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Clinical Data Associate

RadNet
Cambridge, MA Remote Full Time
POSTED ON 7/7/2024 CLOSED ON 8/5/2024

What are the responsibilities and job description for the Clinical Data Associate position at RadNet?

Job Summary

The Clinical Data Scientist works with the data science team to collect clinical data for machine learning algorithm development, for clinical studies related to FDA submission, and for research and scientific communications purposes. Responsibilities involve working with clinical data scientists to conduct clinical studies, analyzing data, managing IRB-related regulatory documentation, and acting as a bridge between DeepHealth and external academic and clinical partners. This role includes data science and clinical data management components, requiring the ability to work independently, solve problems creatively and communicate effectively.

Essential Duties and Responsibilities

  • Collects, cleans and curates imaging data and clinical meta data.
  • Performs summary analyses of data and report results.
  • Performs data wrangling tasks for algorithm development and clinical reporting.
  • Helps maintain data integrity and security.
  • Documents and tracks patient and imaging data.
  • Schedules study tasks with clinicians and administrators.
  • Interacts with clinicians to facilitate data collection.
  • Tracks IRB documentation for clinical studies and academic partnerships.
  • Participates in meetings and projects, and complete other duties as assigned by management.

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

Requirements:

Minimum Qualifications, Education, and Experience

  • Ph. D degree required.
  • Excellent communications skills (both written and oral).
  • Excellent project organization and time management skills.
  • Codingproficiency in Python.
  • Strong statistical knowledge and analysis skills
  • Experience working with large real-world datasets.
  • Self-starter with ability to work independently.
  • History of independent accomplishments and overcoming challenges.
  • Experience working with clinicians, preferred.
  • Publications in peer-reviewed manuscripts, preferred.

Quality Standards

  • Communicates, cooperates, and consistently functions professionally and harmoniously with all levels of supervision, co-workers, patients, visitors, and vendors.
  • Demonstrates initiative, personal awareness, professionalism and integrity, and exercise confidentiality in all areas of performance.
  • Follows all local, state and federal laws concerning employment to include but not limited to: I-9, Harassment, EEOC, Civil rights and ADA.
  • Follows OSHA regulations, RadNet and site protocols, policies and procedures.
  • Follows HIPAA, compliance, privacy, 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 and lunch schedules, and maintains satisfactory personal attendance in accordance with RadNet guidelines.
  • Consistently adheres to the time management policies and procedures.
  • Completes job responsibilities in a quality and timely manner.
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