Perspectum Ltd
Clinical Data Manager I
Get notified of more jobs like this · No spam, ever
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Job Overview
The Clinical Data Manager I is responsible for ensuring that clinical trial data is accurate, complete, and consistent with study protocol, standard operating procedures (SOPs), and regulatory requirements. They work closely with cross-functional teams, including clinical operations, biostatistics, and medical writing, to support the collection, management, and analysis of clinical trial data. They are a detail-oriented individual with a passion for clinical research and data management.
Essential Duties and Responsibilities
- EDC data entry and review.
- Generating data queries and performing data validation on reconciliation.
- Assist with database lock requests.
- Monitor the progress of data cleaning activities and the quality of the data.
- Assist in database design, set up, testing, and maintenance.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Desirable
Get help with your application
Your very own career expert that helps elevate your application to the next level.
- Assist with Data Transfer Agreements and Data Management Plan drafting.
- Manage EDC access.
- Database design, set up, testing, and maintenance.
- Oversee/execute database lock requests.
- Ensure CDM activities conform to ICH GCP guidance.
- Lead and/or participate in internal and external audits of clinical data management processes.
Person Specification
Essential
- Bachelor’s degree in a relevant field (i.e., Life Sciences, Engineering, etc).
- Strong organisation and prioritising skills with ability to meet multiple deadlines.
- Excellent attention to detail and accuracy.
- Excellent communication and collaboration skills.
- Passion for working with data / clinical research / clinical trials.
Desirable
- Advanced degree in a relevant field (i.e., Life Sciences, Engineering, etc).
- Certificate in Good Clinical Practise (GCP).
- Experience in CDM and knowledge of effective clinical data management practices.
- Knowledge of effective clinical data management practices.
- Experience working with Clinical Data Management and Electronic Data Capture (EDC) systems.
- Knowledge of Good Clinical Data Management Practices (GCDMP) and CDISC Study Data Tabulation Model (SDTM) standards.
- Experience within Medical Devices/Pharma/Clinical industry.
- Strong project and resource management skills with ability to manage multiple projects.
- Experience working with Quality Framework (ISO) standards (e.g., ISO27001, ISO13485) and ICH GCP, and understanding of 21 CFR Part 11 regulation.
- Proactive, analytical, and problem-solving skills with commitment for continuous improvement.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills
Location