Clinical Research Associate, All Levels

🔥 2 hours ago

🥔 Idaho, Montana, +2 more states – Remote

🥔 Idaho – Remote 🦬 Montana – Remote 🌲 Oregon – Remote ☕ Washington – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Performing all and any visit types while ensuring regulatory and protocol compliance • Participate in all aspects of a clinical trial from development and planning to study closure • Comply with applicable regulations, ICH/GCP and Evestia Clinical or sponsor SOPs to assess the safety and efficacy of investigational products (drugs, biologics or devices) • Maintain key performance metrics in accordance with company standards and timelines, ensuring compliance with established monitoring and reporting expectations • Ensure assigned sites are in compliance with the study protocol objectives • Work in project teams and under supervision, reporting to a Clinical Team Lead and/or Project Manager • Liaise effectively between sponsors, investigators and project teams • Completes all administrative tasks (expense and time reporting) within company guidelines • Perform any other duties as assigned

🎯 Requirements

• Substantial previous experience independently monitoring and performing all types of site visits • Ideally based in the South East • Understanding the principles of Good Clinical Practice (GCP) and clinical trial regulations • Both written and verbal communication and presentation skills • Understanding of medical terminology and human physiology • Proficiency with information technology (computer skills) • Excellent customer service skills • Demonstrated flexibility and adaptability • Ability to work in a team environment and independently as needed • Ability to travel nationally and internationally as required • Organizational and time management skills, able to prioritize tasks and work within timelines

🏖️ Benefits

• Health Insurance: 99% employer-paid • Dental & Vision Insurance: 100% employer-paid • Short-Term & Long-Term Disability: 100% employer-paid • Life Insurance Policy • 401(k) Retirement Plan: 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: Increases with tenure • Charitable Match Program • Wednesdays Catered Lunches (In-Office)