Senior Clinical Studies Associate

🔥 3 minutes ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $85k - $95k / year

⏰ Full Time

🟠 Senior

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

DeepHealth

WebsiteLinkedInAll Job Openings

11 - 50 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $225k Grant on 2019-08

Healthcare • Consulting • Logistics

DeepHealth is a global leader in AI-powered health informatics, providing innovative solutions designed to enhance operational efficiency and clinical confidence in radiology. As a wholly-owned subsidiary of RadNet, Inc. , DeepHealth offers a comprehensive suite of diagnostic and imaging tools, including the DeepHealth OS, a pioneering cloud-native operating system. Their AI-powered solutions support large-scale diagnostic programs and streamline workflows in areas such as breast, prostate, lung, and brain cancer detection. DeepHealth collaborates with leading healthcare institutions worldwide to transform radiology practices and improve care delivery.

📋 Description

• Supports the planning, execution, and oversight of clinical studies throughout the study lifecycle. • Contributes to study operations, documentation, regulatory compliance, and process improvement initiatives. • Develop study timelines, milestones, and project tracking tools. • Coordinate study meetings, prepare agenda, document meeting minutes, and track action items. • Facilitate communication among cross-functional teams, investigators, and stakeholders. • Identify and escalate routine study issues, risks, or delays as appropriate. • Draft, update, and maintain clinical study documentation. • Support the development, review, and completeness of study documents. • Conduct routine clinical data reviews and support data quality activities. • Prepare, coordinate, and track IRB submissions and related activities. • Support updates to SOPs, work instructions, templates, and operational tools as needed.

🎯 Requirements

• Bachelor’s degree in life sciences or related field (required); advanced degree preferred. • Minimum 2 years of related clinical research experience; or an advanced degree without experience; or equivalent work experience. • Working knowledge of Good Clinical Practice (GCP) and applicable regulatory guidelines. • Attention to detail and ability to manage multiple tasks concurrently. • Strong organizational and communication/collaboration skills. • Proficiency with clinical trial management systems and related tools.