# Clinical Research Associate / Sr. Clinical Research Associate at Novartis

Novartis is hiring a Clinical Research Associate / Sr. Clinical Research Associate. It pays €36k-€67k a year and Level rates it Little AI ●○○○; you can [apply on Novartis](https://jobsbylevel.com/go/1ebe50f5-8cfb-4b86-908d-2d45381a6845?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. Madrid Provincial.

## Details

- Company: [Novartis](https://jobsbylevel.com/companies/novartis)
- AI level: AI Level 1 (score 37 out of 100)
- Location: Madrid Provincial
- Salary: €36k-€67k
- Posted: October 29, 2026
- Apply: https://jobsbylevel.com/go/1ebe50f5-8cfb-4b86-908d-2d45381a6845?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=clinical-research-associate-sr-clinical-research-associate-at-novartis-70b22f

## Description

Salary Range: €36,100.00 - €67,100.00 Job Description Summary Job Title: CRA / Sr CRA (Dual Posting) #LI-Hybrid Location: Madrid Provincial, Spain Relocation Support: This role is based in Madrid Provincial, Spain. Novartis is unable to offer relocation support: please only apply if accessible. Step into a role where your work directly advances clinical innovation and brings life-changing therapies closer to patients. As a Clinical Research Associate / Sr. Clinical Research Associate, you will be at the forefront of trial delivery—building trusted site partnerships, ensuring high-quality execution, and driving performance across Phase I–IV studies. In this site-facing role, you will take ownership of monitoring activities, proactively identify risks, and collaborate closely with cross-functional teams to ensure trials are delivered with excellence, integrity, and impact. Job Description Key Responsibilities Serve as primary point of contact between Novartis and clinical trial sites, ensuring strong, collaborative partnerships Manage assigned Phase I–IV study sites in compliance with protocols, monitoring plans, and regulatory requirements Conduct site initiation visits to ensure site teams are fully trained on study protocols and expectations Deliver ongoing training for amendments and new site personnel to maintain compliance and consistency Perform on-site and remote monitoring activities to ensure patient safety, data integrity, and protocol adherence Proactively assessing site performance, identifying risks and implementing mitigation strategies to improve outcomes Identify process gaps and collaborate with sites to drive continuous improvement and operational excellence Promote a strong compliance culture, ensuring adherence to ethical standards, regulations, and data privacy requirements Build strong site relationships to enhance patient recruitment and reduce operational challenges Lead site closeout activities, ensuring completion of follow-up actions and proper documentation and archiving Essential Requirements This is a dual posting for a CRA / Sr CRA. The final level and title offered will be determined by the hiring team based on the candidate's skills, experience, and capabilities for the level offered. Bachelor’s degree in a scientific or healthcare-related discipline. CRA: Minimum 1.5 years of experience in clinical research, including monitoring or site management; Sr CRA: Minimum 3 years of experience in clinical research, including monitoring or site management. Understanding of clinical trial processes, including Good Clinical Practice and International Council for Harmonization guidelines. Knowledge of applicable regulatory requirements and standards, including global and local health authorities. Strong communication and relationship-building skills to effectively collaborate with clinical trial sites. Ability to manage multiple priorities, demonstrating strong organization and time management skills. Analytical and risk-based thinking with the ability to identify issues and implement effective mitigation strategies. Fluency in written and spoken English and the local language. Desirable Requirements Strong understanding of the drug development process and clinical research methodologies. Benefits & Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: € 36,100 to € 67,100 The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/clinical-research-associate-sr-clinical-research-associate-at-novartis-70b22f

Source: https://jobsbylevel.com/jobs/clinical-research-associate-sr-clinical-research-associate-at-novartis-70b22f

## Cite this page

Level. https://jobsbylevel.com/jobs/clinical-research-associate-sr-clinical-research-associate-at-novartis-70b22f.

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