ob Responsibilities:

Background and Responsibilities may include the following and other duties may be assigned:

• Participant Assessment: Conduct standardized assessments and evaluations of study participants according to study protocols and assessment manuals. This may involve administering structured interviews, questionnaires, and clinical rating scales to assess various domains such as pain severity, functional impairment, and quality of life.
• Data Collection: Collect and record accurate and reliable data during participant assessments, ensuring adherence to study procedures and protocols. Maintain detailed and organized records of assessment results and participant responses using electronic data capture systems or paper-based forms as required.
• Inter-Rater Reliability: Participate in inter-rater reliability exercises to ensure consistency and reliability in assessment procedures across multiple raters. Attend training sessions and calibration meetings to standardize assessment techniques and enhance reliability among raters.
• Adherence to Study Protocols: Follow study protocols, standard operating procedures (SOPs), and regulatory guidelines (e.g., Good Clinical Practice) in all aspects of participant assessment and data collection. Report any deviations from protocols or adverse events promptly to the study coordinator or principal investigator.
• Quality Assurance: Assist with quality assurance activities, including data monitoring, source document verification, and resolution of data queries and discrepancies. Review assessment forms and data entries for completeness, accuracy, and compliance with study requirements.
• Communication and Collaboration: Maintain open communication with study coordinators, principal investigators, and other team members to ensure smooth coordination of study activities. Collaborate with colleagues to address any issues or concerns related to participant assessment and data collection.