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

Global Clinical Data Manager - Submissions & Oversight in London

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

  • Tasks: Oversee vendor activities and ensure quality compliance in data deliverables.
  • Company: Leading clinical research organisation based in Greater London.
  • Benefits: Competitive salary, professional development, and a dynamic work environment.
  • Why this job: Join a pivotal role in drug development and make a real impact on clinical trials.
  • 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 in London 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, continuous professional development opportunities, and a commitment to work-life balance, making us an excellent employer for those seeking meaningful and rewarding careers in the clinical data management field.
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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 in London

✨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 tailor your approach to each company’s culture and mission.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.

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

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. We love seeing passion and personality, so let us know what excites you about this opportunity.

Showcase Your Project Management Skills: Since strong project management skills are a must, make sure to include specific examples of how you've successfully managed complex programs in the past. We want to see your ability to oversee vendor activities and ensure compliance!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates during the process!

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 how you've successfully overseen vendor activities.

✨Showcase Your Project Management Skills

Prepare to highlight your project management skills during the interview. Think of instances where you managed complex programs, kept everything on track, and ensured compliance with quality standards. Use the STAR method (Situation, Task, Action, Result) to structure your responses.

✨Budget Savvy

Since managing external budgets is part of the role, be prepared to discuss your experience with budget oversight. Bring examples of how you've effectively managed budgets in previous roles, including any challenges you faced and how you overcame them.

✨Ask Insightful Questions

At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about their approach to data quality and compliance, or how they handle vendor relationships. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.

Global Clinical Data Manager - Submissions & Oversight in London
Cytel (EMEA)
Location: London
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  • Global Clinical Data Manager - Submissions & Oversight in London

    London
    Full-Time
    48000 - 72000 £ / year (est.)
  • C

    Cytel (EMEA)

    50-100
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