Clinical Trial Psych Rater - Chinese (Simplified, China)

extra holidays
Work set-up: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Master's degree in Psychology, Counseling, Psychiatric Nursing, or Social Work; MD, DO, or PhD preferred., At least 3 years of experience in psychiatric assessments, ratings scales, or structured clinical interviews., Minimum of 3 years of clinical experience with psychiatric populations., Proficiency in administering scales in clinical research trials and strong interpersonal skills..

Key responsibilities:

  • Review and evaluate assessment scales administered by raters to ensure standardization and data quality.
  • Conduct live interactions with raters to discuss assessment methodology and scoring techniques.
  • Participate in training, calibration, and documentation activities related to clinical assessments.
  • Assist in preparing and disseminating communications related to clinical trial assessments.

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Job description

Clinical Specialist Consultant - Chinese Speaking (Simplified, China)

 

Location:  Remote/virtual

Hours:  Estimated 10-16h/month

Role:  Clinical Specialist

 

Job Description:

The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is evaluated, and live interaction with raters is conducted to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Other Clinical Specialist responsibilities may include, but are not limited to, functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.

 

Required Experience, Knowledge, Skills:

• Minimum of a master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing or Social Work, or equivalent.  MD, DO or PhD preferred

Minimum of 3 years’ experience administering psychiatric assessments, ratings scales and/or structured clinical interviews.  Specifically, EQ-5D-5L (Interviewer administered and Proxy 1 version) & mRS.

• Minimum of 3 years clinical experience with related psychiatric populations.

• Minimum of 3 years' experience with administering scales in clinical research trials (not including graduate/doctoral research work).

• Experience in central nervous system (CNS) trials preferred.

• Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.

• Excellent organization, attention to detail, time management and problem-solving skills.

• Computer proficiency with Windows and Microsoft Office system and applications.

 

Tasks/Responsibilities:

• Participate in all orientation, training and calibration activities as required.

• Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).

• Complete rater interactions and assigned tasks as scheduled.

• Responsible for timely submission of all documentation associated with assigned tasks.

 

*Current openings require fluency in English and a native speaker in the language needed for the trial.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Social Skills
  • Microsoft Office
  • Computer Literacy
  • Time Management
  • Detail Oriented
  • Problem Solving

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