At a Glance
- Tasks: Support Centralized Monitoring processes and manage client deliveries with strong programming skills.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Work autonomously in a dynamic environment with global collaboration opportunities.
- Why this job: Make a real impact in healthcare by improving patient outcomes through innovative monitoring strategies.
- Qualifications: 3+ years in pharmaceutical research, SAS programming experience, and strong communication skills.
The predicted salary is between 40000 - 50000 € per year.
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries.
The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP).
Main Responsibilities- Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments)
- Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP
- Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification
- Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF
- Review and understanding of protocol is key
- Understand the data sources for the study, the data transfer specifications and the data structure
- Execute and document peer-review of CM platform setup done by other CMA colleagues
- At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics
- 2-3 years SAS experience including macro language
- Knowledge/ experience working on Cluepoints
- Ability to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process.
- Ability to understand basic statistical analysis concepts and to interpret their outcome.
- Ability to maintain confidentiality of data and information during interactions with staff at all levels
- Ability to work with limited close supervision.
- Demonstrated communication, interpersonal, organizational and problem-solving skills
- High levels of initiative, drive and commitment.
- Prior experience in a Data Management related field is required
- Experience with relational databases, preferably Clinical Data Management and EDC Systems
- Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally).
- Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.
- Excellent command, both verbal and written, of English
This role is not eligible for UK visa sponsorship.
Clinical Monitoring Analyst (Cluepoints) - Remote in Reading employer: IQVIA Laboratories
IQVIA is an exceptional employer that fosters a collaborative and innovative work culture, particularly for the Clinical Monitoring Analyst role. With a strong emphasis on employee growth and development, team members are encouraged to enhance their skills in a supportive environment while working remotely. The company offers competitive benefits and the unique opportunity to engage directly with clients, making a meaningful impact in the life sciences and healthcare industries.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Monitoring Analyst (Cluepoints) - Remote in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at IQVIA or have experience with Cluepoints. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for the interview by brushing up on your SAS programming skills and understanding the Centralized Monitoring process. We want you to be able to discuss your experience confidently and show how you can contribute to the team.
✨Tip Number 3
Showcase your communication and organisational skills during the interview. Be ready to share examples of how you've successfully managed projects or collaborated with stakeholders in the past. This is key for the Clinical Monitoring Analyst role!
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're serious about joining the team at IQVIA.
We think you need these skills to ace Clinical Monitoring Analyst (Cluepoints) - Remote in Reading
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Monitoring Analyst role. Highlight your SAS programming experience and any relevant projects you've worked on. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background in pharmaceutical research aligns with our needs. Keep it engaging and personal – we love to see your personality!
Showcase Your Communication Skills:Since strong communication is key for this role, make sure to demonstrate your ability to convey complex information clearly in your application. Whether it's through your CV or cover letter, let us see how you can connect with stakeholders effectively.
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. Plus, it shows us that you're serious about joining our team at StudySmarter!
How to prepare for a job interview at IQVIA Laboratories
✨Know Your SAS Inside Out
Since this role requires at least 2-3 years of SAS experience, make sure you brush up on your SAS programming skills. Be prepared to discuss specific projects where you've used SAS, especially in relation to Centralized Monitoring or data management.
✨Understand the Centralized Monitoring Process
Familiarise yourself with the Centralized Monitoring process and the key elements like Quality Tolerance Limits (QTL) and Key Risk Indicators (KRI). Being able to explain how these concepts apply to the role will show that you're not just a fit for the job, but also genuinely interested in it.
✨Communicate Clearly and Confidently
Strong communication skills are essential for this position. Practice articulating your thoughts clearly, especially when discussing complex topics like data visualisations or statistical analysis. Remember, it's not just about what you say, but how you say it!
✨Showcase Your Problem-Solving Skills
Prepare examples of past challenges you've faced in data management or clinical research and how you overcame them. This will demonstrate your initiative and problem-solving abilities, which are crucial for working autonomously in this role.
