Global Clinical Data Manager - Submissions & Oversight
Global Clinical Data Manager - Submissions & Oversight

Global Clinical Data Manager - Submissions & Oversight

Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Oversee vendor activities and ensure quality of clinical data deliverables.
  • Company: Leading clinical research organisation in Greater London.
  • Benefits: Competitive salary, professional development, and a dynamic work environment.
  • Why this job: Make a real impact in drug development and enhance your project management skills.
  • Qualifications: 8+ years in data management with expertise in clinical trials required.
  • Other info: Ideal for those seeking to advance their career in a fast-paced industry.

The predicted salary is between 48000 - 72000 £ per year.

A leading clinical research organization in Greater London seeks an experienced professional for a data management role. The candidate will oversee vendor activities, ensure quality and compliance of data deliverables, and manage external budgets.

Advanced knowledge of drug development processes and strong project management skills are required. The role demands a minimum of 8 years in data management with expertise in clinical trials. A master's or bachelor's degree in a related field is essential, alongside a proven track record of managing complex programs.

Global Clinical Data Manager - Submissions & Oversight employer: Cytel (EMEA)

As a leading clinical research organisation in Greater London, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel. We offer competitive benefits, including professional development opportunities and a supportive environment that encourages growth and advancement within the industry. Join us to be part of a team that is dedicated to making a meaningful impact in clinical research while enjoying the vibrant atmosphere of one of the world's most dynamic cities.
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Contact Detail:

Cytel (EMEA) Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Clinical Data Manager - Submissions & Oversight

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for a Global Clinical Data Manager role. 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 brushing up on your project management skills and drug development processes. We recommend practising common interview questions related to data management and compliance, so you can showcase your expertise confidently.

✨Tip Number 3

Don’t just apply anywhere; focus on organisations that align with your values and career goals. Use our website to find roles that excite you and match your experience in clinical trials. Tailor your approach to each application for the best results!

✨Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. It shows your enthusiasm for the role and gives you another chance to highlight why you’re the perfect fit for the position.

We think you need these skills to ace Global Clinical Data Manager - Submissions & Oversight

Data Management
Vendor Oversight
Quality Assurance
Compliance Management
Budget Management
Drug Development Processes
Project Management
Clinical Trials Expertise
Complex Program Management
Bachelor's Degree
Master's Degree

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in data management and clinical trials. We want to see how your skills align with the role, so don’t be shy about showcasing your relevant achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Global Clinical Data Manager position. Share specific examples of your project management skills and how you've ensured quality and compliance in past roles.

Showcase Your Knowledge: We’re looking for someone with advanced knowledge of drug development processes. Make sure to mention any relevant certifications or training that demonstrate your expertise in this area. It’ll help us see you as a strong candidate!

Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about what we do at StudySmarter!

How to prepare for a job interview at Cytel (EMEA)

✨Know Your Stuff

Make sure you brush up on your knowledge of drug development processes and clinical trials. Be ready to discuss specific examples from your past experience that demonstrate your expertise in data management and project oversight.

✨Vendor Management Insights

Since the role involves overseeing vendor activities, think about how you've successfully managed vendor relationships in the past. Prepare to share strategies you've used to ensure quality and compliance in data deliverables.

✨Budget Savvy

Get familiar with budget management as it’s a key part of the role. Be prepared to discuss how you've handled external budgets in previous positions, including any challenges you faced and how you overcame them.

✨Showcase Your Leadership

With a minimum of 8 years in data management, you’ll want to highlight your project management skills. Think of examples where you led complex programmes and how you ensured successful outcomes. Confidence in your leadership abilities will shine through!

Global Clinical Data Manager - Submissions & Oversight
Cytel (EMEA)

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