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For Companies At a Glance
- Tasks: Lead data management services for global clinical projects, ensuring accuracy and integrity.
- Company: Join a pioneering CRO dedicated to improving lives through innovative clinical trials.
- Benefits: Remote work, diverse teams, and opportunities for personal and professional growth.
- Why this job: Make a real impact in healthcare while collaborating with passionate professionals.
- Qualifications: Degree in Life Science or relevant experience; 5+ years in clinical data management.
- Other info: Inclusive environment that values creativity and collaboration.
The predicted salary is between 36000 - 60000 £ per year.
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Data Management department does at Worldwide
Our Data Management team is an ever-growing and collaborative group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies – from crafting the study database to ensuring the pristine delivery of the final dataset. We meticulously ensure data accuracy and integrity, crucial for groundbreaking regulatory submissions. With a variety of roles, from data support staff, database and SAS programmers, coders, and functional leads, there are many opportunities to launch and further your career. Our team embraces an environment that invites input, fosters personal growth, and empowers your professional journey.
What you will do
- Provide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programs.
- Ensure appropriate resources are allocated to complete all DM activities on time and budget.
- Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs).
- Write external vendor reconciliation specifications for programming reconciliation outputs (e.g. Serious Adverse Events, IRT, Central Laboratory).
- Monitor project scope, budgets and risks and alert DM Management of any concerns.
- Liaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings).
- Collaborate with internal Worldwide departments working on the same project.
- Participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings.
What you will bring to the role
- Excellent attention to detail with outstanding written and verbal communication skills.
- Strong knowledge of data management best practices & technologies as applied to clinical trials.
- Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
- Strong understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
- Strong analytical and problem solving skills.
- Independent and autonomous project oversight skills.
Your experience
- Educated to degree level (preferably Life Science), Nursing qualification, or relevant industry experience.
- Min of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
We love knowing that someone is going to have a better life because of the work we do.
Senior Clinical Data Manager - US/UK - Remote in North East employer: worldwide.com
Contact Detail:
worldwide.com Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Data Manager - US/UK - Remote in North East
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend virtual meetups, and engage on platforms like LinkedIn. 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 researching the company and its culture. Understand their mission and values, especially how they relate to improving lives. This will help you tailor your responses and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources to refine your answers. Focus on articulating your experience in clinical data management and how it aligns with the role at Worldwide Clinical Trials.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our innovative team at Worldwide.
We think you need these skills to ace Senior Clinical Data Manager - US/UK - Remote in North East
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Data Manager role. Highlight relevant experience in clinical data management and showcase your attention to detail. We want to see how your skills align with our mission!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about improving lives through clinical trials. Share specific examples of your past successes and how they relate to the role.
Showcase Your Communication Skills: Since communication is key in this role, make sure your application reflects your written and verbal skills. Keep your language clear and professional, and don’t forget to proofread for any typos!
Apply Through Our Website: We encourage you to apply directly through our careers page. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, you’ll get to explore other opportunities while you’re there!
How to prepare for a job interview at worldwide.com
✨Know Your Data Management Stuff
Make sure you brush up on your knowledge of data management best practices and technologies. Be ready to discuss how you've applied these in previous roles, especially in clinical trials. This will show that you’re not just familiar with the theory but have real-world experience.
✨Showcase Your Communication Skills
Since this role involves liaising with various teams and stakeholders, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated complex information in the past, whether it’s through written documentation or verbal presentations.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific challenges in data management. Think about past experiences where you had to solve problems or manage risks. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Demonstrate Your Leadership Qualities
As a Senior Clinical Data Manager, you'll need to show that you can lead projects independently. Prepare to discuss instances where you took charge, allocated resources, and ensured project timelines were met. Highlight your ability to motivate and guide team members as well.
