Key Responsibilities: Design and analyze clinical and observational studies related to cost-effectiveness and health outcomes Support development and validation of economic models (e.g., Markov, decision trees) Conduct sensitivity analyses and interpret statistical outputs for economic evaluations Collaborate with health economists, epidemiologists, and clinical researchers Prepare statistical reports, manuscripts, and submissions for health authorities and payers Job Type: Full-time Pay: ₹299,054.61 - ₹1,624,327.89 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Pharmacovigilance Responsibilities- Monitoring and documenting adverse events and product complaints. Collaborating with cross-functional teams to ensure compliance with safety regulations. Preparing and submitting safety reports to health authorities. Contributing to the development of pharmacovigilance processes and procedures. Staying up-to-date with evolving pharmacovigilance guidelines and best practices Requirements And Skills- Bachelor’s degree in pharmacy, life sciences, or a related field. Strong understanding of pharmacovigilance regulations and guidelines. Excellent attention to detail and analytical skills. Effective communication and teamwork abilities. Proficiency in pharmacovigilance software and databases. Job Types: Full-time, Permanent, Fresher Pay: ₹19,191.63 - ₹48,236.01 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person
Key Responsibilities Client interaction:- Understand customer needs, answer basic queries, and explain offerings clearly. Follow-ups & appointment setting:- Follow up with warm leads and schedule meetings or demos for the senior sales team. Data entry & reporting:- Maintain accurate call records in CRM or Excel and report daily/weekly progress. About Company: Here at Refined Reports Data, we take pride in our champion customer support team. Ensuring customer satisfaction is of utmost importance to us, so feel free to ask us anything, anytime. You can also schedule a free-of-cost consultation regarding your needs with one of our professionals, and also get a quote ready at the earliest. Show more Show less
Responsibilities: Monitor clinical trials to ensure adherence to protocols and regulations. Conduct site visits to verify data accuracy and compliance. Assist in patient recruitment and ensure informed consent procedures. Maintain trial documentation and report findings to stakeholders. Ensure proper handling and storage of investigational drugs. Collaborate with investigators, sponsors, and regulatory authorities. Key Skills: Attention to Detail: Ensuring accuracy in trial data and documentation. Regulatory Knowledge: Understanding of GCP, FDA, and ICH guidelines. Communication Skills: Effective interaction with research teams and sponsors. Problem-Solving: Addressing challenges in trial execution. Project Management: Coordinating multiple aspects of clinical studies. Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Skills & Qualifications: Bachelor of Science (or higher) in Biological Sciences, Pharmacology, Toxicology, Chemistry or related Health Sciences Graduate Certificate in Pharmaceutical Regulatory Affairs Must have a minimum of four years of experience filing regulatory submissions with Health Canada Must have strong technical knowledge of CMC requirements and is able to critically analyze scientific data Strong interpersonal skills and ability to foster strong working relationships with key stakeholders (internally and externally) and representatives from Health Canada Strong working knowledge of Canadian Food and Drugs Act and Food and Drug Regulations, GMPs, ICH Guidelines and Health Canada Policies and Guidelines Knowledge of the Medical Devices Regulations is an asset Ability to prioritize workload to ensure all deadlines are met Experience with publishing eCTD submissions is an asset Ability to work independently with minimal supervision Excellent organization, written and oral communication skills Ability to effectively manage multiple projects in a fast-pace, results oriented environment Strong commitment to quality, accuracy and detail Ability to work well under pressure in a team based environment Strong problem solving/analytical ability and issue resolution skills Drug Regulatory Affairs Specialist Responsibilities & Duties Develop and implement regulatory strategies to bring drugs to market in compliance with relevant laws and regulations. Conduct regulatory research and provide guidance on regulatory issues and requirements. Prepare and submit applications and regulatory submissions, such as INDs, NDAs, and BLAs. Communicate with regulatory agencies and respond to inquiries. Manage projects and timelines to ensure timely submission of regulatory documents. Work with cross-functional teams to ensure regulatory compliance throughout the product development process. Stay informed of regulatory changes and trends in the industry. Job Types: Permanent, Fresher Pay: ₹25,217.75 - ₹45,679.31 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Monday to Friday Supplemental Pay: Performance bonus Yearly bonus Work Location: In person
Responsibilities: Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post-marketing surveillance. Ensure compliance with regulatory guidelines for drug safety reporting. Prepare and submit safety reports to regulatory authorities. Collaborate with healthcare professionals to assess and manage drug-related risks. Maintain and update safety databases with accurate information. Key Skills: Attention to Detail: Precision in analyzing and documenting safety data. Regulatory Knowledge: Familiarity with FDA, EMA, and ICH-GCP guidelines. Communication Skills: Ability to convey safety findings effectively. Analytical Thinking: Assessing risks and identifying safety signals. Team Collaboration: Working with cross-functional teams in pharmacovigilance. Job Type: Full-time Pay: ₹350,000.00 - ₹975,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Key Responsibilities: Accurately document patient history, physical exams, diagnoses, treatment plans, and other relevant information as dictated by the healthcare provider during patient visits. Enter data into Electronic Health Records (EHR) promptly and accurately. Ensure all documentation complies with medical, legal, and regulatory standards. Maintain patient confidentiality and follow HIPAA guidelines. Assist providers with administrative tasks related to medical documentation as needed. Review and update patient charts for accuracy and completeness. Collaborate with healthcare team members to facilitate efficient patient flow. Qualifications: degree in a health-related field preferred. Prior experience as a medical scribe or in healthcare documentation is a plus. Strong knowledge of medical terminology, anatomy, and healthcare procedures. Proficient computer skills, especially with EHR systems. Excellent attention to detail and strong organizational skills. Ability to multitask and work efficiently in a fast-paced clinical environment. Strong communication skills and ability to work well with healthcare professionals. Working Conditions: Typically works in a clinical or hospital setting alongside healthcare providers. May require standing or sitting for extended periods. Work hours may vary depending on clinic or hospital schedules. Job Type: Permanent Pay: ₹21,372.85 - ₹58,941.73 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Morning shift Work Location: In person
Key Responsibilities: Accurately document patient history, physical exams, diagnoses, treatment plans, and other relevant information as dictated by the healthcare provider during patient visits. Enter data into Electronic Health Records (EHR) promptly and accurately. Ensure all documentation complies with medical, legal, and regulatory standards. Maintain patient confidentiality and follow HIPAA guidelines. Assist providers with administrative tasks related to medical documentation as needed. Review and update patient charts for accuracy and completeness. Collaborate with healthcare team members to facilitate efficient patient flow. Qualifications: degree in a health-related field preferred. Prior experience as a medical scribe or in healthcare documentation is a plus. Strong knowledge of medical terminology, anatomy, and healthcare procedures. Proficient computer skills, especially with EHR systems. Excellent attention to detail and strong organizational skills. Ability to multitask and work efficiently in a fast-paced clinical environment. Strong communication skills and ability to work well with healthcare professionals. Working Conditions: Typically works in a clinical or hospital setting alongside healthcare providers. May require standing or sitting for extended periods. Work hours may vary depending on clinic or hospital schedules. Job Type: Permanent Pay: ₹21,372.85 - ₹58,941.73 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Morning shift Work Location: In person
Key Responsibilities: Review Patient Records: Examine clinical documents, including physician notes, lab reports, and test results, to determine the correct medical codes. Code Diagnoses and Procedures: Apply ICD-10 codes for diagnoses and CPT/HCPCS codes for procedures to ensure correct coding of services rendered. Ensure Accuracy: Ensure that coding is accurate, up-to-date, and compliant with insurance company and regulatory standards. Documentation and Compliance: Maintain accurate records for auditing purposes and comply with legal and ethical standards, including confidentiality regulations (HIPAA in the U.S.). Billing Support: Work with healthcare providers and medical billers to ensure that claims are processed efficiently and that reimbursements are received. Claim Management: Identify and resolve issues or discrepancies in coding that may lead to rejected claims. Stay Current with Coding Updates: Keep up-to-date with new codes, billing guidelines, and changes in medical regulations to maintain proficiency. Communicate with Healthcare Providers: Collaborate with physicians, nurses, and other healthcare professionals to clarify patient diagnoses and procedures. Skills & Qualifications: Certification: Certification from recognized bodies such as the American Health Information Management Association (AHIMA) or the American Academy of Professional Coders (AAPC) is often required. Knowledge of Coding Systems: Familiarity with ICD-10, CPT, and HCPCS coding systems, as well as an understanding of medical terminology and anatomy. Attention to Detail: High level of accuracy when assigning codes, as errors can lead to insurance disputes or payment delays. Analytical Skills: Ability to review and analyze medical records and translate them into appropriate codes. Computer Skills: Proficiency in coding software, medical record systems, and billing software. Communication Skills: Good written and verbal communication skills to interact with other healthcare professionals and ensure accurate coding. Preferred Qualifications: Knowledge of insurance policies, claim filing, and reimbursement processes. Familiarity with healthcare regulations and standards, including HIPAA Job Types: Full-time, Permanent Pay: ₹30,644.55 - ₹41,929.61 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
Key Responsibilities : Study Planning & Preparation : Assist in the development of study protocols, informed consent documents, and other study-related documents. Collaborate with Principal Investigators (PIs) and other clinical staff to ensure the research study is ready for initiation. Ensure that all study materials (e.g., consent forms, case report forms) are organized and accessible. Participant Recruitment & Retention : Recruit, screen, and enroll study participants based on inclusion/exclusion criteria. Maintain clear communication with participants throughout the study. Provide participants with detailed study information and obtain informed consent. Address any participant concerns and ensure compliance with study procedures. Data Collection & Management : Collect, record, and maintain accurate clinical data as per study protocols. Monitor the progress of the study, ensuring accurate data collection and documentation. Handle study samples (e.g., blood, urine) and ensure proper storage and transport as required. Maintain study-related records in accordance with Good Clinical Practice (GCP) and regulatory standards. Regulatory Compliance : Ensure that the study complies with all regulatory requirements, including those set forth by the FDA, IRBs, and other governing bodies. Prepare and submit regulatory documents to IRBs (Institutional Review Boards) and other regulatory agencies. Monitor participant safety and report any adverse events to the PI and regulatory bodies. Keep up-to-date with changes in clinical research regulations and guidelines. Study Monitoring & Reporting : Perform regular monitoring of the clinical trial to ensure compliance with the protocol. Report study progress and findings to the Principal Investigator and other stakeholders. Ensure that all study milestones and deadlines are met. Organize and participate in study meetings and site visits. Budget & Resource Management : Assist with the management of study budgets, including coordinating the ordering of study supplies and ensuring costs stay within the allocated budget. Ensure proper equipment and resources are available for study procedures. Safety Monitoring : Ensure that participant safety is monitored throughout the trial. Report and document any adverse events or unanticipated problems to the appropriate authorities. Training & Support : Provide training and guidance to junior staff or new coordinators. Support clinical trial staff with any operational challenges or questions. Qualifications : Education : Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Healthcare) Skills : Strong organizational and time-management skills. Excellent written and verbal communication. Ability to work independently as well as part of a team. Knowledge of clinical trial management software (e.g., EDC, CTMS). Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Working Conditions : Location : Clinical research sites, hospitals, academic medical centers, or offices. Hours : Typically full-time; may involve evening or weekend work depending on study needs. Travel : May require occasional travel to other study sites or regulatory meetings. Key Attributes : Detail-oriented and thorough. Able to work under pressure and meet deadlines. Strong ethical standards and a commitment to participant welfare. Job Types: Full-time, Permanent Pay: ₹30,086.00 - ₹40,006.71 per month Benefits: Health insurance Provident Fund Work Location: In person
Key Responsibilities: Review Patient Records: Examine clinical documents, including physician notes, lab reports, and test results, to determine the correct medical codes. Code Diagnoses and Procedures: Apply ICD-10 codes for diagnoses and CPT/HCPCS codes for procedures to ensure correct coding of services rendered. Ensure Accuracy: Ensure that coding is accurate, up-to-date, and compliant with insurance company and regulatory standards. Documentation and Compliance: Maintain accurate records for auditing purposes and comply with legal and ethical standards, including confidentiality regulations (HIPAA in the U.S.). Billing Support: Work with healthcare providers and medical billers to ensure that claims are processed efficiently and that reimbursements are received. Claim Management: Identify and resolve issues or discrepancies in coding that may lead to rejected claims. Stay Current with Coding Updates: Keep up-to-date with new codes, billing guidelines, and changes in medical regulations to maintain proficiency. Communicate with Healthcare Providers: Collaborate with physicians, nurses, and other healthcare professionals to clarify patient diagnoses and procedures. Skills & Qualifications: Certification: Certification from recognized bodies such as the American Health Information Management Association (AHIMA) or the American Academy of Professional Coders (AAPC) is often required. Knowledge of Coding Systems: Familiarity with ICD-10, CPT, and HCPCS coding systems, as well as an understanding of medical terminology and anatomy. Attention to Detail: High level of accuracy when assigning codes, as errors can lead to insurance disputes or payment delays. Analytical Skills: Ability to review and analyze medical records and translate them into appropriate codes. Computer Skills: Proficiency in coding software, medical record systems, and billing software. Communication Skills: Good written and verbal communication skills to interact with other healthcare professionals and ensure accurate coding. Preferred Qualifications: Knowledge of insurance policies, claim filing, and reimbursement processes. Familiarity with healthcare regulations and standards, including HIPAA Job Types: Full-time, Permanent Pay: ₹30,644.55 - ₹41,929.61 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
The responsibilities for this role include collecting and analyzing data on adverse drug reactions (ADRs) from clinical trials and post-market surveillance, preparing and submitting safety reports to regulatory authorities, ensuring compliance with pharmacovigilance regulations and guidelines, collaborating with healthcare professionals to assess and manage drug-related risks, and maintaining and updating safety databases with accurate information. Key skills required for this position are attention to detail for precision in analyzing and documenting safety data, regulatory knowledge including familiarity with FDA, EMA, and ICH-GCP guidelines, communication skills to effectively convey safety findings, analytical thinking for assessing risks and identifying safety signals, and team collaboration for working with cross-functional teams in pharmacovigilance. This is a full-time job opportunity with benefits including health insurance and provident fund. The work location for this position is in person.,
Drug Regulatory Affairs Specialist Responsibilities & Duties Develop and implement regulatory strategies to bring drugs to market in compliance with relevant laws and regulations. Conduct regulatory research and provide guidance on regulatory issues and requirements. Prepare and submit applications and regulatory submissions, such as INDs, NDAs, and BLAs. Communicate with regulatory agencies and respond to inquiries. Manage projects and timelines to ensure timely submission of regulatory documents. Work with cross-functional teams to ensure regulatory compliance throughout the product development process. Stay informed of regulatory changes and trends in the industry. Drug Regulatory Affairs Specialist Qualifications & Skills degree in pharmacy, life sciences, or a related field. Professional certification in regulatory affairs (e.g., RAC). Familiarity with electronic submission standards (eCTD). Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP). Strong project management skills. Proven ability to work in a fast-paced, deadline-driven environment. Bachelor's or Master's degree in a relevant field, such as pharmaceuticals, biology, or chemistry. Strong knowledge of FDA regulations and processes. Excellent project management skills. Excellent written and verbal communication skills. Ability to work well in a team environment. Job Types: Full-time, Permanent, Fresher Pay: ₹30,908.99 - ₹45,098.74 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
As a member of our healthcare team, you will be responsible for accurately documenting patient history, physical exams, diagnoses, treatment plans, and other relevant information as dictated by the healthcare provider during patient visits. Your key duties will involve entering this data promptly and accurately into Electronic Health Records (EHR), ensuring all documentation complies with medical, legal, and regulatory standards, and maintaining patient confidentiality according to HIPAA guidelines. Additionally, you will assist providers with administrative tasks related to medical documentation, review and update patient charts, and collaborate with other healthcare team members to facilitate efficient patient flow. The ideal candidate for this role will possess a degree in a health-related field, although prior experience as a medical scribe or in healthcare documentation will be considered a plus. It is essential to have a strong knowledge of medical terminology, anatomy, and healthcare procedures, as well as proficient computer skills, especially with EHR systems. Attention to detail, organizational skills, the ability to multitask, and work efficiently in a fast-paced clinical environment are also key qualities we are looking for. Strong communication skills and the ability to work well with healthcare professionals are highly valued in this position. You can expect to work in a clinical or hospital setting alongside healthcare providers, with the possibility of standing or sitting for extended periods. Your work hours may vary depending on clinic or hospital schedules, and this position is of a permanent nature. In addition to a challenging and rewarding work environment, we offer benefits such as health insurance, paid sick time, and Provident Fund. The schedule for this position is a day shift, morning shift, and the work location is in person. If you meet the qualifications and are excited about the opportunity to contribute to our healthcare team, we encourage you to apply for this position.,
Responsibilities: Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post-marketing surveillance. Ensure compliance with regulatory guidelines for drug safety reporting. Prepare and submit safety reports to regulatory authorities. Collaborate with healthcare professionals to assess and manage drug-related risks. Maintain and update safety databases with accurate information. Key Skills: Attention to Detail: Precision in analyzing and documenting safety data. Regulatory Knowledge: Familiarity with FDA, EMA, and ICH-GCP guidelines. Communication Skills: Ability to convey safety findings effectively. Analytical Thinking: Assessing risks and identifying safety signals. Team Collaboration: Working with cross-functional teams in pharmacovigilance. Job Type: Full-time Pay: ₹350,000.00 - ₹975,000.00 per year Benefits: Health insurance Provident Fund Work Location: In person
Responsibilities: Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post-marketing surveillance. Ensure compliance with regulatory guidelines for drug safety reporting. Prepare and submit safety reports to regulatory authorities. Collaborate with healthcare professionals to assess and manage drug-related risks. Maintain and update safety databases with accurate information. Key Skills: Attention to Detail: Precision in analyzing and documenting safety data. Regulatory Knowledge: Familiarity with FDA, EMA, and ICH-GCP guidelines. Communication Skills: Ability to convey safety findings effectively. Analytical Thinking: Assessing risks and identifying safety signals. Team Collaboration: Working with cross-functional teams in pharmacovigilance. Job Type: Full-time Pay: ₹350,000.00 - ₹975,000.00 per year Benefits: Health insurance Provident Fund Work Location: In person
Key Responsibilities Assist in recruitment and onboarding processes Maintain employee records and HR documentation Coordinate training programs and workshops Track training attendance and effectiveness Support HR initiatives and employee engagement activities Liaise with trainers, vendors, and departments for training needs About Company: Here at Refined Reports Data, we take pride in our champion customer support team. Ensuring customer satisfaction is of utmost importance to us, so feel free to ask us anything, anytime. You can also schedule a free-of-cost consultation regarding your needs with one of our professionals, and also get a quote ready at the earliest.
Key Responsibilities: Research and Analysis: Conduct experiments to study microorganisms (bacteria, viruses, fungi, etc.) in controlled laboratory settings. Investigate the interactions between microorganisms and human/animal/plant systems. Perform genetic, biochemical, and microbiological analyses of samples. Develop methods for isolating, identifying, and cultivating microorganisms. Data Collection and Interpretation: Analyze results from microbiological tests and research to identify patterns and implications. Maintain accurate records of research findings, including laboratory notes, test results, and statistical data. Utilize advanced software and technologies for data analysis and interpretation. Microbial Culture and Identification: Grow and maintain microbial cultures under various conditions (e.g., temperature, pH, salinity) to identify new strains or pathogens. Prepare culture media and reagents for microbiological experiments. Use microscopes, petri dishes, and other lab equipment to study microorganisms. Quality Control and Safety Compliance: Ensure compliance with safety standards and laboratory protocols, particularly in handling pathogenic microorganisms. Develop and implement quality control measures to ensure the accuracy and reliability of test results. Supervise laboratory technicians and assistants. Reporting and Documentation: Prepare detailed reports and research papers for publication in scientific journals or internal use. Communicate findings to colleagues, clients, or stakeholders through presentations and meetings. Assist in the preparation of grants and funding proposals for future research projects. Collaboration: Work with other scientists, clinicians, or regulatory bodies to contribute to broader scientific initiatives or public health goals. Provide technical advice on microbiological issues to other departments, organizations, or public health agencies. Skills and Qualifications: Education : Bachelor's degree in Microbiology, Biology, or a related field (entry-level). Master's or Ph.D. in Microbiology or a specialized field may be required for advanced positions. Technical Skills : Strong understanding of microbiological laboratory techniques, including culturing, staining, and microscopy. Proficiency in using laboratory equipment (e.g., autoclaves, PCR machines, spectrophotometers). Familiarity with data analysis software (e.g., SPSS, R, Microsoft Excel). Job Types: Full-time, Permanent, Fresher Pay: ₹25,465.78 - ₹40,040.66 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
The responsibilities for this position include monitoring clinical trials to ensure adherence to protocols and regulations, conducting site visits to verify data accuracy and compliance, assisting in patient recruitment and ensuring informed consent procedures, maintaining trial documentation, reporting findings to stakeholders, and ensuring proper handling and storage of investigational drugs. Additionally, collaborating with investigators, sponsors, and regulatory authorities is a key aspect of this role. Key skills required for this position include attention to detail to ensure accuracy in trial data and documentation, regulatory knowledge with an understanding of GCP, FDA, and ICH guidelines, effective communication skills for interaction with research teams and sponsors, problem-solving abilities to address challenges in trial execution, and project management skills for coordinating multiple aspects of clinical studies. This is a full-time position with benefits such as health insurance and Provident Fund offered. The work schedule is during day shifts and the work location is in person.,
About the job: Key Responsibilities: Assist in recruitment and onboarding processes Maintain employee records and HR documentation Coordinate training programs and workshops Track training attendance and effectiveness Support HR initiatives and employee engagement activities Liaise with trainers, vendors, and departments for training needs Who can apply: Only those candidates can apply who: Salary: ₹ 2,00,000 - 2,50,000 /year Experience: 0 year(s) Deadline: 2025-08-28 23:59:59 Skills required: MS-Office About Company: Here at Refined Reports Data, we take pride in our champion customer support team. Ensuring customer satisfaction is of utmost importance to us, so feel free to ask us anything, anytime. You can also schedule a free-of-cost consultation regarding your needs with one of our professionals, and also get a quote ready at the earliest.