Senior Clinical Research Associate

Precisionmedicinegroup·RemoteRemotesenior

In short

→Asociado Senior de Investigación Clínica que supervisa estudios en sitios, asegurando cumplimiento con protocolos y normas.
→Día a día: visitas a centros, coordinación de estudios, supervisión de calidad, formación de junior y trabajo directo con clientes.
→Destacado: Posibilidad de trabajo 100% remoto en Francia, con viajes del 50-60% y oportunidad de crecer en un entorno colaborativo.

Fluency in English is required

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What they ask for

✓Título universitario de 4 años o experiencia equivalente
✓Certificado de CRA
✓Mínimo 5 años de experiencia como CRA/SCRA en CRO, farmacéutica, biotecnología o dispositivos médicos
✓Experiencia en monitoreo de estudios en múltiples áreas terapéuticas
✓Disponibilidad para viajar domésticamente (50-60%), con estancias nocturnas
✓Fluidez en inglés y en el idioma local

Don't tick every box? That's normal — your free dossier shows your gaps and how to cover them in the interview.

protocolosSOPsICH-GCPnormas y regulaciones aplicablpreparación de presentacionespresentaciones a clientesactividades de inicio de estudgestión financieraformación y mentoría de personiniciación de pagos

Who should you write to at Precisionmedicinegroup?

Your free dossier identifies the people who'd interview you — their background, what they value, and how to reach out so you stand out before applying.

At Precision for Medicine, we are always looking to connect with exceptional talents, and we are currently seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to support a dedicated FSP partnership , working closely with a strategic sponsor in a highly collaborative and quality-focused environment. This evergreen posting is part of our ongoing talent pipeline strategy and enables interested candidates to be considered for future opportunities aligned with upcoming project requirements. While there may not be an immediate opening, candidates whose experience matches our anticipated needs will be considered for future opportunities as they arise. This position can be offered fully home-based within France. About you: • 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 in the quality and outcomes of your work. • You are adept at handling conflict by using tried and true resolution strategies. How we will keep you busy and support your growth: You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.). Senior CRAs handle appropriately sized clinical trials, and support clinical study teams with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations. Qualifications: Minimum Required : • 4-year college degree or equivalent experience • Holder of CRA certificate Other Required : • Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment • Experience monitoring clinical trials across a variety of therapeutic areas. • Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions) • Fluency in English and the local language is required • Additional language(s) will be considered an asset Preferred : • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline • Study start up activities experience • For Senior CRAs, understanding of financial management Why Precision for Medicine? At Precision for Medicine, we combine the agility and collaboration of a specialized CRO with the scientific expertise needed to support innovative clinical development programmes. Our employees are empowered to make an impact, build meaningful client relationships, and grow their careers in an environment that values quality, accountability, and professional development. Please note: This is an evergreen opportunity intended to build our network of experienced clinical research profess

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