Clinical Research Associate II

Precision Medicine Group; Madrid; Híbrido; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

Precision Medicine Group is looking for a Clinical Research Associate II to be based in Madrid or Barcelona. The role involves monitoring clinical studies, ensuring compliance with protocols, and coordinating study activities. Candidates should have a 4-year degree, with at least 2 years of CRA experience, preferably in oncology.

Fluency in English and the local language is essential, along with a detail-oriented mindset. The position offers a balanced work environment with reasonable travel expectations.

Formación

• Minimum 2 years as a CRA in a CRO or pharmaceutical industry.
• Oncology monitoring experience preferred.
• Fluent in English and local language.

Responsabilidades

• Monitor and ensure clinical studies are conducted according to protocols.
• Coordinate activities for study setup and monitoring.
• Identify study risks and propose solutions.

Conocimientos

Monitoring clinical studies

Site management

Detail-oriented

Conflict resolution

Educación

4-year college degree or equivalent experience

Graduate or postgraduate degree in scientific or healthcare discipline

Descripción del empleo

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

Clinical Research Associate II – Madrid or Barcelona

We are looking for a Clinical Research Associate II based in Madrid or Barcelona.

Where You Fit In

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well‑prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose solutions on how to mitigate them.
• You take responsibility for the quality and outcomes of your work.
• You are adept at handling conflict by using tried and true resolution strategies.

Key Responsibilities

Monitor and own the progress of clinical studies at investigative sites and ensure that studies are conducted, recorded, and reported per protocol, SOPs, ICH‑GCP, and all applicable regulations and standards.

Coordinate all necessary activities required to set up and monitor a study (e.g., identify investigators; help prepare regulatory submissions; conduct pre‑study and initiation visits, etc.).

Minimum Requirements

• 4‑year college degree or equivalent experience.
• 2 (two) or more years as a CRA in a CRO or pharmaceutical/biotech industry, or equivalent experience.
• Site management or equivalent experience in clinical research.
• Oncology monitoring experience.

Other Required Criteria

• Availability for domestic travel including overnight stays, which may constitute up to 50‑60% travel commitment.
• Fluency in English and, for non‑English speaking countries, fluency in the local language of the country where the position is based.
• Candidates must reside in Madrid or Barcelona.

Preferred Qualifications

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline.

Equal Opportunity Employment

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.