At a Glance
- Tasks: Manage clinical data activities and ensure accuracy in a fast-paced environment.
- Company: Join a leading biotech firm focused on innovative cancer therapies.
- Benefits: Enjoy a competitive salary, hybrid work options, and comprehensive benefits.
- Other info: Opportunities for growth in a well-funded company with major pharmaceutical partnerships.
- Why this job: Make a real impact in cancer treatment while working with cutting-edge science.
- Qualifications: Bachelor's degree in relevant field and experience in clinical data management required.
The predicted salary is between 43200 - 72000 £ per year.
Carrot Recruitment are acting as a recruitment agency on the sourcing of a Clinical Data Manager for a clinical-stage biotechnology company at the forefront of cancer drug development. Our client combines cutting-edge science with a patient-centric approach, offering a dynamic and mission-driven work environment. With recent strategic investments from major pharmaceutical partners, the company is well-funded and poised for significant growth.
This is a unique opportunity to contribute to the development of transformational therapies that aim to improve the lives of people with difficult-to-treat cancers who are classified as a top biotech to watch in this space.
Everything you need to know about the role:
- As the Clinical Data Manager, you’ll have significant recent experience of managing all activities related to clinical data, and at all stages of process.
- You will be responsible for all elements of the clinical data management and be able to showcase your ability to work in an agile and fast-paced environment, with integrity and accuracy.
- Serve as the lead Data Manager on a study level and contribute to the design of the eCRF, collection of data and review of data for accuracy and completeness.
- Interact with members of the multidisciplinary project teams to provide ongoing data management support for clinical trials.
- Familiarity with risk-based data management process.
- Oversee database builds, including UAT, ensuring data integrity and security.
- Participate in the development and implementation of the standard processes and guidelines for the DM function.
- Management of data management tasks, on a study level performed by the vendor, in adherence with established standards including third party vendor data reconciliation, protocol deviation collection, SAE reconciliation and data issue resolution.
- Coordinate internal cross-functional review of data management documents, as required.
- Stay abreast of new and/or evolving local regulations, guidelines and policies related to clinical development.
Experience and qualities that make you a strong fit:
- Bachelor’s degree in computer science, life sciences or equivalent.
- Recent relevant experience in a Clinical Data role.
- Current and up-to-date GCP training.
- Experience in setting up EDC systems is essential, and vendor management experience preferred.
- Experience in oncology essential, multiple myeloma preferred.
- In-depth understanding of clinical trial processes and involved functional stakeholders.
- Knowledge of FDA, EMA and ICH regulations/guidelines and the drug development process is preferred but not essential.
- Proficient in Excel.
What’s on offer?
- A competitive salary.
- Comprehensive benefits package, including medical insurance, pension, bonus and share scheme.
- Hybrid working model (Manchester location preferred, although commuting distance Cambridge/London would also be possible).
- Opportunities to be part of a fast-growing biotech at a significant part of their development.
Could this be the role for you?
If you’re ready to take on this exciting opportunity and bring your expertise to a company that’s listed as one to watch, we’d love to hear from you. Please apply with your most recent CV, to be considered.
Clinical Data Manager in Nottingham employer: LinkedIn
Join a pioneering clinical-stage biotechnology company that is dedicated to transforming cancer treatment through innovative therapies. With a strong focus on employee growth and a collaborative work culture, you will thrive in a dynamic environment that values integrity and accuracy. Enjoy a competitive salary, comprehensive benefits, and the flexibility of a hybrid working model, all while contributing to meaningful advancements in oncology.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Data Manager in Nottingham
✨Tip Number 1
Network with professionals in the biotechnology and clinical data management fields. Attend industry conferences, webinars, or local meetups to connect with potential colleagues and learn about the latest trends in cancer drug development.
✨Tip Number 2
Familiarise yourself with the specific EDC systems mentioned in the job description. If you have experience with any particular platforms, be ready to discuss how you've used them effectively in past roles during interviews.
✨Tip Number 3
Stay updated on the latest regulations and guidelines related to clinical trials, especially those from the FDA, EMA, and ICH. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality in clinical data management.
✨Tip Number 4
Prepare to showcase your experience in managing clinical data processes. Think of specific examples where you successfully led data management tasks or resolved data issues, as these will be crucial talking points during your interview.
We think you need these skills to ace Clinical Data Manager in Nottingham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in clinical data management, especially any work related to oncology or EDC systems. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter:Write a cover letter that showcases your passion for cancer drug development and your understanding of the company's mission. Mention specific experiences that align with the responsibilities of the Clinical Data Manager position.
Highlight Relevant Skills:In your application, emphasise your proficiency in Excel and any experience you have with risk-based data management processes. This will show that you possess the technical skills necessary for the role.
Showcase Your Teamwork Abilities:Since the role involves interacting with multidisciplinary project teams, include examples of how you've successfully collaborated with others in previous roles. This will demonstrate your ability to thrive in a dynamic environment.
How to prepare for a job interview at LinkedIn
✨Showcase Your Clinical Data Experience
Make sure to highlight your recent experience in managing clinical data. Be prepared to discuss specific projects you've worked on, particularly those involving eCRF design and data accuracy, as this will demonstrate your capability to handle the responsibilities of the role.
✨Understand the Company’s Mission
Research the biotechnology company’s mission and recent developments in cancer drug development. Showing that you align with their patient-centric approach and are passionate about improving lives can set you apart from other candidates.
✨Familiarise Yourself with Regulations
Brush up on FDA, EMA, and ICH regulations related to clinical trials. Even if not essential, demonstrating knowledge of these guidelines can show your commitment to compliance and understanding of the drug development process.
✨Prepare for Agile Environment Questions
Expect questions about your ability to work in a fast-paced and agile environment. Prepare examples from your past experiences where you successfully adapted to changes or managed multiple tasks efficiently, as this is crucial for the role.
