Work from Home Clinical Data Associate Hiring at Cognitive Value Tech

Clinical Data Associate Hiring at Cognitive Value Tech

About the Job

Cognitive Value Tech is actively seeking Clinical Data Associates to join their team in a work-from-home setup. This is a great opportunity for professionals with 1 to 3 years of experience in clinical data management who are looking to contribute to the success of clinical research programs.

If you have expertise in edit checks, medical coding, CRF design, and clinical trial data management, this role is a perfect fit for you!

Key Responsibilities

1. Clinical Data Management

• Oversee data collection, validation, and cleaning to maintain accuracy and integrity.
• Work with Clinical Research Associates (CRAs) and biostatisticians to define data management protocols.
• Ensure compliance with FDA, ICH-GCP, and other regulatory standards.

2. Edit Check Design & Implementation

• Develop and execute edit checks to identify errors, inconsistencies, and missing data.
• Maintain and update edit check specifications to improve data quality.

3. Medical Coding

• Perform medical coding of adverse events, medical history, and medications using MedDRA and WHO Drug dictionaries.
• Resolve discrepancies in coding to ensure accuracy.

4. Case Report Form (CRF) Design

• Assist in designing electronic and paper CRFs for accurate data collection.
• Ensure CRF compliance with study protocols and regulatory requirements.

5. Quality Control & Data Validation

• Conduct regular quality control reviews to verify data consistency.
• Develop and manage data validation plans and query resolution processes.
• Coordinate with investigational sites for query resolution.

6. Reporting & Documentation

• Maintain detailed data management records.
• Generate reports and status updates for project teams.

Required Qualifications

• Education: Bachelor’s or Master’s degree in Life Sciences, Healthcare Informatics, Biotechnology, Pharmacy, or related fields.
• Experience: 1 to 3 years of hands-on experience in clinical data management.
• Proficiency in clinical data management software (EDC systems preferred).
• Knowledge of ICH-GCP, FDA regulations, and medical coding.
• Experience in MedDRA and WHO Drug coding.
• Strong skills in edit check creation, query resolution, and CRF design.
• Excellent analytical and problem-solving abilities.
• Effective communication and teamwork skills.
• Certifications in Clinical Data Management are a plus.

How to Apply?

Interested candidates can send their resumes to jobs@cognitivevaluetech.com.

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