Clinical Trial Associate

🔥 12 hours ago

🍂 Massachusetts – Remote

infoinfo

💵 $63.8k - $97.8k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🦅 H1B Visa Sponsor

infoinfo

👻 Ghost score 1%

infoinfo
Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

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

Logo of PathAI

PathAI

501 - 1000 employees

Founded 2016

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $165M Series C on 2021-05

Healthcare • Consulting • Logistics

PathAI is a leading healthcare technology company dedicated to advancing pathology through the use of artificial intelligence. Their mission is to improve patient outcomes by providing AI-powered technology that offers valuable insights for biomarker discovery and drug development. PathAI collaborates closely with biopharma and pathology laboratories to enhance laboratory workflows and improve diagnostics. Their AI-driven pathology solutions, such as the AISight Digital Pathology Image Management System, are utilized by major laboratories and research centers worldwide, helping to power digital pathology and precision medicine initiatives. PathAI's technology is leveraged by top biopharma companies to transform drug discovery and diagnostics, making significant contributions to the fields of healthcare and biotechnology.

📋 Description

• Monitor clinical trial lab services and engage with clinical investigator sites • Support the primary Clinical Trial Manager (CTM) • Apply knowledge of GCP, ICH, regulatory requirements, and Title 21 of the Code of Federal Regulations • Oversee timely closure of queries issued to investigator sites and designated parties • Identify trends and provide feedback on Investigator and PathAI BioPharma Laboratory performance • Monitor investigators, laboratory performance, study requirements, queries, pending results, and testing turnaround times • Collaborate with data management to resolve data discrepancies • Organize and track storage specimens, including receipt, retrieval, and shipping • Coordinate with external vendors and sponsors to deliver laboratory kits and test results • Perform routine study duties, including site lists, laboratory manuals, laboratory kit orders, specimen management reports, case assignments on the PathAI AISight CT Platform, and pending lab analysis • Support CTM administrative tasks, including action item tracking, meeting minutes, and process mapping • Provide backup CTM support, including client communication and study management • Collaborate with functional areas, vendors, Laboratory, Engineering, and support services • Coordinate site-level project information and escalate discrepancies • Assist with meeting and training materials • Support study start-up deliverables, milestones, project documentation, and close-out procedures • Perform other administrative or process-related duties as needed

🎯 Requirements

• 3+ years of clinical research experience in medical device and/or drug development clinical trials • BS or BA in a relevant scientific discipline • Good organizational skills • Attention to detail • Ability to multitask • Experience in digital pathology, radiology or other imaging technology-based clinical trials is highly preferred • Project Management Certification is a plus

🏖️ Benefits

• Remote work option • Relocation benefits are not available for this position

Apply Now

Similar Jobs

🕒 2 days ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Trial Associate supporting vendor spreadsheets and management during study start-up. Contributing to ICON’s sponsor-dedicated clinical research programs and treatment development.

🕒 2 days ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Trial Associate supporting study start-up vendor spreadsheets and management at ICON, a global clinical research organization. Coordinating study-team reporting and administrative processes.

🕒 September 18

QPS

51 - 200

🤝 B2B

☁️ SaaS

🏢 Enterprise

Clinical Trial Associate supporting QPS’s pharmaceutical, biotechnology, and medical-device research services. Coordinating study operations, documentation, meetings, compliance, budgets, and site activities.

🇺🇸 United States – Remote

💵 $60k - $75k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🚫👨‍🎓 No degree required

🕒 August 20

Karius

51 - 200

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Clinical Trial Associate supporting Karius’s genomic infectious-disease diagnostics through TMF and ISF documentation. Coordinating regulatory records, study meetings, milestones, audits, and clinical-site follow-up.