Clinical Research Associate

Job not on LinkedIn

🔥 1 hour ago

❄️ Minnesota – Remote

❄️ Minnesota – Remote

💵 $106k - $145.8k / year

⏰ Full Time

🟠 Senior

🔴 Lead

🧪 Clinical Research

👻 Ghost score 0%

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Solventum

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

📦 Logistics

💼 Consulting

Healthcare • Logistics • Consulting

Solventum is a healthcare-focused company renowned for its innovative solutions aimed at improving medical and oral care outcomes. The company offers a variety of medical technologies, including advanced wound care, surgical solutions, and sterilization products. Solventum also provides advanced oral care solutions, health information and technology services, and purification and filtration products for biopharmaceutical applications. Furthermore, Solventum places a strong emphasis on sustainability and education, providing resources and training for healthcare professionals globally. Their commitment to innovation and better healthcare has made them a leader in the healthcare industry, dedicated to enhancing patient safety and healthcare efficiencies.

📋 Description

• Prepare, collect, distribute, and maintain trial master file and regulatory documents at investigative sites • Conduct pre-study site visits and review site feasibility and operational processes • Prepare reports and participate in selecting investigators and study sites • Conduct clinical study site initiation visits and train site personnel on sponsor and regulatory requirements • Conduct site monitoring visits and follow up on significant problems and issues • Ensure clinical studies comply with state and federal regulations, guidelines, and policies • Review site files, records, case report forms, and source documents for completeness, accuracy, consistency, and compliance • Identify deficiencies and discrepancies and provide remedial training or initiate corrective action • Review and resolve case report form queries and data issues • Collaborate with the Clinical Project Manager, cross-functional study teams, and internal and external research partners • Assist with device preparation, shipment coordination, and accountability records

🎯 Requirements

• Bachelor’s degree or higher from an accredited institution and three (3) years of clinical research, biomedical, or medical device industry experience, including two (2) years of direct Clinical Research Associate (CRA) experience conducting clinical study monitoring activities; OR High School Diploma/GED and seven (7) years of relevant industry experience, including five (5) years of direct CRA experience conducting clinical study monitoring activities • Direct CRA monitoring experience with medical device clinical studies • Experience working in a hospital or clinical setting or medical laboratory • Experience using Smartsheet, Microsoft Copilot, and Microsoft 365 applications • Experience preparing and delivering verbal, written, and presentation communications regarding project status, issues, and escalations • Ability to identify problems, evaluate potential solutions, and support resolution of business or project issues • Ability to prioritize, plan, track, and evaluate deliverables against established requirements and timelines • Ability to manage multiple concurrent tasks and adjust priorities based on changing business needs and deadlines • Must be legally authorized to work in the country of employment without sponsorship for employment visa status

🏖️ Benefits

• Medical, Dental & Vision • Health Savings Accounts • Health Care & Dependent Care Flexible Spending Accounts • Disability Benefits • Life Insurance • Voluntary Benefits • Paid Absences • Retirement Benefits