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
Assist in reviewing patient records and clinical documentation to identify appropriate codes. Learn and apply basic coding guidelines (ICD-10, CPT, HCPCS) under supervision. Collaborate with senior coders, physicians, and billing teams to ensure accurate coding and documentation. Participate in ongoing training, workshops, and seminars related to coding and compliance. Maintain confidentiality of patient records in compliance with HIPAA regulations. Perform quality checks on coded data to identify potential errors or inconsistencies. Support the billing team in resolving coding-related denials or rejections. Stay updated on current coding standards, insurance regulations, and healthcare policies. Job Types: Full-time, Permanent, Fresher Pay: ₹23,916.28 - ₹40,405.50 per month Work Location: In person
Prepare, review, and submit medical claims to insurance companies (electronically and paper). Verify patient insurance coverage and benefits. Follow up on unpaid or denied claims; initiate appeals or re-submissions as necessary. Post payments and reconcile accounts accurately. Work with insurance companies, patients, and providers to resolve billing issues. Ensure compliance with HIPAA regulations and coding guidelines (ICD-10, CPT, HCPCS). Review patient bills for accuracy and completeness before sending out statements. Maintain detailed and organized billing records and documentation. Communicate with medical staff to clarify diagnoses or obtain additional information. Job Types: Full-time, Permanent, Fresher Pay: ₹19,664.74 - ₹35,552.64 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
Assist in the coordination and conduct of clinical trials under supervision Support patient recruitment, screening, and enrollment according to protocol criteria Schedule and manage patient visits, sample collection, and follow-ups Collect and accurately enter data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems Maintain essential documents in the Investigator Site File (ISF) Ensure adherence to study protocols, ICH-GCP, and regulatory requirements Assist in the preparation for audits or monitoring visits Communicate with sponsors, CROs, and ethics committees as needed Ensure timely reporting of adverse events and protocol deviations Support inventory management of study drugs, lab kits, and trial materials Job Types: Full-time, Permanent, Fresher Pay: ₹19,715.80 - ₹34,468.52 per month Benefits: Health insurance Paid sick time Work Location: In person
Assist in monitoring clinical trials at investigational sites under supervision Ensure compliance with ICH-GCP guidelines, regulatory requirements, and company SOPs Support site initiation, routine monitoring, and close-out visits Help in verifying source data and case report forms (CRFs) Maintain study documentation and track trial progress Assist in identifying and resolving site issues and deviations Coordinate with investigators, site staff, and internal study team Participate in training programs and development activities Prepare visit reports and documentation under supervision Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field Job Types: Full-time, Permanent, Fresher Pay: ₹23,858.48 - ₹38,990.58 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
Assist in the coordination and conduct of clinical trials under supervision Support patient recruitment, screening, and enrollment according to protocol criteria Schedule and manage patient visits, sample collection, and follow-ups Collect and accurately enter data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems Maintain essential documents in the Investigator Site File (ISF) Ensure adherence to study protocols, ICH-GCP, and regulatory requirements Assist in the preparation for audits or monitoring visits Communicate with sponsors, CROs, and ethics committees as needed Ensure timely reporting of adverse events and protocol deviations Support inventory management of study drugs, lab kits, and trial materials Job Types: Full-time, Permanent, Fresher Pay: ₹19,715.80 - ₹34,468.52 per month Benefits: Health insurance Paid sick time Work Location: In person
Assist in the preparation and coordination of clinical trial protocols and associated documents. Support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close-out. Ensure that study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements. Conduct site visits to assess the progress of clinical trials, monitor data accuracy, and ensure patient safety. Communicate with investigators and site staff to address issues or concerns related to the clinical trials. Assist in the review and management of clinical trial documentation, including case report forms (CRFs), informed consent forms, and regulatory submissions. Maintain study files and data to ensure compliance with applicable regulatory agencies. Support the clinical team in preparing reports, including monitoring reports and other regulatory documents. Attend and participate in internal meetings, as well as relevant training sessions, to develop knowledge and skills in clinical research. Job Types: Full-time, Fresher Pay: ₹22,869.01 - ₹38,019.71 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
Collect, review, and process adverse event reports from healthcare professionals, patients, and clinical studies. Enter and maintain accurate case data in safety databases. Perform case assessment and narrative writing under supervision. Assist in the preparation of Individual Case Safety Reports (ICSRs) and follow-up activities. Support signal detection and risk assessment processes. Ensure compliance with global pharmacovigilance regulations and company SOPs. Coordinate with cross-functional teams such as regulatory affairs, medical affairs, and clinical research. Participate in audits and inspections as needed. Job Types: Full-time, Permanent, Fresher Pay: ₹261,554.81 - ₹581,394.30 per year Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person
As an Assistant in this role, you will assist in the coordination and conduct of clinical trials under supervision. Your key responsibilities will include: - Supporting patient recruitment, screening, and enrollment according to protocol criteria - Scheduling and managing patient visits, sample collection, and follow-ups - Collecting and accurately entering data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems - Maintaining essential documents in the Investigator Site File (ISF) - Ensuring adherence to study protocols, ICH-GCP, and regulatory requirements - Assisting in the preparation for audits or monitoring visits - Communicating with sponsors, CROs, and ethics committees as needed - Ensuring timely reporting of adverse events and protocol deviations - Supporting inventory management of study drugs, lab kits, and trial materials Qualifications required for this position include: - Background in healthcare, life sciences, or related field - Knowledge of clinical trial processes and regulations - Strong attention to detail and organizational skills - Good communication and interpersonal abilities - Ability to work effectively in a team environment (Note: No additional details of the company were mentioned in the provided job description),
Assist in the initiation, monitoring, and closeout of clinical trial sites. Help prepare and review study materials, including patient recruitment documents, informed consent forms, and study protocol. Coordinate with site personnel to ensure that they have the necessary resources and training to conduct the study. Support efforts to recruit and retain patients for clinical trials by ensuring the study is conducted ethically and per protocol. Monitor patient enrollment and follow-up visits, ensuring compliance with the study timeline. Assist in the collection of clinical trial data and ensure proper documentation in the Case Report Form (CRF). Ensure the accuracy, completeness, and timeliness of data entry, and report discrepancies or inconsistencies. Participate in site monitoring visits (with a senior CRA or independently as experience grows). Ensure that sites are adhering to the study protocol, regulatory requirements, and GCP guidelines. Help resolve any issues found during monitoring visits, including site non-compliance, missing data, or patient safety concerns. Job Types: Full-time, Permanent, Fresher Pay: ₹22,885.55 - ₹43,331.46 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
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