Clinical Research Associate, All Levels

🔥 16 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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Evestia Clinical

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1996

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Evestia Clinical is a global specialist Contract Research Organization (CRO) that provides customized clinical development services to biotech innovators. Formed through the acquisition of EMAS Pharma by Kester Capital and a subsequent strategic merger with Atlantic Research Group (ARG), Evestia Clinical operates from headquarters in Letchworth, UK and Charlottesville, Virginia, USA. The combined team of over 150 professionals delivers tailored solutions across the full drug development lifecycle (Phase 1–3 and beyond), with particular expertise in oncology, neurology, rare diseases, immunology, and inflammation. The company emphasizes global trial infrastructure, regulatory support, integrated data and biostatistics platforms, and personalized, agile clinical research services for biotech clients.

📋 Description

• Perform site management and monitoring activities, including site qualification, initiation, interim monitoring, and close-out visits • Participate in clinical trials from development and planning through study closure • Ensure assigned clinical trial sites comply with study protocols, applicable regulations, ICH/GCP, and company or sponsor SOPs • Review source documentation and clinical data for accuracy, completeness, and consistency • Monitor participant safety, informed consent processes, investigational product accountability, and protocol compliance • Identify, document, escalate, and support resolution of issues, including protocol deviations and data queries • Maintain key performance metrics according to company standards, project requirements, and timelines • Prepare monitoring reports and required study documentation accurately and on time • Collaborate with Clinical Team Leads, Project Managers, sponsors, investigators, site personnel, and cross-functional teams • Build and maintain relationships with clinical research sites and study stakeholders • Complete administrative activities, including expense and time reporting • Provide mentoring, guidance, and subject matter support to less experienced team members when appropriate • Perform other assigned duties

🎯 Requirements

• Degree in life sciences, nursing, pharmacy, or a related field; equivalent education and clinical research experience may be considered • Previous experience in clinical research, clinical operations, healthcare, or a related field is preferred; experience requirements vary by level • Experienced CRA candidates require previous independent monitoring experience and ability to perform applicable site visit types • Working knowledge of Good Clinical Practice (GCP), clinical trial regulations, and research ethics • Understanding of medical terminology, human physiology, and clinical trial processes • Strong written, verbal, and presentation skills • Proficiency with information technology and clinical trial systems • Excellent customer service, communication, and relationship-building skills • Flexibility, adaptability, and attention to detail • Ability to work effectively in a team environment and independently as needed • Organizational and time management skills, with ability to prioritize tasks and meet project timelines • Ability to travel nationally and internationally as required • Ideally based on the West Coast or within reasonable access to West Coast clinical trial sites

🏖️ Benefits

• 99% employer-paid health insurance • 100% employer-paid dental and vision insurance • 100% employer-paid short-term and long-term disability • Life insurance policy • 401(k) retirement plan with 3% employer contribution • Flexible and hybrid work options • Unlimited PTO for salaried staff • 12 corporate holidays • Employee Assistance Program (EAP) • Wellness program • Learning & Development stipend that increases with tenure • Charitable Match Program • Wednesdays catered lunches (in-office)