
51 - 200 employees
đź’Ľ Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
🔥 16 minutes ago
🇺🇸 United States – Remote
⏰ Full Time
đźź Senior
🏥 Medical Billing and Coding
🦅 H1B Visa Sponsor
đź‘» Ghost score 23%
Where this job comes from
Posted on Clinical Outcomes Solutions's careers page, not through a job board
First seen by Remote Rocketship 16 minutes ago

51 - 200 employees
đź’Ľ Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
• Perform complex medical coding for adverse events, medical history, procedures, and concomitant medications using MedDRA and WHODrug dictionaries • Review and validate coding performed by other coders to ensure consistency and accuracy • Identify ambiguous or unclear terms and query clinical sites for clarification • Maintain coding conventions and ensure alignment with study-specific and sponsor requirements • Conduct ongoing coding checks during data cleaning cycles and prior to database lock • Participate in the resolution of coding discrepancies, queries, and coding-related data issues • Review safety data for coding accuracy in collaboration with medical monitors and safety teams • Assist in preparing coding-related metrics, reports, and quality documentation • Participate in vendor oversight activities when coding tasks are outsourced • Stay current with updates to MedDRA and WHODrug dictionaries and communicate relevant changes to project teams • Work closely with clinical data management to ensure proper term collection and standardization • Partner with safety teams to support expedited reporting, signal detection, and regulatory submissions • Support biostatistics and medical writing with queries related to coded terms for analyses and study reports
• Proficient in Medidata RAVE and Coder • Strong working knowledge of MedDRA and WHODrug dictionaries, including version control and update management • Bachelor's degree in life sciences, nursing, pharmacy, public health, or equivalent healthcare background • 2 years of medical coding experience in clinical research • Experience supporting multiple therapeutic areas • Excellent understanding of ICH-GCP, FDA, EMA, and other global regulatory guidelines • Strong attention to detail, analytical problem-solving, and ability to manage multiple projects simultaneously • Effective communication skills and experience collaborating in matrixed research environments
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