General Information

Location: Fremont, CA, Los Angeles, CA

Organization: Medavante-Prophase, Inc

Job Type: Part Time - Regular

Description and Requirements

The Principal Clinician IR/IRev will evaluate a wide range of psychiatric and cognitively impaired patients using several diagnostic and symptom rating scales as well as reviewing and providing feedback to site raters regarding their administration and scoring of standardized, structured interviews.


To be considered for U.S.-based positions unless currently employed by WCG, where permitted by applicable law (including any applicable reasonable accommodation, medical or religious exemption), candidates must have received or be willing to receive the COVID-19 vaccine by start date. 

 • Master’s degree conferred by a clinically-focused program in a mental health discipline such as Psychology, Social Work, Counseling, or Psychiatric Nursing. 


• Minimum of 2 years’ clinical experience diagnosing and/or treating patients with psychiatric     disorders, neurocognition disorders, and/or other study relevant indications. 
• Ability to conduct reviews of rater severity and/or diagnostic sessions, providing feedback for   quality control purposes.
• Proficiency with MS Word, Excel, Outlook, and PowerPoint. • Knowledge of GCP guidelines. 
• Bilingual (English/Spanish) communication skills, oral and written. 


  • Evaluate a patient’s current clinical condition and symptom severity. 
  • Perform diagnostic assessments. 
  • May also review, score, and provide feedback to site raters regarding the administration of standardized structured and semi-structured diagnostic and severity assessments as needed.
  • Conduct trainings for site raters.
  • Provide scoring for site assessments and/or review site scores.
  • Review site assessments for quality assurance.
  • Submit accurate data utilizing Good Clinical Practices and identified scoring conventions. 
  • Utilize technology required to conduct remote assessments. 
  • Follow Sponsor (protocol-specific) requirements and applicable MedAvante internal SOPs. 
  • Work with MedAvante Project Associates in initiating assessments and assist them with data query completion and data clarification.
  • Participate in Clinical meetings. 
  • Participate in on-going Clinician calibration and scoring exercises. 
  • May assume responsibility for major research and other projects. 
  • Responsible for keeping up to date with departmental and company communications to ensure one follows current policies, scale conventions, study procedures, and other pertinent information.


• Occasional travel may be required.