Clinical Scientist/Senior Clinical Scientist/ Medical Data Reviewer/ Senior Medical Data Reviewer
Posted: 30 Jul 2024, 17:40
Job-Clinical Scientist/Senior Clinical Scientist/ Medical Data Reviewer/ Senior Medical Data Reviewer
Company: Parexel
Location: Hyderabad, Telangana, India
Job ID: R0000025123
Category: Medical Sciences
Key responsibilities:
Conduct comprehensive reviews of medical data in real-time, examining patient profiles and listings to detect any inconsistencies and assess medical plausibility at an individual level.
Engage in the analysis of trends at an aggregate level, providing medical, clinical, and scientific insights.
Examine investigational product dosing records for protocol adherence, identifying any potential inaccuracies or missed doses, and confirming protocol-specified actions for adverse events.
Verify all reported Adverse Events (AEs) for completeness and plausibility, ensuring all necessary information is present and accurate.
Assess all reported Concomitant Medications to confirm protocol compliance, relevance to existing medical conditions, or association with reported AEs.
Evaluate all laboratory results for completeness, adherence to the protocol's schedule, and identification of any potential safety concerns not reported in the AE data for the participant.
Provide administrative support as per the requirement.
Qualification: Bachelor of master’s degree in dental surgery, Physiotherapy, Nursing, M-Pharm/PharmD, BAMS, BHMS
Experience: 2-5 years’ experience in Medical data review or equivalent in clinical research
Click here to apply: https://jobs.parexel.com/en/job/hyderab ... 7608158128
Company: Parexel
Location: Hyderabad, Telangana, India
Job ID: R0000025123
Category: Medical Sciences
Key responsibilities:
Conduct comprehensive reviews of medical data in real-time, examining patient profiles and listings to detect any inconsistencies and assess medical plausibility at an individual level.
Engage in the analysis of trends at an aggregate level, providing medical, clinical, and scientific insights.
Examine investigational product dosing records for protocol adherence, identifying any potential inaccuracies or missed doses, and confirming protocol-specified actions for adverse events.
Verify all reported Adverse Events (AEs) for completeness and plausibility, ensuring all necessary information is present and accurate.
Assess all reported Concomitant Medications to confirm protocol compliance, relevance to existing medical conditions, or association with reported AEs.
Evaluate all laboratory results for completeness, adherence to the protocol's schedule, and identification of any potential safety concerns not reported in the AE data for the participant.
Provide administrative support as per the requirement.
Qualification: Bachelor of master’s degree in dental surgery, Physiotherapy, Nursing, M-Pharm/PharmD, BAMS, BHMS
Experience: 2-5 years’ experience in Medical data review or equivalent in clinical research
Click here to apply: https://jobs.parexel.com/en/job/hyderab ... 7608158128