Review and analyze medical records and documentation for accuracy and completeness. Assign appropriate ICD-10, CPT, and HCPCS codes based on provider documentation. Ensure coding aligns with federal regulations and payer-specific guidelines. Query healthcare providers when documentation is unclear or incomplete. Assist in claim denial management by correcting and resubmitting rejected claims. Maintain up-to-date knowledge of coding guidelines and insurance requirements. Collaborate with billing staff to ensure clean claim submissions. Participate in internal audits and quality improvement initiatives. Maintain patient confidentiality in compliance with HIPAA regulations. Job Types: Permanent, Fresher Pay: ₹20,058.08 - ₹44,674.97 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Review and analyze medical records and documentation for accuracy and completeness. Assign appropriate ICD-10, CPT, and HCPCS codes based on provider documentation. Ensure coding aligns with federal regulations and payer-specific guidelines. Query healthcare providers when documentation is unclear or incomplete. Assist in claim denial management by correcting and resubmitting rejected claims. Maintain up-to-date knowledge of coding guidelines and insurance requirements. Collaborate with billing staff to ensure clean claim submissions. Participate in internal audits and quality improvement initiatives. Maintain patient confidentiality in compliance with HIPAA regulations. Job Types: Permanent, Fresher Pay: ₹20,058.08 - ₹44,674.97 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Monitor clinical trial sites to ensure compliance with study protocols, GCP, and regulatory requirements. Perform site initiation, routine monitoring, and close-out visits. Assist in the preparation of regulatory submissions and documentation. Provide training and support to site staff as needed. Review and verify case report forms (CRFs) against source documents. Identify and resolve data discrepancies. Ensure proper documentation and timely reporting of adverse events. Job Types: Permanent, Fresher Pay: ₹25,001.03 - ₹40,100.97 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person
Assign appropriate ICD-10, CPT, and HCPCS codes based on provider documentation.. Query healthcare providers when documentation is unclear or incomplete. Assist in claim denial management by correcting and resubmitting rejected claims. Maintain up-to-date knowledge of coding guidelines and insurance requirements. Collaborate with billing staff to ensure clean claim submissions. Participate in internal audits and quality improvement initiatives. Maintain patient confidentiality in compliance with HIPAA regulations. Review and analyze medical records and documentation for accuracy and completeness. Job Types: Permanent, Fresher Pay: ₹23,238.08 - ₹45,145.97 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Assist in setting up, monitoring, and closing clinical trial sites under supervision. Ensure trials are conducted in accordance with ICH-GCP guidelines, regulatory requirements, and company SOPs. Perform on-site and remote monitoring visits to ensure data integrity and subject safety. Review case report forms (CRFs) for completeness, accuracy, and consistency. Assist with study documentation including investigator site files (ISFs), trial master files (TMFs), and essential documents. Collaborate with investigators, site staff, and internal teams to support smooth trial execution. Track and manage study supplies and ensure compliance with study protocols. Participate in investigator meetings, site initiation visits, and training sessions. Job Types: Full-time, Permanent, Fresher Pay: ₹22,821.77 - ₹35,967.25 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person
Collect, review, and process adverse event reports from clinical trials, post-marketing sources, and literature. Ensure timely and accurate entry of safety data into safety databases (e.g., Argus, ARISg). Prepare and submit Individual Case Safety Reports (ICSRs) to regulatory authorities within stipulated timelines. Conduct follow-ups with healthcare providers or patients for missing information. Assist in the preparation of Periodic Safety Update Reports (PSURs), Development Safety Update Reports (DSURs), and Risk Management Plans (RMPs). Monitor global pharmacovigilance regulatory requirements and ensure compliance. Collaborate with cross-functional teams such as Regulatory Affairs, Medical Affairs, and Clinical Operations. Participate in signal detection and safety data review activities. Job Types: Permanent, Fresher Pay: ₹356,822.62 - ₹601,606.13 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Assign appropriate ICD-10, CPT, and HCPCS codes based on provider documentation.. Query healthcare providers when documentation is unclear or incomplete. Assist in claim denial management by correcting and resubmitting rejected claims. Maintain up-to-date knowledge of coding guidelines and insurance requirements. Participate in internal audits and quality improvement initiatives. Review and analyze medical records and documentation for accuracy and completeness. Maintain patient confidentiality in compliance with HIPAA regulations. Job Types: Full-time, Permanent, Fresher Pay: ₹22,142.96 - ₹40,731.79 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Monday to Friday Supplemental Pay: Overtime pay Performance bonus Yearly bonus Work Location: In person
Assist in entering safety data into pharmacovigilance databases (e.g., Argus, ARISg). Perform initial coding of medical terms using MedDRA and drugs using WHO-DD. Support the preparation of case narratives and regulatory reports. Ensure all activities comply with applicable regulatory guidelines (GVP, ICH, FDA). Participate in internal training programs to build knowledge in drug safety and pharmacovigilance practices. Collaborate with senior team members on various projects and documentation tasks. Job Types: Full-time, Permanent, Fresher Pay: ₹358,180.92 - ₹670,989.55 per year Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
As a Data Management Specialist, you will be responsible for designing and reviewing Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. You will develop and maintain Data Management Plans (DMPs), data validation specifications, edit checks, and coding guidelines. Your role will involve overseeing data entry, data cleaning, discrepancy management, and query resolution processes to ensure data integrity. It will be your responsibility to ensure compliance with industry standards such as CDISC (CDASH, SDTM) and regulatory guidelines from FDA and ICH-GCP. You will be involved in conducting User Acceptance Testing (UAT) of EDC systems and monitoring data quality throughout the project lifecycle. Additionally, you will work towards achieving timely database lock in accordance with project schedules. This is a full-time and permanent position suitable for fresher candidates. The benefits of this role include health insurance, paid sick time, and Provident Fund. The work location for this role is in person, where you will collaborate with a team to achieve data management goals efficiently.,
As a Clinical Trials Assistant, you will play a crucial role in supporting various aspects of clinical trials. Your responsibilities will include assisting in site selection, initiation, monitoring, and close-out visits for clinical trials to ensure their successful implementation. It will be your responsibility to ensure that all clinical trials are conducted in compliance with the protocol, ICH-GCP guidelines, and regulatory requirements. You will be tasked with maintaining accurate and proper documentation of all trial activities and reporting findings effectively. Your role will also involve supporting data verification by meticulously comparing source data with Case Report Forms (CRFs). Effective communication with investigators and site staff will be essential to address and resolve any issues that may arise during the trials. In addition, you will be expected to assist in tracking project timelines and deliverables to ensure the smooth progression of the trials. It will also be necessary for you to attend training sessions regularly to stay updated with the latest regulatory guidelines and industry standards. This is a full-time, permanent position suitable for freshers who are looking to kickstart their career in the field of clinical trials. The benefits of this position include health insurance, paid sick time, and Provident Fund. The work location for this role is in person, providing you with a hands-on experience in the clinical trials environment.,
Assist in setting up, monitoring, and closing clinical trial sites under supervision. Ensure trials are conducted in compliance with protocols, ICH-GCP guidelines, and regulatory requirements. Perform site visits (remote or on-site) and assist with source data verification. Maintain study documentation and track essential documents. Support the collection, review, and submission of trial-related documentation (e.g., informed consent forms, CRFs). Assist with training site staff on study protocols and procedures. Collaborate with cross-functional teams, including project managers, data managers, and regulatory staff. Report any deviations, issues, or safety concerns to the study lead. Participate in internal training programs to gain knowledge of clinical trial processes. Job Types: Full-time, Fresher Pay: ₹22,800.49 - ₹38,652.15 per month Benefits: Health insurance Paid sick time Paid time off Work Location: In person
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