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- Tasks: Oversee clinical trial data quality and integrity for oncology-focused studies.
- Company: Proclinical, a leading life sciences recruiter with a global reach.
- Benefits: Remote work flexibility, competitive pay, and opportunities for professional growth.
- Why this job: Make a real impact in clinical trials while working with cutting-edge data management practices.
- Qualifications: Bachelor's degree in relevant field; experience with clinical data programming preferred.
- Other info: Dynamic role with occasional travel to London or Egham, Surrey.
The predicted salary is between 36000 - 60000 £ per year.
Proclinical is seeking a Contract Clinical Data Manager to support oncology-focused clinical trials. In this role, you will oversee the quality and integrity of clinical trial data, ensuring compliance with regulatory standards, internal SOPs, and industry best practices. This is a 6-month contract role, primarily remote, with occasional travel to London or Egham, Surrey, as needed.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Design, set up, and validate EDC systems, including defining and maintaining eCRFs, edit checks, and data management plans.
- Collaborate with CRO partners on database build, validation plans, and data transfer specifications.
- Perform ongoing data review, validation, and query management to ensure data accuracy and completeness.
- Reconcile data across multiple sources, including EDC, safety, labs, imaging, and pharmacovigilance, and support SAE reconciliation.
- Manage medical coding of adverse events, medical history, and medications using MedDRA and WHODrug.
- Ensure compliance with CDISC-CDASH-SDTM standards and internal guidelines.
- Act as the primary Data Management contact for studies, liaising with internal teams, CROs, and site staff.
- Support data preparation for DMCs, interim analyses, and database lock activities.
- Maintain audit-ready documentation and ensure adherence to ICH-GCP, 21 CFR Part 11, and company SOPs.
- Author and maintain Data Management-related SOPs.
Key Skills and Requirements:
- Bachelor\’s degree in Life Sciences, Computer Science, Data Science, or a related field (Master\’s preferred).
- Proficiency in coding dictionaries such as MedDRA and WHODrug, with familiarity in CDISC-CDASH-SDTM standards.
- Strong understanding of drug development phases (I-IV) and clinical trial processes.
- Experience in clinical data programming and the ability to review and evaluate clinical data.
- Excellent communication, problem-solving, and organizational skills.
- Agile thinker with a growth mindset and the ability to adapt to high-speed changes.
- Results-oriented with strong strategic thinking and planning capabilities.
- General data management skills, including maintaining GxP compliance and following standard operating procedures.
If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at h.hennigan@proclinical.com.
Apply Now:
If you are interested in applying to this exciting opportunity, then please click \’Apply\’ or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you\’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.proclinical.com/privacy-policy
Contract Clinical Data Manager employer: Proclinical Staffing
Contact Detail:
Proclinical Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Contract Clinical Data Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical data management field. Attend industry events or webinars, and don’t be shy about asking for introductions. We all know someone who knows someone, so leverage that!
✨Tip Number 2
Prepare for those interviews! Research the company and the role thoroughly. Think about how your skills in EDC systems and data management align with their needs. We want you to shine, so practice common interview questions and have your own ready to go!
✨Tip Number 3
Showcase your expertise! Create a portfolio or a presentation that highlights your experience with clinical trials, data integrity, and compliance standards. We love seeing real examples of your work, so make it easy for them to see what you can bring to the table.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, if you have any questions, we’re here to help. Just reach out, and let’s get you on the path to landing that Contract Clinical Data Manager role!
We think you need these skills to ace Contract Clinical Data Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Contract Clinical Data Manager role. Highlight your experience with EDC systems, data management, and compliance with regulatory standards. We want to see how your skills match 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 oncology-focused clinical trials and how your background makes you a perfect fit for this role. We love seeing enthusiasm and a personal touch.
Showcase Relevant Experience: When filling out your application, be sure to showcase any relevant experience you have with MedDRA, WHODrug, and CDISC standards. We’re keen on candidates who can demonstrate their understanding of clinical trial processes and data integrity.
Apply Through Our Website: Don’t forget to apply through our website! It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, if you have any questions, you can reach out directly to our team!
How to prepare for a job interview at Proclinical Staffing
✨Know Your Data Inside Out
Make sure you’re well-versed in the specifics of clinical data management, especially regarding EDC systems and coding dictionaries like MedDRA and WHODrug. Brush up on your knowledge of CDISC-CDASH-SDTM standards, as this will show your potential employer that you’re not just familiar with the basics but can also handle the complexities of the role.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experiences where you successfully tackled challenges in data management or clinical trials. This could involve resolving discrepancies in data or improving processes. Being able to articulate these situations will demonstrate your analytical thinking and adaptability, which are crucial for this position.
✨Communicate Clearly and Confidently
Since this role involves liaising with various teams and CROs, practice articulating your thoughts clearly. You might want to simulate a few scenarios where you explain complex data issues or project updates. Good communication skills can set you apart, so don’t underestimate their importance!
✨Be Ready for Regulatory Questions
Familiarise yourself with ICH-GCP guidelines and 21 CFR Part 11 compliance. Prepare to discuss how you’ve ensured adherence to these regulations in your previous roles. Showing that you understand the regulatory landscape will reassure the interviewers that you can maintain audit-ready documentation and uphold high standards.
