Medical Coder – Contract

Job not on LinkedIn

🔥 0 minutes ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $80k - $105k / year

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🏥 Medical Billing and Coding

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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eClinical Solutions

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2012

💼 Consulting

🏥 Healthcare

🧬 Biotechnology

💰 Private Equity Round on 2020-01

Consulting • Healthcare • Biotechnology

eClinical Solutions is a clinical data management company that provides integrated data review and management solutions for the biotech and pharmaceutical industries. Their platform, elluminate, empowers organizations to modernize and automate their clinical data workflows, ensuring efficient data acquisition, management, and analysis. By leveraging advanced analytics and technology-driven approaches, eClinical Solutions helps streamline trial operations and improve productivity, enabling better decision-making in clinical research.

📋 Description

• Serve as the lead coding resource for assigned clinical trials • Design and maintain Medical Coding Guidelines and Serious Adverse Event reconciliation plans with sponsors • Perform medical coding using WHODrug and MedDRA dictionaries • Review coding accuracy and consistency, including approval of coded terms and synonym lists • Reconcile serious adverse events across clinical trial databases, safety systems, and other sources • Generate coding and SAE queries as necessary • Collaborate with safety, clinical, and data management teams to resolve discrepancies • Document coding decisions and justifications for auditability • Assist with coding tool maintenance, including UAT script creation and execution • Participate in MedDRA and WHODrug dictionary versioning workflows • Test coding tools and deploy coding/SAE listings in elluminate • Ensure compliance with company and industry quality standards, regulations, guidelines, and procedures • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree in relevant health science or professional qualification in a relevant scientific/technical discipline preferred • 5+ years’ experience in the Pharmaceutical/Biotechnology industry with medical coding experience using WHODrug and MedDRA preferred • Knowledge of industry standards, ICH guidelines, and regulatory requirements for medical coding • Strong knowledge of ICH/GCP guidelines, 21 CFR Part 11, and clinical trial methodology • Excellent verbal and written communication skills • Detail oriented, with multitasking, prioritization, planning, and organization skills • Ability to work independently and in a team setting

🏖️ Benefits

• Remote work • Work-life balance • Opportunities to learn, grow, and continuously improve • Inclusive culture valuing diversity • Equal opportunity employment