Clinical Reviewer

Job Summary:This position involves reviewing clinical documentation to ensure accuracy and completeness. Key responsibilities include reviewing medical records, collaborating with internal teams, and identifying documentation gaps.Review Clinical DocumentationEvaluate Compliance with Coding StandardsCollaborate with Internal TeamsSupport Documentation...

We are seeking an experienced and detail-oriented Medical Reviewer to join our team. The role involves reviewing, analyzing, and ensuring accuracy, consistency, and compliance of medical and scientific content in alignment with regulatory, clinical, and organizational standards.Key ResponsibilitiesReview medical, clinical, and regulatory documents for...

Medical Expert Job OverviewWe are seeking a Medical Expert to provide medical support to Clinical Program Leaders, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents, responses to Health Authority questions, and conducting ongoing review of clinical trial data.Key ResponsibilitiesContribute...

Job Summary:We are looking for a highly skilled and experienced Clinical Research Scientist with a strong background in Bioequivalence and Bioavailability (BE/BA) studies and clinical operations. The ideal candidate will have over 10 years of experience in the pharmaceutical industry, with a minimum of 7 years in BE/BA studies, and a deep understanding of...

Job OverviewA Medical Coder/Reviewer is responsible for reviewing patient medical records to ensure accurate coding and compliance with clinical guidelines.Key Responsibilities:Conduct thorough reviews of medical records to identify incorrectly coded services, diagnoses, modifiers, DRGs, APCs, and other coding irregularities.Perform regular coding audits to...

Clinical Documentation Specialist Role:We are seeking a skilled Clinical Documentation Specialist to join our team. In this critical role, you will review clinical documentation in electronic health records to ensure accuracy, completeness, and compliance with coding standards.Key Responsibilities Include:Conduct concurrent reviews of inpatient records using...

About UsWe are a global technology company that helps enterprises reimagine their businesses for the digital age.Deliver exceptional technology solutions by joining our team of talented professionals who contribute to our mission.About the RoleResponsibilities:Bachelor's degree in Life Sciences, Computer Science, or related field required.8+ years of...

We are seeking a talented individual to fill the role of Clinical Research Associate. This position involves performing user acceptance testing for clinical forms, database edit checks, and reports/listings.Applicants must possess a Bachelor's degree in Life Sciences or Computer Science.A minimum of 8 years of experience in clinical data testing and...

Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we're looking for experienced full-time, Hyderabad-based Data Review Associate to join us as we prepare to launch of our newest office inHyderabad, India.This is more than just a job. It's an opportunity to be part of something from the very beginning. You'll...

As a clinical data specialist, you will play a pivotal role in ensuring timely and efficient execution of clinical trials. Your primary responsibilities include contributing to operational/clinical trial deliverables, overseeing protocol development, and conducting study start-up activities.Key ResponsibilitiesContribute to all operational/clinical trial...