Clinical Research Associate Job at Syneos Health, Apply Now!
Are you passionate about clinical research and eager to make a difference in patients’ lives? Syneos Health is hiring a CRA I (Clinical Research Associate I) for our Functional Service Provider (FSP) model in Madrid, Spain. Join a globally respected CRO that supports 94% of all FDA-approved novel drugs, and be part of studies that transform lives. This is your chance to step into a role that blends meaningful impact, continuous learning, and professional growth in clinical development.
- Job Position: Clinical Research Associate I (CRA I) – FSP Model
- Location: Madrid, Spain
- Job ID: 25100032
- Employment Type: Full-Time
About The Company
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies because we are passionate to change lives.
Job Description
As a CRA I, you will be responsible for the effective on-site and remote monitoring of clinical trials. You will ensure compliance with study protocols, regulatory requirements, and industry best practices, while fostering communication between clinical sites and the study team. This role supports critical programs that bring innovative therapies to patients faster.
Key Responsibilities
- Conduct remote and on-site monitoring visits across clinical research sites in Spain
- Ensure data quality, protocol adherence, GCP compliance, and timely reporting
- Collaborate with clinical study teams to resolve site issues and monitor patient safety data
- Develop and implement SOPs, tools, and monitoring processes
- Maintain accurate documentation of visit findings, follow-up actions, and trial milestones
- Provide guidance to junior monitors as needed
- Ensure up-to-date knowledge of clinical research standards and regulatory changes
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related discipline
- 2–4 years of clinical research or pharmaceutical industry experience
- Working knowledge of ICH-GCP and clinical trial lifecycle
- Proficient with CTMS and EDC systems
- Strong verbal and written communication skills in English and Spanish
- Willingness to travel for site visits
Preferred:
- CRA certifications (CCRA, CCRP)
- Experience in the FSP model or global/multisite trial operations
Why Join Syneos Health?
- Global exposure with 29,000+ employees in 110 countries
- Inclusive Total Self culture that supports authenticity, wellbeing, and career development
- Involved in 200+ global studies impacting over 675,000 trial patients
- Access to continuous training, recognition programs, and robust career progression
Keywords: Syneos Health, Clinical Research, Job Opportunity, Monitoring, Pharmaceutical Industry, Madrid. Clinical Research Associate Job at Syneos Health, Apply Now!
