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Neuro Psychiatric Rater - United Kingdom/Travel in UK, Belfast
Client:
IQVIA
Location:
Belfast, United Kingdom
Job Category:
Other
EU work permit required:
Yes
Job Reference:
07a597cabd31
Job Views:
96
Posted:
22.01.2025
Expiry Date:
08.03.2025
Job Description:
PURPOSE
Responsible for administering clinical study assessments on a study. Observes the study participant’s symptoms and documents observations appropriately via psychiatric rating scales in accordance with study-specific requirements. Follows individual study participants through the study lifecycle and maintains documentation of observations for reporting purposes.
RESPONSIBILITIES
1. Administer clinical rating scales to support the diagnosis and assessment of symptom severity of subjects participating in CNS clinical studies.
2. Attend, complete, and qualify for study-specific rater training and certification for trials on which they rate.
3. Measure the severity of symptoms of study participants.
4. Continuously observe the study participants using approved assessments throughout the study.
5. Report to and work under the guidance of the principal investigator and/or sub-investigator for the study site where the study participant is seen.
6. Assist team in management and assessment of adverse events.
7. Support PI/Sub-I and study coordinators with assessments, data clarification, and data query completion.
8. Serve as Sub-I where applicable under the delegation of the PI.
EDUCATION AND EXPERIENCE
1. Medical Degree - Board certified psychiatrist PhD, MD or DO
2. Minimum two years of clinical experience and research experience with neuropsychiatric population.
3. Minimum two years of neuro psychiatric rater experience preferably, supporting clinical trials with > 25 assessments in the last year preferable.
4. Competency in rating scales as required by studies. Experience in specific scales will be assessed as needed for specific projects. Raters will undergo study rater training as required for each project. Compliance with all in-study rater training obligations and certification processes through trial duration.
ADDITIONAL ATTRIBUTES
1. Functional knowledge of ICH/GCP guidelines.
2. Functional knowledge of HIPAA and its application to clinical research.
3. Excellent oral and written communication skills.
4. Ability to function independently.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
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