Clinical Data Analyst II

RadNet • Somerville, MA

6d • Hybrid

About The Position

The Senior Clinical Data Analyst independently executes assigned clinical studies activities, applying comprehensive scientific knowledge to clinical data collection, management, quality assessment, analysis support, and documentation. This fully qualified professional-level position independently manages complex clinical imaging datasets, develops and optimizes data collection and processing workflows ensuring data integrity and process efficiency.

Essential Duties and Responsibilities
Executes assigned components of clinical studies independently managing assigned activities from planning through completion.
Manages the collection, maintenance, and quality of medical imaging data and associated clinical information from multiple clinical sites, ensuring data integrity and completeness.
Develops and implements image collection procedures and protocols in accordance with SOPs, Good Clinical Practice (GCP), FDA regulations, HIPAA, and other applicable requirements.
Collaborates with radiologists and cross-functional teams to establish and maintain ground truth standards for clinical imaging studies.
Assesses image data for quality and protocol compliance, resolves discrepancies, and maintains accurate image databases and tracking systems.
Support data analysis and contributes to interpretation of study results
Develops study documentation, technical reports, and scientific materials independently
Builds productive working relationships with internal teams and collaborates cross-functionally
Provides regular status updates on data collection activities and identifies opportunities to improve data collection, processing, and operational workflows.
Ensures compliance with regulatory, data privacy, and ethical standards
Works independently on assigned problems, applying sound scientific judgment and evaluation
PLEASE NOTE: This is not an exhaustive list of all duties, responsibilities and requirements of the position described above. Other functions may be assigned and management retains the right to add or change duties at any time.

Requirements

• BS degree and a minimum of 5 years of related experience; or a Master’s degree and 3 years of experience; or equivalent work experience
• Knowledge of clinical research principles and data analysis
• Proficiency in scientific computing, data analysis tools, and programming
• Strong attention to detail, documentation and communication skills
• Understanding of statistical methods and their application
• Experience working with real-world healthcare data, preferably imaging (dicom) data
• Demonstrated ability to work independently and manage assigned tasks to completion
• Communicates, cooperates, and consistently functions professionally and harmoniously with all levels of supervision, co-workers, visitors, and vendors.
• Demonstrates initiative, personal awareness, professionalism and integrity, and exercises confidentiality in all areas of performance.
• Follows all local, regional and country laws concerning employment.
• Follows all DeepHealth policies and procedures.
• Follows data privacy, compliance, safety and confidentiality standards at all times.
• Practices universal safety precautions.
• Promotes good public relations on the phone and in person.
• Adapts and is willing to learn new tasks, methods, and systems.
• Reports to work regularly as scheduled; consistently punctual with respect to working hours, meal and rest breaks, and maintains satisfactory personal attendance in accordance with DeepHealth guidelines.
• Completes job responsibilities in a quality and timely manner.

Responsibilities

• Executes assigned components of clinical studies independently managing assigned activities from planning through completion.
• Manages the collection, maintenance, and quality of medical imaging data and associated clinical information from multiple clinical sites, ensuring data integrity and completeness.
• Develops and implements image collection procedures and protocols in accordance with SOPs, Good Clinical Practice (GCP), FDA regulations, HIPAA, and other applicable requirements.
• Collaborates with radiologists and cross-functional teams to establish and maintain ground truth standards for clinical imaging studies.
• Assesses image data for quality and protocol compliance, resolves discrepancies, and maintains accurate image databases and tracking systems.
• Support data analysis and contributes to interpretation of study results
• Develops study documentation, technical reports, and scientific materials independently
• Builds productive working relationships with internal teams and collaborates cross-functionally
• Provides regular status updates on data collection activities and identifies opportunities to improve data collection, processing, and operational workflows.
• Ensures compliance with regulatory, data privacy, and ethical standards
• Works independently on assigned problems, applying sound scientific judgment and evaluation

What This Job Offers

• Job Type: Full-time
• Career Level: Senior