CLINICAL RESEARCH ASSOCIATE (CRA), EU LANGUAGE-SPEAKING

CLINICAL RESEARCH ASSOCIATE (CRA), EU LANGUAGE-SPEAKING

CLINICAL RESEARCH ASSOCIATE (CRA), EU LANGUAGE-SPEAKING

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OXON Epidemiology, a leading growing mid-size international CRO specializing in real-world data, is seeking a proactive Clinical Research Associate (CRA) located in Spain to join our Madrid-based team . Prior experience in either a pharmaceutical company or a CRO environment is essential. Candidates must be fluent in English and have at least a B2 level in an EU language other than Spanish.

Send your CV and cover letter in English to , quoting the reference : 'EU language-speaking CRA. Only applications that provide these two elements will be considered.

Interviews with shortlisted candidates will be held in July 2025.

MAIN DUTIES AND RESPONSIBILITIES

As a Clinical Research Associate (CRA), you will be engaged in monitoring activities across all study phases, including site identification, site selection, study start-up, and regulatory and monitoring tasks for national and international observational studies (EU, US, Asia). Prior experience as a CRA, either in a pharmaceutical company or in a CRO (Clinical Research Organization) environment, is essential. Additionally, familiarity with ICH-GCP guidelines and international-local regulations is required. Fluency in both English and another EU language other than Spanish is essential.

Main tasks and responsibilities include :

Identify and select research sites.

Liaise with investigators on conducting the study.

Manage regulatory activities, including preparation of documentation and submission to competent health authorities and Ethics Committees (central and local).

Manage sites throughout the study duration, from site initiation visits to on-site monitoring visits or remote monitoring calls, data source verification, revision of CRFs, and site close-out visits.

Provide clinical and technical support for the project team as required.

Participate in departmental planning sessions.

Participate in internal meetings and occasionally external (with the Sponsor) conference calls and meetings to review the progress of ongoing studies.

Develop, prepare, attend, and take minutes for internal TCs.

Provide input to the development of study status reports for the Sponsor.

REQUIREMENTS :

Thorough knowledge of applicable clinical research regulatory requirements and clinical monitoring procedures.

Minimum of 2 years of independent monitoring.

Experience in a CRO or pharmaceutical setting.

Proficiency in MS SharePoint and other Microsoft Office products (Word, Excel, Outlook, PowerPoint, MS Project).

Experienced in regulatory submissions, contract negotiations, site management, and feasibility assessment.

Fluency in an EU language and English are essential requirements, as well as an ability to communicate effectively with others.

Ability to work to strict operational deadlines and manage conflicting priorities.

Excellent interpersonal and organizational skills, with the ability to collaborate effectively and manage multiple priorities within a matrix environment. Highly organized and detail oriented.

Ability to work independently, effectively prioritize tasks, and perform activities in a timely and accurate manner.

Proven ability to manage multiple projects simultaneously.

Be proactive and show initiative.

WE OFFER :

Full-time, permanent contract.

Flexible timetable and remote work options.

A competitive salary and benefits package.

Opportunities for professional development and growth.

Collaborative and inclusive work environment.

OXON EPIDEMIOLOGY is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive, friendly and learning environment for all employees. We encourage applications from candidates of all backgrounds and do not discriminate based on race, gender, age, religion, disability, sexual orientation, or any other protected status. Join us in building a diverse,talented and happy team!

COMPANY DESCRIPTION

OXON is a leading growing mid-size European-based full-service CRO providing global scientific and operational expertise in Real-World Evidence (RWE), RWE-driven Clinical Trials, and meta-analyses for drugs and devices across all major therapeutic areas, orphan diseases, pregnancy and vaccines. We maintain strong partnerships with the prestigious London School of Hygiene & Tropical Medicine and Oxford University and are a preferred provider for several top 20 pharmaceutical companies. With offices in London and Madrid, OXON leverages world-class expertise and innovative technologies to deliver high-quality (Lancet-worthy) real-world data, driven by a passion for advancing patient and public health.

For more information, visit

Seniority level

Seniority level

Entry level

Employment type

Employment type

Full-time

Job function

Job function

Research, Analyst, and Information Technology

Research Services

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