPR for clinical data.
Desirable:
- Programming skills (Python, R) and version control (Git).
- Trial site monitoring or coordination experience.
This is a full-time, permanent role, 3 days a week onsite in South Cambridge.
Clinical Data Manager / Data Coordinator employer: SciPro
Contact Detail:
SciPro Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Data Manager / Data Coordinator
✨Tip Number 1
Familiarise yourself with Electronic Data Capture (EDC) systems, especially Medidata Rave, as this is a key requirement for the role. Consider taking online courses or tutorials to enhance your skills and demonstrate your commitment to mastering these tools.
✨Tip Number 2
Network with professionals in the oncology diagnostics field. Attend relevant conferences or webinars to connect with industry experts and learn about the latest trends. This can help you gain insights into the role and potentially get referrals.
✨Tip Number 3
Brush up on your knowledge of Good Clinical Practice (GCP) and General Data Protection Regulation (GDPR). Being well-versed in these regulations will not only boost your confidence but also show potential employers that you understand the importance of compliance in clinical trials.
✨Tip Number 4
If you have programming skills in Python or R, make sure to highlight them during your discussions. These skills are increasingly valuable in data management roles, and showcasing them can set you apart from other candidates.
We think you need these skills to ace Clinical Data Manager / Data Coordinator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical data management and any hands-on experience with Electronic Data Capture (EDC) systems. Emphasise your educational background in a STEM field and any specific projects related to oncology diagnostics.
Craft a Strong Cover Letter: In your cover letter, express your passion for oncology diagnostics and how your skills align with the responsibilities of the role. Mention your familiarity with GCP and GDPR, and provide examples of how you've ensured data quality in previous roles.
Highlight Technical Skills: If you have programming skills in Python or R, make sure to include these in your application. Discuss any experience with version control systems like Git, as this could set you apart from other candidates.
Showcase Relevant Experience: Detail any previous roles where you managed clinical trial data or coordinated with clinical teams. If you have experience in colorectal or gynae cancer studies, be sure to mention this as it is a plus for the position.
How to prepare for a job interview at SciPro
✨Showcase Your Technical Skills
Make sure to highlight your hands-on experience with Electronic Data Capture (EDC) systems, especially if you have worked with Medidata Rave. Be prepared to discuss specific projects where you utilised these skills.
✨Demonstrate Knowledge of GCP and GDPR
Since compliance is crucial in clinical data management, be ready to explain your understanding of Good Clinical Practice (GCP) and General Data Protection Regulation (GDPR). Provide examples of how you've ensured data quality and compliance in past roles.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world scenarios. Think about challenges you've faced in managing clinical trial data and how you overcame them, particularly in relation to data cleaning and validation.
✨Emphasise Team Collaboration
This role involves liaising with various teams, so be sure to discuss your experience in collaborating with clinical and laboratory staff. Share examples of how you’ve trained others on data processes and ensured accurate data collection.
