6 Medicalcoding Jobs

Responsibilities: Conduct quality assurance audits of inpatient and outpatient coded records Perform detailed chart audits to identify coding errors and assess coder performance Analyze audit data and implement corrective action plans with coding teams Provide feedback, documentation support, and retraining as needed Work with cross-functional teams to resolve coding-related denials Ensure accurate code assignment to support revenue cycle management Interested to apply can share CV or call/WhatsApp to 9342735755

We are looking for a detail-oriented and motivated Associate Medical Coder to join our healthcare delivery team. The ideal candidate will be responsible for reviewing clinical documents and assigning appropriate ICD-10-CM and CPT/HCPCS codes for diagnoses and procedures, ensuring accuracy and compliance with industry standards. Responsibilities: Review patient medical records and accurately assign diagnosis and procedure codes using ICD-10-CM, CPT, and/or HCPCS Ensure compliance with government regulations and company coding guidelines Maintain confidentiality of patient health information Meet or exceed coding productivity and accuracy benchmarks Work closely with the coding quality team for audits and feedback Stay updated on changes in coding guidelines and payer-specific requirement. Interested to apply can share CV or call/WhatsApp to 9342735755

Roles and Responsibilities: Perform coding of Adverse Events , Medical History, Indications, and Concomitant Medications using MedDRA and WHO Drug Dictionary. Ensure accurate and consistent data entry within global safety databases. Review case narratives and source documents to assign appropriate codes. Maintain compliance with ICH, GVP, and company SOPs. Coordinate with case processors, medical reviewers, and QA teams to resolve coding discrepancies. Stay updated with MedDRA and WHO-DD version updates and apply changes. Participate in coding audits, quality control, and data consistency checks. Support safety signal detection and regulatory queries with coded data. Qualifications: Bachelors degree in Pharmacy, Life Sciences, Nursing, or related field 2-5+ years of experience in pharmacovigilance or medical coding Hands-on experience. Familiarity with PV software. Basic understanding of ICSR and pharmacovigilance workflow. Certification in pharmacovigilance or medical coding is preferred. Interested to apply can share CV or call/WhatsApp to 9342735755

We have an opportunity for certified HCC coders. - Minimum 6 months work experience for coder, Above 2 years of Work experience for QA/QC - Work Location: Ambattur IE, Chennai; no WFH will be provided. - Interview Mode: Virtual - Certification is mandatory (CPC, CRC, CCS, CIC, COC). (Shortlisted candidates should join us before 30th Jul 2025) Send an updated resume, a recent photo, Aadhar card, member ID with the mentioned details to WhatsApp, and your interview will be scheduled. For any other queries, kindly reach out & drop your resume on WhatsApp or call and discuss the interview schedule and process. Contact Name: Surendaran (HR) Contact Number: 9600183612

Hiring @Medmetrix Job Title: Operations Manager - IPDRG Specialty Location: RMZ Millenia, Perungudi, Chennai Work Mode: Work from Office Experience Required: 10+ Years Employment Type: Full Time, Permanent **Interested candidates can share their updated cv to hgayathri@med-metrix.com Job Description: We are hiring an experienced Operations Manager with a strong background in IPDRG (Inpatient Prospective Diagnosis Related Group) services. The ideal candidate will have over 10 years of experience in operations, with proven expertise in client handling , team leadership, and healthcare process optimization. Key Responsibilities: Lead and manage daily operations of the IPDRG division Ensure delivery of high-quality services in line with SLAs and compliance standards Build and maintain strong client relationships, acting as the primary point of contact Drive process improvements and operational efficiency Mentor and guide team members to achieve performance goals Desired Candidate Profile: Minimum 10 years of experience in operations, with at least 5 years in IPDRG Strong client-facing and stakeholder management skills Excellent communication and leadership abilities Bachelor's degree in Healthcare, Business, or related field (Masters preferred) Key Skills: Operations Management, IPDRG, Client Handling, Healthcare Services, Team Leadership, Process Improvement Salary: As per industry standards Regards. Harshini - HR hgayathri@med-metrix.com

Description We are seeking a highly motivated Medical Safety Physician with 3-8 years of experience to join our team. As a Medical Safety Physician, you will be responsible for ensuring patient safety and compliance with regulatory requirements. You will work closely with cross-functional teams to develop and implement safety strategies for our products. Responsibilities Develop and implement medical safety strategies for our products Manage safety-related issues and concerns from clinical trials through to post-marketing surveillance Ensure compliance with regulatory requirements and guidelines Provide medical expertise and guidance to cross-functional teams Conduct safety reviews of clinical trial protocols, study reports, and regulatory submissions Collaborate with internal and external stakeholders to assess and manage safety risks Participate in safety signal detection and assessment activities Contribute to the development and implementation of risk management plans Provide medical review of adverse event reports and ensure timely reporting to regulatory authorities Skills and Qualifications Medical degree (MBBS/MD) with 3-8 years of experience in medical safety or pharmacovigilance Knowledge of global regulatory requirements and guidelines related to drug safety Experience in safety surveillance and risk management activities Excellent analytical and problem-solving skills Ability to work independently and collaboratively in a cross-functional team environment Strong communication and interpersonal skills Attention to detail and ability to manage multiple tasks simultaneously Experience in conducting safety reviews of clinical trial protocols, study reports, and regulatory submissions