Strong interest in clinical research and drug development. Basic understanding of Good Clinical Practice (GCP) and clinical trial processes (training will be provided). Excellent attention to detail, communication, and organizational skills. Ability to manage time effectively and work in a team environment. Support the initiation, monitoring, and close-out of clinical trial sites under supervision. Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements. Job Types: Full-time, Permanent, Fresher Pay: ₹24,805.52 - ₹35,778.69 per month Benefits: Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person
Review and analyze patient medical records for proper coding. Assign correct ICD-10, CPT, and HCPCS codes based on medical documentation. Ensure accuracy and compliance with all coding policies and guidelines. Collaborate with physicians and other healthcare professionals for clarification when needed. Maintain confidentiality of patient records and information. Participate in ongoing coding training and professional development. Good understanding of human anatomy, physiology, and medical terminology. Strong attention to detail and analytical skills. Basic knowledge of ICD-10 and CPT coding systems. Job Types: Full-time, Permanent, Fresher Pay: ₹25,135.61 - ₹40,783.36 per month Benefits: Paid sick time Schedule: Day shift Work Location: In person
Assist in data entry, validation, and cleaning of clinical trial data. Work with Case Report Forms (CRFs) and electronic data capture (EDC) systems. Ensure data is accurate, consistent, and in accordance with study protocols. Support in the creation and testing of data validation checks. Perform quality control checks and resolve data queries under supervision. Collaborate with cross-functional teams including clinical operations and biostatistics. Maintain documentation and follow Standard Operating Procedures (SOPs). Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines. Job Types: Full-time, Permanent, Fresher Pay: ₹359,737.73 - ₹568,740.59 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Joining bonus Performance bonus Quarterly bonus Yearly bonus Work Location: In person
Ability to manage time effectively and work in a team environment. Support the initiation, monitoring, and close-out of clinical trial sites under supervision. Strong interest in clinical research and drug development. Basic understanding of Good Clinical Practice (GCP) and clinical trial processes (training will be provided). Excellent attention to detail, communication, and organizational skills. Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements. Job Types: Full-time, Permanent, Fresher Pay: ₹27,147.52 - ₹42,123.69 per month Benefits: Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person
Perform case intake and data entry into safety databases (e.g., Argus, ArisG). Assist in triaging and prioritizing cases based on seriousness and timelines. Perform quality checks to ensure accuracy and completeness of information. Collect and process adverse event (AE) reports from healthcare professionals, patients, and regulatory authorities Support Periodic Safety Update Reports (PSURs), Risk Management Plans (RMPs), Draft case narratives and perform medical coding (MedDRA). Job Type: Full-time Pay: ₹305,702.54 - ₹565,749.57 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Work Location: In person
Perform case intake and data entry into safety databases (e.g., Argus, ArisG). Assist in triaging and prioritizing cases based on seriousness and timelines. Perform quality checks to ensure accuracy and completeness of information. Collect and process adverse event (AE) reports from healthcare professionals, patients, and regulatory authorities Support Periodic Safety Update Reports (PSURs), Risk Management Plans (RMPs), Draft case narratives and perform medical coding (MedDRA). Job Type: Full-time Pay: ₹305,702.54 - ₹565,749.57 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Work Location: In person
Excellent attention to detail, communication, and organizational skills. Strong interest in clinical research and drug development Basic understanding of Good Clinical Practice (GCP) and clinical trial processes (training will be provided). Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements. Ability to manage time effectively and work in a team environment. Support the initiation, monitoring, and close-out of clinical trial sites under supervision. Job Types: Full-time, Permanent, Fresher Pay: ₹27,655.52 - ₹43,123.69 per month Benefits: Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person
Review and analyze patient medical records for proper coding. Assign correct ICD-10, CPT, and HCPCS codes based on medical documentation. Ensure accuracy and compliance with all coding policies and guidelines. Collaborate with physicians and other healthcare professionals for clarification when needed. Maintain confidentiality of patient records and information. Participate in ongoing coding training and professional development. Good understanding of human anatomy, physiology, and medical terminology. Strong attention to detail and analytical skills. Basic knowledge of ICD-10 and CPT coding systems. Job Types: Full-time, Permanent, Fresher Pay: ₹26,233.61 - ₹44,567.36 per month Benefits: Paid sick time Schedule: Day shift Work Location: In person
Collect, review, and process individual case safety reports (ICSRs) from clinical trials, post-marketing, and spontaneous sources. Perform medical coding using MedDRA and WHO-DD databases. Enter safety data into pharmacovigilance databases (e.g., Argus, ARISg, Veeva Vault Safety). Conduct case narrative writing and assessment of seriousness, expectedness, and causality. Prepare and submit reports to regulatory authorities (e.g., CIOMS, MedWatch, E2B submissions). Contribute to the preparation of aggregate safety reports (e.g., PSUR, DSUR, PADER). Job Types: Full-time, Permanent, Fresher Pay: ₹340,145.36 - ₹580,124.55 per year Benefits: Paid sick time Provident Fund Work from home Work Location: In person
Review and analyze patient medical records and documents for coding accuracy. Assign appropriate ICD-10, CPT, and HCPCS codes to diagnoses and procedures. Ensure proper coding to maximize reimbursement and reduce claim denials. Maintain coding quality and productivity standards. Collaborate with physicians and other healthcare staff to clarify diagnoses or obtain additional information. Stay up to date with changes in coding standards, compliance regulations, and payer requirements. Job Types: Full-time, Permanent, Fresher Pay: ₹22,937.66 - ₹37,469.29 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Work Location: In person
Excellent attention to detail, communication, and organizational skills. Strong interest in clinical research and drug development Basic understanding of Good Clinical Practice (GCP) and clinical trial processes (training will be provided). Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements. Ability to manage time effectively and work in a team environment. Support the initiation, monitoring, and close-out of clinical trial sites under supervision. Job Types: Full-time, Permanent, Fresher Pay: ₹27,655.52 - ₹43,123.69 per month Benefits: Paid sick time Work Location: In person
Learn and apply coding guidelines and principles as per current industry standards. Review patient medical records under supervision to identify diagnoses and procedures for coding. Assign appropriate codes using ICD-10, CPT, and HCPCS under trainer supervision. Collaborate with senior coders, auditors, and physicians for documentation improvement. Maintain productivity and accuracy standards as defined by the organization. Attend training sessions, webinars, and performance reviews regularly. Maintain confidentiality of patient records and comply with HIPAA regulations. Stay updated with changes in coding rules, payer requirements, and compliance guidelines Job Types: Full-time, Permanent, Fresher Pay: ₹19,882.93 - ₹35,490.87 per month Benefits: Health insurance Provident Fund Work Location: In person
Review and analyze medical records and physician documentation. Assign accurate ICD-10, CPT, and HCPCS codes for diagnoses, procedures, and services. Ensure compliance with official coding guidelines and legal regulations (e.g., HIPAA). Work with healthcare providers to clarify diagnoses and obtain additional information when needed. Assist in resolving coding-related billing issues or claim denials. Maintain up-to-date knowledge of coding standards, payer policies, and CMS regulations. Perform audits of clinical documentation and coded data to ensure accuracy and integrity. Collaborate with billing and compliance teams to optimize reimbursement. Job Types: Full-time, Permanent, Fresher Pay: ₹19,935.64 - ₹36,599.24 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
Assist in site selection, initiation, monitoring, and close-out visits. Ensure that clinical trials are conducted in accordance with protocols, SOPs, GCP, and regulatory requirements. Verify the accuracy and completeness of case report forms (CRFs) and source documents. Maintain essential documents in the Trial Master File (TMF). Assist in resolving data queries and discrepancies with the site staff. Support investigators and site staff in trial-related activities. Participate in project team meetings and training sessions. Prepare visit reports and follow-up letters. Maintain regular communication with study sites to ensure compliance and timely data entry. Job Types: Full-time, Permanent, Fresher Pay: ₹20,778.01 - ₹36,570.20 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
You have a strong interest in clinical research and drug development. You have a basic understanding of Good Clinical Practice (GCP) and clinical trial processes (training will be provided). Your attention to detail, communication, and organizational skills are excellent. You have the ability to manage time effectively and work in a team environment. You will support the initiation, monitoring, and close-out of clinical trial sites under supervision. You will also help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements. This is a Full-time, Permanent, and Fresher job opportunity. The benefits include paid sick time. The work schedule is during the day shift. There are performance bonuses and yearly bonuses offered. The work location is in person.,
Review patient records and clinical documents to extract relevant medical information. Assign standard diagnosis (ICD-10-CM) and procedure codes (CPT/HCPCS) according to coding guidelines. Work under supervision to ensure accurate and compliant coding practices. Communicate with healthcare providers for clarification on documentation when needed. Assist with claims processing and resolving coding-related billing issues or denials. Maintain compliance with HIPAA and data protection regulations. Stay current with coding updates, payer rules, and healthcare regulations. Participate in team meetings, training sessions, and continuous learning initiatives. Job Types: Full-time, Permanent, Fresher Pay: ₹19,916.28 - ₹35,405.50 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Work Location: In person
As a Data Entry Assistant in this role, you will be responsible for supporting the data management processes of clinical trial data in accordance with Good Clinical Data Management Practices (GCDMP). Your key tasks will include assisting in data entry, validation, and cleaning procedures to ensure accuracy and compliance. You will also play a crucial role in aiding the development and testing of Case Report Forms (CRFs) and electronic data capture (EDC) systems. Additionally, you will be tasked with managing discrepancies and data queries efficiently to address any data issues that may arise during the process. Maintaining detailed study-specific documentation, such as data management plans and data validation guidelines, will be part of your responsibilities. Collaboration with diverse teams including clinical research associates, biostatisticians, and programmers will be essential to ensure seamless data management operations. Furthermore, you will be involved in activities related to database lock and archiving, as well as participating in quality control procedures and audits to uphold data integrity standards. It will be imperative for you to familiarize yourself with and adhere to standard operating procedures (SOPs), ICH-GCP guidelines, and regulatory principles pertinent to clinical data management. This position offers full-time, permanent employment opportunities, making it an ideal fit for individuals looking to establish a career in data management within the clinical research domain. In addition to a dynamic work environment, the role comes with benefits such as health insurance and paid sick time. Please note that the work location for this position is on-site, requiring your presence in person to fulfill the responsibilities effectively.,
As a Safety Specialist, your primary responsibility will be to receive, triage, and process individual case safety reports (ICSRs) in a timely manner. You will accurately enter event data into PV databases and code medical terms using MedDRA / WHO-DD codes. It will be your duty to assess the seriousness, causality, and expectedness of cases, as well as conduct literature surveillance to identify potential safety signals. Additionally, you will play a key role in assisting with the preparation of case narratives, reports, and documentation. You will support the creation of aggregate safety reports such as PSURs and RMPs. Ensuring strict adherence to SOPs and regulatory standards will be crucial in this role. To qualify for this position, you should hold a Bachelors or Masters degree in Pharmacy, Life Sciences, Biotechnology, or a related field. You must possess excellent attention to detail and analytical capabilities. A basic understanding of medical terminology and drug safety processes is also required. This is a full-time, permanent position suitable for both experienced professionals and freshers. The work location will be in person, and benefits include health insurance, paid sick time, and paid time off.,