Clinical Research Associate / Sr. Clinical Research Associate

ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.; Madrid; Hybrid; EUR 36,000 - 67,000; Full time

Benefits offered by this job

Hybrid working

Parental leave

Car allowance

Job summary

Novartis in Madrid Province is seeking a CRA/Senior CRA to monitor Phase I–IV trials, build strong site partnerships, and drive data integrity and patient safety. This dual posting emphasizes site-facing responsibilities and hybrid work options.

The role requires a Bachelor’s degree in a scientific or healthcare field, 1.5+ years (CRA) or 3+ years (Sr CRA) in clinical research, and fluency in English and Spanish. Competitive base salary €36,100–€67,100 plus benefits and potential bonus.

Qualifications

• Bachelor’s degree in a scientific or healthcare discipline.
• CRA: 1.5+ years of clinical research experience including monitoring or site management.
• Sr CRA: 3+ years of clinical research experience including monitoring or site management.

Responsibilities

• Serve as primary contact between Novartis and clinical trial sites.
• Manage Phase I–IV study sites in compliance with protocols and regulatory requirements.
• Conduct site initiation visits and ensure site teams are trained on study protocols.
• Deliver ongoing training for amendments and new site personnel.
• Perform on-site and remote monitoring to ensure patient safety and data integrity.

Skills

Monitoring

Site management

Communication

Risk assessment

English fluency

Education

Bachelor’s degree in scientific or healthcare field

Tools

CTMS

GCP/GxP knowledge

Job description

Job Description Summary

Salary Range: €36,100.00 - €67,100.00

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 PhaseI–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.

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

• 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 professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs.

In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable.

A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Skills Desired

• Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Collaboration, Data Integrity, Decision Making, Life Science

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.