Job Title: Clinical Specialist / Stroke Rater – Bengali Speaking
Location: Chennai, India (Home-Based / Remote)
Employment Type: Part-Time
Estimated Hours: 2–12 Hours per Month (Flexible Schedule)
Reference ID: R1524563
Industry: Clinical Research | Neurology | Stroke Trials | CRO
IQVIA is seeking a qualified Clinical Specialist / Stroke Rater (Bengali Speaking) to support ongoing stroke clinical trials. This part-time, home-based opportunity is ideal for healthcare professionals with experience in stroke patient assessment, neurological rating scales, and clinical trial protocol compliance.
As a global leader in clinical research and healthcare intelligence, IQVIA partners with pharmaceutical, biotechnology, and medical device companies to ensure high-quality data collection and standardized outcome assessments in neurological studies.
The Clinical Specialist will support stroke-focused clinical trials by administering standardized stroke rating scales and reviewing assessments conducted by other raters. This role ensures data accuracy, protocol adherence, and inter-rater reliability across study sites.
The position requires fluency in Bengali and the ability to conduct remote patient and rater interactions professionally and consistently.
Administer validated stroke rating scales to trial participants, including:
EQ-5D-5L (Interviewer and Proxy Versions)
Modified Rankin Scale (mRS)
Ensure accurate and consistent scoring aligned with clinical trial protocols.
Maintain certification and calibration standards for stroke assessments.
Review stroke assessments performed by other raters to ensure protocol compliance.
Evaluate scoring accuracy and methodological consistency.
Conduct live feedback sessions with raters to support scoring improvements and standardization.
Participate in mock interviews and functional rater performance assessments.
Review case documentation prior to rater discussions.
Complete required documentation and reporting within defined timelines.
Participate in ongoing training, orientation, and calibration sessions.
Ensure adherence to study protocols and regulatory requirements.
Minimum 1 year of clinical experience managing or assessing stroke patients.
Prior experience administering stroke-related rating scales within clinical trials.
Demonstrated experience in neurological assessments and structured outcome evaluations.
Familiarity with inter-rater reliability standards in multicenter trials is preferred.
Minimum: Master’s degree (MA/MS) in Medicine, Neurology, Psychology, or related healthcare field.
Preferred: MD, DO, or PhD.
Equivalent advanced clinical qualifications with stroke expertise may be considered.
Proven proficiency in:
EQ-5D-5L administration
Modified Rankin Scale (mRS) scoring
Strong understanding of stroke clinical trial protocols.
Excellent interpersonal and professional communication skills.
Strong organizational skills and attention to detail.
Ability to manage flexible part-time commitments (2–12 hours per month).
Fluency in Bengali (mandatory).
Comfort working remotely in a home-based clinical research environment.
Fully remote / home-based role.
Flexible monthly workload (estimated 2–12 hours).
Interaction with global clinical trial teams.
Contribution to high-impact neurological and stroke research programs.
This role provides:
Exposure to international stroke clinical trials.
Opportunities to enhance expertise in neurological outcome assessments.
Involvement in quality assurance and inter-rater reliability processes.
Flexibility suitable for practicing clinicians seeking part-time research engagement.
IQVIA is a global leader in clinical research services, advanced analytics, and healthcare intelligence. The organization supports life sciences innovation by combining scientific expertise with technology-driven data solutions to accelerate drug development and improve patient outcomes worldwide.
If you have at least 1 year of stroke clinical experience and expertise in EQ-5D-5L and mRS administration, this flexible remote opportunity offers meaningful involvement in global stroke clinical trials.
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