At a Glance
- Tasks: Review and evaluate clinical data for trials, ensuring accuracy and quality control.
- Company: Join Clario, part of Thermo Fisher Scientific, in a collaborative global environment.
- Benefits: Enjoy competitive pay, remote work options, and opportunities for professional growth.
- Other info: Dynamic role with a focus on teamwork and continuous improvement.
- Why this job: Make a real impact by supporting life-changing therapies through data management.
- Qualifications: Bachelor’s degree or relevant experience in data management or life sciences.
The predicted salary is between 30000 - 40000 € per year.
Clario, a part of Thermo Fisher Scientific, is seeking a Clinical Data Management Associate II to support the review and evaluation of clinical data generated from the imaging components of sponsor clinical trials across multiple therapeutic areas. This role is responsible for delivering accurate, timely, and consistent clinical data to internal teams and client organizations in support of project and business objectives. The Associate II helps define and execute data management workflows for assigned projects, ensuring appropriate data quality control measures are applied throughout the study lifecycle.
What We Offer- Competitive compensation and benefits
- The opportunity to work remotely within the United Kingdom
- A collaborative, global environment supporting professional growth and development
- Review project documentation and requirements for new studies and anticipate impacts to Data Management (DM) standards and processes
- Collaborate with cross‐functional project teams to stay informed of changes affecting data collection, cleaning, and data transfers
- Support study implementation and data collection activities in alignment with project requirements
- Define, run, and review edit checks; identify and resolve data discrepancies
- Maintain organized, complete, and current study documentation
- Create and/or review study Transmittal Forms, ensuring alignment with established standards
- Keep the supervisor informed of project status, risks, and milestones
- Review clinical data to identify errors and inconsistencies
- Develop study data specifications, including data transfer specifications, system configuration specifications, and data validation rules
- Partner with project teams to resolve data issues and track outstanding actions through to resolution
- Prepare and validate ad hoc data listings as required
- Ensure system bugs and enhancement needs are reported to the appropriate Product Manager and that any interim programming solutions are approved
- Adhere to departmental processes, standards, and applicable Standard Operating Procedures (SOPs)
- Participate in the review and updating of SOPs related to Data Management
- Collaborate with internal colleagues to resolve issues and support team objectives
- Contribute ideas to improve processes and add value to the organization
- Support team success by assisting others as needed
- Participate in relevant company‐sponsored training to maintain technical and industry knowledge
- Perform other duties as assigned
- Bachelor’s degree in Computer Science, Life Sciences, or a related field preferred, or equivalent relevant experience
- Approximately one year of experience in a comparable role within the pharmaceutical, biotechnology, or CRO industry
- Working knowledge of relational database organization and data validation principles
- Experience with office productivity tools such as Microsoft Word, Excel, and Access preferred
- Understanding of clinical trial terminology
- Demonstrated problem‐solving ability
- Ability to work independently while contributing effectively within a team environment
- Strong attention to detail and organizational skills
- Effective interpersonal and communication skills, both written and verbal
- Professional, positive approach with the ability to adapt to changing priorities
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you’re starting your clinical data career or building long‐term expertise, your work helps bring life‐changing therapies to patients faster.
Clinical Data Management Associate II employer: Clario Holdings Inc.
Clario, part of Thermo Fisher Scientific, is an exceptional employer that offers a competitive compensation package and the flexibility of remote work within the United Kingdom. Our collaborative and inclusive work culture fosters professional growth and development, empowering employees to contribute meaningfully to life-changing clinical trials while enjoying a supportive environment that values innovation and teamwork.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Data Management Associate II
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical data management field on LinkedIn. Join relevant groups and participate in discussions to get your name out there and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by practising common questions related to clinical data management. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers and showcase your problem-solving skills effectively.
✨Tip Number 3
Don’t just apply; follow up! After submitting your application through our website, send a polite email to express your enthusiasm for the role. It shows initiative and keeps you on their radar.
✨Tip Number 4
Stay updated on industry trends and advancements. Subscribe to relevant journals or blogs, and mention any new knowledge during interviews. It demonstrates your commitment to professional growth and understanding of the field.
We think you need these skills to ace Clinical Data Management Associate II
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Data Management Associate II role. Highlight relevant experience and skills that match the job description, like your knowledge of data validation principles and clinical trial terminology.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical data management and how your background makes you a great fit for our team at Clario. Keep it concise but impactful!
Showcase Your Attention to Detail:In this role, attention to detail is key. When filling out your application, double-check for any typos or errors. This not only reflects your skills but also shows us you care about quality.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and allows us to see your enthusiasm for joining our team!
How to prepare for a job interview at Clario Holdings Inc.
✨Know Your Data Management Basics
Before the interview, brush up on your knowledge of clinical data management principles and terminology. Be ready to discuss how you would handle data discrepancies and ensure data quality control measures are applied throughout the study lifecycle.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experiences where you successfully identified and resolved data issues. Highlight your analytical thinking and how you collaborated with teams to track outstanding actions through to resolution.
✨Familiarise Yourself with the Company
Research Clario and its role within Thermo Fisher Scientific. Understand their mission to transform lives through better evidence and be prepared to discuss how your values align with theirs during the interview.
✨Prepare Questions for Them
Think of insightful questions to ask your interviewers about the team dynamics, project workflows, and opportunities for professional growth. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.
