Mantell Associates is partnered with a reputable Pharmaceutical company, who is seeking a detail-oriented and proactive Clinical Research Associate (CRA) to join their clinical operations team. This role offers an opportunity to contribute to cutting-edge clinical trials across therapeutic areas, ensuring trial integrity, patient safety, and regulatory compliance across diverse European regions. Clinical Research Associate - Responsibilities:
Monitor clinical trial sites to ensure compliance with protocol, ICH-GCP, and local regulationsCoordinate study initiation, site training, site visits, and close-out activities as per trial timelines and deliverablesConduct source data verification (SDV), confirm data accuracy, and report deviations in collaboration with site and project leadsLiaise closely with clinical operations, data management, safety, and regulatory teams to address site issues, data queries, and safety reportingSupport site readiness, vendor oversight, and investigator communications with clear, compliant documentationProvide timely updates and reports on site status, performance metrics, and patient enrollment milestonesClinical Research Associate - Requirements:
1-3 years of experience in clinical monitoring, preferably within clinical research or development roles at a pharmaceutical company or CRO in the EUSound knowledge of ICH-GCP guidelines, EU clinical trial regulations (including CTR), and relevant national regulationsSolid academic background in Life Sciences, Pharmacy, Nursing, or a related disciplineStrong organisational skills, attention to detail, and ability to manage multiple sites or trials concurrentlyExcellent communicator in English; proficiency in additional European languages (e. g.
, German, French, Spanish) is a strong advantageBased in the EU, with travel flexibility to support European site visits and trial demandsMantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0)20 3854 7700.
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