Clinical Research Associate

🔥 0 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 12%

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Medpace

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1992

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Medpace is a full-service contract research organization (CRO) that accelerates the development of safe and effective medical therapeutics. The company offers a comprehensive range of services to biopharmaceutical companies, including clinical trial management, regulatory affairs, and integrated laboratory services. With expertise across various therapeutic areas, Medpace facilitates collaboration among medical professionals to optimize the clinical development process and enhance trial efficiency.

📋 Description

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol • Communicate with medical site staff, including coordinators, clinical research physicians, and site staff • Verify investigator qualifications, training, resources, facilities, laboratories, equipment, and staff • Verify medical records and research source documentation against case report form data • Inform site staff of entry errors and ensure good documentation practices • Communicate protocol deviations according to SOPs, GCP, and applicable regulatory requirements • Verify that investigators enroll only eligible subjects • Review regulatory documents • Manage medical device and/or investigational product/drug accountability and inventory • Verify and review adverse events, serious adverse events, concomitant medications, and corresponding illnesses • Assess site patient recruitment and retention and offer improvement suggestions • Complete monitoring reports and follow-up letters, including summaries of findings, deviations, deficiencies, and recommended compliance actions

🎯 Requirements

• Minimum of a university degree in a health or life science related field • Minimum 1 year of experience as a Study Coordinator (SC), Clinical Research Coordinator (CRC), or CRA trainee • Approximately 60-80% travel • Proficient knowledge of Microsoft® Office and general computer literacy • Outstanding communication and presentation skills • Detail-oriented and efficient in time management • Excellent verbal and written communication skills in English and Spanish • Fluency in Catalan will be considered an asset • Application must be submitted in English

🏖️ Benefits

• Comprehensive initial and ongoing CRA training through the PACE Training Program • Defined CRA promotion and growth ladder with potential for mentoring and management advancements • Competitive pay • Opportunity for significant travel bonus • Office based environment with on-site mentors • Defined career paths with clear advancement opportunities • Industry renowned onboarding and training programs • Ongoing training and continuous learning opportunities • Comprehensive health, wellness, retirement, and PTO benefits • Office based culture with occasional WFH that provides flexibility for eligible positions after training • Company-sponsored social events

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