46,800 €

Median Base Salary

How much does a Clinical Research Associate make in Madrid ?

The base salary for a Clinical Research Associate in Madrid is 46,800 €. Also known as: Clinical Research Scientist, Clinical Research Coordinator, Clinical Research Manager, Clinical Research Director, Clinical Research Technician, Clinical Research Fellow.
Access to more detailed salary information about the role with our salary platform

Start with 1 free search now
46,800 €

Median Base Salary (percentile 50th)

241 observations

Excellent Confidence

8,700 € Bonus per year

13,000 € of Stock

Base salary varies with experience. Register at TalentUp.io platform to learn about associated salaries based on seniority and percentiles. (Updated: Oct. 9, 2024)

Chart

26100 €

Min salary

61200 €

Max salary

Similar positions to

👤 Clinical Research Associate in 📍 Madrid

Salary Finder: Your Global Pay Guide 🚀

Search Salaries for Any Role, Anywhere in the World with our Salary Platform

Understand Your Role's Salary in-depth đź’ˇ

Get detailed information on seniority, bonuses, benefits, and pay growth. Register now to get crucial insights!

This is what our customers say about us đź’¬

Compensation transparency and fairness consulting

"I've found TalentUp to be an invaluable tool for salary benchmarking, especially when working with niche roles or unique geographical markets. The data they provide allows me to offer accurate and tailored compensation advice to my clients, complementing other sources. As a reward consultant, I always advise looking at multiple sources to build a full picture of the compensation landscape, and I'm confident to say that TalentUp is one of those sources!"

Avatar

Alistair Fraser

Founder | Justly

Sustainability in global supply chains collaboration

“TalentUp has been a game-changer for us. It provides clear insights that allow us to make well informed and fair compensation decisions. The intuitive interface and comprehensive overviews have become an integral part of our HR operations, ensuring efficiency and consistency across the board”.

Avatar

Alena Vititneva

Compensation and Benefits Manager | idh Trade

Global IT Selection Specialists

"We utilized this tool in assessment and consulting processes for a variety of positions, and the results were really useful. Having a tool that allows us to compare our experience—based on data and historical trends, as well as intuition and personal insights—provides us with great confidence in our recommendations, guaranteeing that we are presenting strong and well-founded solutions."

Avatar

Carles Font

CEO and Partner | Q-tech

Responsibilities: • Assisting in designing, planning, and implementing clinical research projects. • Conducting study start-up activities, including site selection and evaluation, and ensuring that sites are equipped with the necessary equipment and materials. • Monitoring the progress of clinical trials and ensuring that they are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements. • Assisting in the development and writing of clinical trial protocols, case report forms, and other study-related documents. • Managing data collection, organization, and review, ensuring data integrity and quality. • Liaising with investigators, site staff, and other professionals to ensure the smooth running of the trial. • Assisting in the preparation of reports and presentations of study results. Requirements: • Bachelor's degree in life sciences, nursing, or a related field. • Basic knowledge of clinical research process and medical terminology. • Understanding of Good Clinical Practice (GCP) and relevant regulatory guidelines. • Excellent organizational skills with the ability to manage multiple tasks. • Strong written and verbal communication skills. • Ability to work collaboratively as part of a team and independently with minimal supervision. • Detail-oriented with strong problem-solving skills. Preferred Skills: • Previous experience in a clinical research setting or similar role is preferred. • Proficiency in the use of various computer applications such as MS Office (Word, Excel, PowerPoint). • Strong interpersonal skills with the ability to effectively interact with all levels of staff and stakeholders. • Ability to interpret clinical data and statistical results. • Excellent time management skills with the ability to prioritize tasks effectively. • Ability to travel as necessary to monitor study sites. • Certification as a Clinical Research Associate or related certification is a plus.,

Explore Salary Insights in Detail

Gain comprehensive knowledge about seniority levels, bonuses, benefits, and salary growth trends.