Clinical Research Associate I

Job not on LinkedIn

🔥 2 minutes ago

🏄 California, Washington – Remote

🏄 California – Remote ☕ Washington – Remote

💵 $90k - $110k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

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Evotec

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1993

🧬 Biotechnology

💊 Pharmaceuticals

🤖 Artificial Intelligence

Biotechnology • Pharmaceuticals • Artificial Intelligence

Evotec is a biotechnology company specializing in R&D and pipeline co-creation partnerships across various therapeutic and disease areas. The company leverages its AI-powered R&D platforms such as PanOmics and iPSC technologies to enhance disease understanding and human relevance. Evotec provides CRO/CDMO services, using cutting-edge continuous manufacturing technology and AI to improve access to high-quality biotherapeutics. Through its innovative business models, Evotec aims to deliver efficient and cost-effective solutions to unmet medical needs in collaboration with its partners.

📋 Description

• Assist with project management tasks within Clinical Development group • Collaborate with CRO(s) in the execution of clinical trials • Schedule meetings, set agendas, track action items and capture meeting minutes • Prepare, handle, distribute, file, and archive clinical documentation and reports • Monitor and QC the eTMF • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation • Coordinate and manage logistical aspects of clinical trials, such as shipment of lab samples • Help monitor the progress of clinical trials, track timelines and ensure adherence to protocol and other study documentation • Assist in the preparation of regulatory submissions • May review and approve invoices, purchase orders and site payments • Identify and address potential risks to the project timeline, quality, or budget and escalate when necessary • Help manage relationships with external vendors, including CROs, laboratories, and other service providers • Help ensure all study materials are properly archived following the completion of a trial

🎯 Requirements

• At least 3 years work experience as a Clinical Trial Assistant or CRA • Understanding of medical and pharmacological terminology • Knowledge of Good Clinical Practice (GCP) guidelines • Strong organizational and planning skills. • Project management experience a plus • Good communication and interpersonal skills • Experience working with CROs • Experience maintaining eTMF preferred • Proficient with MS Project and/or Smartsheet preferred • Experience managing clinical lab samples a plus • Data review experience plus BSc degree in life sciences or related field preferred

🏖️ Benefits

• Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow. • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life, with hybrid work schedules in many of our various locations. • Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged. • Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. • A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.