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Senior Clinical Research Associate - Spain - FSP

España🌐 Remote💼 Full-time🗓 2026-06-17 → 2026-08-01

Core

Senior Clinical Research Associate responsible for independent site monitoring, study setup, oversight, and regulatory submissions for oncology studies.

Role type

Senior Clinical Research Associate (Oncology)

Builds

Clinical trial operations for top 10 pharmaceutical companies

Domain

Life Sciences / Oncology / Clinical Research

Deliverable

client delivery

Required skills

Independent site monitoring, study setup and oversight, study status reporting, regulatory submission preparation, ICH GCP compliance understanding, time management, attention to detail

Preferred skills

Oncology study experience

Technologies

None stated

Responsibilities

Set up and oversee clinical studies, complete study status reports, maintain study documentation, participate in protocol and consent document submissions for ethics/IRB approval, assist in regulatory submissions

Seniority

Senior, hands-on IC

Rewrite
## About the role Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do. Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people. **Parexel FSP** is looking for a **Senior Clinical Research Associate** in **Spain** to strengthen our clinical operations team. Work from home and with the flexibility you want. Our SMs have less travel and less workload to maintain work-life balance. We offer long-term projects, world-class technology and training tailored to your individual experience. As a SM, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact. ## Responsibilities - Set up and oversee a study - Complete study status reports - Maintain study documentation - Submit protocols and consent documents for ethics/IRB approval - Assist in the preparation of regulatory submissions ## Requirements - Bachelor's degree in a life science or related discipline - Minimum of 5 years' experience in independent site monitoring and at least 2 years in oncology - Understanding of ICH GCP Compliance - Excellent time management and social skills - Highly motivated with a phenomenal eye for detail - Ability to travel domestically and internationally approximately 65%-75% of working time. Expected travelling ~2-3 days/week - Current driver's license required ## Benefits - Premium salary - Attractive benefits - Medical care plan: Health, Dental & Vision - Life Assurance - Excellent work environment - Culture of teamwork and collaboration - People who motivate and face challenges together - Innovative technology - Excellent training Our people and their passion are very important to us as they are the key to our success. That's why we provide you with an open and friendly working environment where we empower people and provide them with opportunities to develop their careers in the long term. In addition, you will have the opportunity to develop within your role and take on more responsibility or develop your skill set within other related Parexel FSP departments. Send your updated resume to **[email protected]** for an immediate interview. #LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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