At a Glance
- Tasks: Join us as a Centralized Monitoring Analyst, supporting clinical projects and ensuring data quality.
- Company: IQVIA is a global leader in clinical research and healthcare intelligence, dedicated to improving patient outcomes.
- Benefits: Enjoy remote work flexibility and the chance to collaborate with diverse teams across Europe and South Africa.
- Why this job: Be part of a mission-driven company that values innovation and contributes to global health improvements.
- Qualifications: 3+ years in pharmaceutical research and 2-3 years of SAS programming experience required.
- Other info: This role offers a unique opportunity to work directly with clients on impactful projects.
The predicted salary is between 36000 - 60000 £ per year.
This unique role within IQVIA is for a Lead Programmer on Cluepoints, called a Centralized Monitoring Analyst (CMA), requiring strong communication and organizational skills. Experience with SAS programming is necessary. The role can be based remotely in various European countries or South Africa. This position is part of a sponsor-dedicated project, working directly with the client to manage deliverables.
Main Responsibilities:
- Support the Centralized Monitoring Lead (CML) in developing a fit-for-purpose CM strategy, including identifying relevant CM elements such as QTLs, KRIs, data visualizations, and Data Quality Assessments.
- Set up and program QTLs, KRIs, and Data Quality Assessments according to the study's Centralized Monitoring Plan (CMP).
- Refresh the Centralized Monitoring Platform regularly to enable signal detection.
- Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF.
- Review and understand study protocols thoroughly.
- Understand data sources, transfer specifications, and data structure for the study.
- Perform peer-reviews of CM platform setups conducted by colleagues.
Experience and Skills:
- Minimum of 3 years relevant experience in pharmaceutical research, development, or related fields, preferably in centralized monitoring, data management, or biostatistics.
- 2-3 years of SAS experience, including macro language, is preferred.
- Ability to work autonomously and engage with stakeholders to execute centralized monitoring activities.
- Basic understanding of statistical analysis concepts and interpretation of outcomes.
- Ability to maintain data confidentiality.
- Self-motivated with minimal supervision.
- Strong communication, interpersonal, organizational, and problem-solving skills.
- High initiative, drive, and commitment.
- Prior experience in Data Management is required.
- Experience with relational databases, Clinical Data Management, and EDC Systems.
- Experience communicating across all organizational levels and working in collaborative teams globally.
- Knowledge of federal regulations, GCP, and Good Clinical Data Management Practices.
- Excellent command of English, both verbal and written.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We aim to accelerate the development and commercialization of medical treatments to improve patient outcomes worldwide. We value diverse talent with curious minds and a commitment to innovation. Everyone at IQVIA contributes to our mission of improving lives globally.
Clinical Monitoring Analyst (CMA) employer: Nanosep AB
Contact Detail:
Nanosep AB Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Monitoring Analyst (CMA)
✨Tip Number 1
Familiarise yourself with the specific tools and technologies mentioned in the job description, particularly SAS programming. Consider taking online courses or tutorials to enhance your skills, as this will demonstrate your commitment and readiness for the role.
✨Tip Number 2
Network with professionals in the clinical monitoring field, especially those who have experience with centralized monitoring. Engaging in relevant forums or LinkedIn groups can provide insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences in data management and how they relate to the responsibilities of a CMA. Be ready to share specific examples of how you've successfully managed data quality assessments or similar tasks.
✨Tip Number 4
Research IQVIA's recent projects and initiatives in clinical research. Being knowledgeable about their work will not only help you during interviews but also show your genuine interest in the company and its mission.
We think you need these skills to ace Clinical Monitoring Analyst (CMA)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Monitoring Analyst position. Familiarise yourself with key terms like QTLs, KRIs, and Data Quality Assessments to demonstrate your knowledge in your application.
Tailor Your CV: Customise your CV to highlight relevant experience in pharmaceutical research, SAS programming, and data management. Emphasise your skills in communication, organisation, and problem-solving, as these are crucial for the role.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for clinical research and your understanding of the Centralized Monitoring Analyst role. Mention specific experiences that align with the job description and how you can contribute to IQVIA's mission.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail and professionalism, which are essential in this field.
How to prepare for a job interview at Nanosep AB
✨Know Your SAS Inside Out
Since the role requires strong SAS programming skills, make sure you brush up on your knowledge of SAS, especially the macro language. Be prepared to discuss your previous projects and how you've used SAS to solve problems or improve processes.
✨Understand Centralized Monitoring Concepts
Familiarise yourself with key concepts like QTLs, KRIs, and Data Quality Assessments. Be ready to explain how these elements fit into a Centralized Monitoring Plan and provide examples from your past experience where applicable.
✨Demonstrate Strong Communication Skills
As this role involves working directly with clients and stakeholders, showcase your communication skills during the interview. Practice articulating complex ideas clearly and concisely, and be prepared to discuss how you've successfully collaborated with teams in the past.
✨Showcase Your Problem-Solving Abilities
The interviewer will likely want to see how you approach challenges. Prepare examples of past situations where you identified a problem, developed a solution, and implemented it effectively. Highlight your initiative and ability to work autonomously.