As a pharmacologist, you'll need to: design, plan and conduct controlled experiments and/or clinical trials to improve understanding of a drug's activity collect, analyse and interpret data using computers, high technology measuring systems and other sophisticated equipment make recommendations based on research findings apply and develop the results of research to work through a variety of applications, such as new products, processes, techniques and practices draw up proposals for future developmental tests organise and oversee tests of new drugs and medicines, ensure quality control and secure approval for their use liaise with regulatory authorities to ensure compliance with local, national and international regulations plan, coordinate and supervise the duties of other technical staff and train or mentor early-career pharmacologists. Job Types: Full-time, Permanent, Fresher Pay: ₹23,000.00 - ₹70,000.00 per month Benefits: Health insurance Provident Fund Work from home Schedule: Day shift Evening shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Work Location: On the road
Job Brief: We’re looking for Microbiologist to join our team and help us develop new ways to detect and treat disease. Microbiologist Duties: Perform routine and complex laboratory tasks Obtain and analyze results, performing analyses such as bacteriology, bacteriology, and virology Perform quality control duties Assist in the development of interpretive protocols, policies and procedures Liaise with physicians and staff in order to assist with diagnosis and treatment Perform routine functions associated with the prevention and control of workplace hazards and communicable diseases Perform routine and more complex laboratory procedures Assist with quality control procedures and laboratory quality assurance Perform routine and more complex laboratory procedures Apply the oral and written communication skills necessary for working in a team environment Conduct quality control procedures for microbiological products Assist in the development of interpretive protocols, policies and procedures Perform routine functions associated with the prevention and control of workplace hazards and communicable diseases Obtain and analyze results, performing analyses such as bacteriology, bacteriology, and virology Perform quality control Microbiologist Responsibilities: Associate’s degree from an accredited college or university in microbiology, biology, or related field 3+ years’ experience in a microbiology laboratory, with specialization in environmental microbiology Knowledge of laboratory techniques and equipment Knowledge of microbiology principles and practices Knowledge of environmental health and safety laws Job Types: Full-time, Permanent, Fresher Pay: ₹28,000.00 - ₹65,000.00 per month Benefits: Health insurance Provident Fund Work from home Schedule: Day shift Fixed shift Supplemental Pay: Commission pay Performance bonus Yearly bonus Work Location: In person
Medical Coder responsibilities and duties The responsibilities and duties section is the most important part of the job description. Here you should outline the functions this position will perform on a regular basis, how the job functions within the organization and the title of the manager the person will report to. Comply with all legal requirements regarding coding procedures and practices Conduct audits and coding reviews to ensure all documentation is accurate and precise Assign and sequence all codes for services rendered Collaborate with billing department to ensure all bills are satisfied in a timely manner Communicate with insurance companies about coding errors and disputes Submit statistical data for analysis and research by other departments Contact physicians and other health care professionals with questions about treatments or diagnostic tests given to patients with regard to coding procedures Job Type: Full-time Pay: ₹18,000.00 - ₹38,000.00 per month Benefits: Internet reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Work Location: On the road
Medical Coder responsibilities and duties The responsibilities and duties section is the most important part of the job description. Here you should outline the functions this position will perform on a regular basis, how the job functions within the organization and the title of the manager the person will report to. Comply with all legal requirements regarding coding procedures and practices Conduct audits and coding reviews to ensure all documentation is accurate and precise Assign and sequence all codes for services rendered Collaborate with billing department to ensure all bills are satisfied in a timely manner Communicate with insurance companies about coding errors and disputes Submit statistical data for analysis and research by other departments Contact physicians and other health care professionals with questions about treatments or diagnostic tests given to patients with regard to coding procedures Job Type: Full-time Pay: ₹18,000.00 - ₹38,000.00 per month Benefits: Internet reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Work Location: On the road
Key duties Site management : Conduct site visits and monitor trial progress. Monitoring : Ensure data accuracy, integrity, and compliance. Regulatory compliance : Adhere to legal and GCP standards. Patient safety : Track and report adverse events. Documentation : Maintain study records and case report forms. Liaison : Communicate between sponsors, sites, and investigators. Job Type: Full-time Pay: ₹20,000.00 - ₹45,000.00 per month Benefits: Health insurance Internet reimbursement Schedule: Day shift Work Location: On the road
Key duties Adverse event reporting : Collect, evaluate, and report adverse drug reactions (ADRs). Data entry : Input and maintain safety data in databases. Regulatory compliance : Ensure compliance with drug safety regulations. Safety signal detection : Identify and assess potential safety risks. Documentation : Prepare and review safety-related reports. Collaboration : Work with clinical, medical, and regulatory teams on safety issues. Job Type: Full-time Pay: ₹450,000.00 - ₹800,000.00 per year Benefits: Health insurance Internet reimbursement Schedule: Day shift Work Location: On the road
Key Responsibilities: Data Collection & Validation: Review and clean data from clinical trials, ensuring compliance with regulatory standards. Database Management: Oversee the setup, maintenance, and quality control of clinical trial databases. Data Review: Ensure data is accurate, complete, and meets protocol requirements. Collaboration: Work closely with clinical operations, biostatistics, and project management teams. Documentation & Reporting: Maintain proper documentation and provide regular updates on data status. Compliance: Ensure adherence to Good Clinical Practice (GCP), FDA regulations, and other industry standards. Job Type: Full-time Pay: ₹500,000.00 - ₹950,000.00 per year Benefits: Health insurance Internet reimbursement Schedule: Day shift Work Location: On the road
Key duties Regulatory Submissions : Preparing and submitting documents for product approvals to regulatory agencies (e.g., FDA, EMA). Compliance : Ensuring that products meet regulatory standards across various markets (e.g., labeling, testing, safety). Documentation Management : Maintaining regulatory files, certificates, and approvals. Cross-functional Collaboration : Working with R&D, legal, quality assurance, and marketing teams to ensure compliance at all stages. Regulatory Updates : Keeping track of regulatory changes and advising the organization on necessary adjustments. Audit Support : Assisting with audits and inspections by regulatory bodies. Job Type: Full-time Pay: ₹20,000.00 - ₹45,000.00 per month Benefits: Health insurance Internet reimbursement Schedule: Day shift Work Location: On the road
A Clinical Research Coordinator is responsible for a variety of duties including the following: Overseeing the trouble-free running of clinical trials Collecting data obtained from research, coding and analyzing it Managing budgets set aside for research Communicating with participants regarding study objectives Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules Liaising with laboratories regarding research findings Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines Directing the collection, labeling, storage and transport of all specimens Making sure that all equipment and supplies needed for the study are in-stock and in good working order Job Types: Full-time, Permanent, Fresher Pay: ₹25,000.00 - ₹49,000.00 per month Benefits: Health insurance Provident Fund Work from home Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus
Job description Correspond or meet with providers to resolve abusive billing practices and to reach an appropriate financial settlement Educate providers on plan policies and guidelines, medical necessity criteria, UM programs correct billing methods and procedure codes by written and verbal communication Audit documentation to ensure it supports complete, accurate and compliant billing with both CMS and payer requirements Assist practice physician and mangers with all coding errors, denials, or issues encountered in the billing process Monitor charge review queues to ensure that all accounts flow through to billing appropriately Submit all charges into billing system for claims processing Act as liaison between billing company and the Perinatal Unit Codes billing supplies and implants Job Type: Full-time Pay: ₹14,371.89 - ₹34,067.15 per month Schedule: Day shift
A Clinical Research Coordinator is responsible for a variety of duties including the following: Overseeing the trouble-free running of clinical trials Collecting data obtained from research, coding and analyzing it Managing budgets set aside for research Communicating with participants regarding study objectives Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules Liaising with laboratories regarding research findings Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines Directing the collection, labeling, storage and transport of all specimens Making sure that all equipment and supplies needed for the study are in-stock and in good working order Job Types: Full-time, Permanent, Fresher Pay: ₹25,000.00 - ₹49,000.00 per month Benefits: Health insurance Provident Fund Work from home Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus
A Clinical Research Coordinator is responsible for overseeing the trouble-free running of clinical trials, collecting data obtained from research, coding, and analyzing it. They manage budgets set aside for research and communicate with participants regarding study objectives. Administering questionnaires and monitoring participants to ensure they adhere to the study's rules is also part of their duties. The Coordinator liaises with laboratories regarding research findings and monitors the study to ensure it complies with protocols, is ethically-conducted, and follows regulatory standards. They are responsible for maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines. Directing the collection, labeling, storage, and transport of all specimens is also a key responsibility. The Coordinator ensures that all equipment and supplies needed for the study are in-stock and in good working order. This role may include job types such as Full-time, Permanent, and Fresher. The benefits offered may include Health insurance, Provident Fund, and Work from home options. The schedule may involve Day shift and Morning shift timings. Additionally, there may be performance bonuses and yearly bonuses associated with this position.,
Responsibilities for drug safety associate Assist with additional Drug Safety Specialist and/or Medical Operations Leader (MOL) activities as required Perform literature searches Review and process serious adverse events, spontaneously reported adverse drug reactions and/or other medically related information per assigned tasks and study specific procedures, serving as a technical expert with regard to all aspects of safety monitoring Assist the MSS Functional Lead (eg Serve as support to the Medical & Safety Services management in all aspects, including coordinating interdepartmental activities (eg Bachelor's degree, or higher in nursing or pharmacy, healthcare professionals preferably Excellent oral, written and interpersonal communication skills, with writing expertise in the scientific or medical field highly preferred Demonstrable strong organizational and time management skills with the ability to triage and manage multiple responsibilities with a high degree of self-motivation and accountability Experience in cardiovascular therapeutic area preferred Qualifications for drug safety associate Ability to follow guidelines and procedural documents (experience of working with SOPs ) is preferred Knowledge or experience with Excel, PowerPoint, Visio is preferred Pharmacy qualification or other healthcare related degree or equivalent F drug safety experience in a pharmaceutical company Excellent oral and written communication skills, interpersonal skills and cultural awareness Job Types: Full-time, Permanent, Fresher Pay: ₹30,092.95 - ₹52,058.83 per month Benefits: Health insurance Paid sick time Provident Fund
As a candidate for this position, you will be expected to have a strong foundation in higher level science courses, particularly anatomy and physiology, with a focus on pursuing a career in healthcare at a graduate or doctorate level. Your prior experience in healthcare settings, especially in the role of a medical scribe, will be highly valued for this role. You should possess a deep knowledge of medical terminology and an understanding of medical note content, as well as medical billing and coding procedures. Your responsibilities will include taking notes and accurately documenting them in the electronic health records system during patient visits. Additionally, you will be required to learn about medical procedures and collaborate with a team to supervise and document patient care. In this role, you will be responsible for completing and submitting medical records with the guidance of a supervising physician or doctor. It is essential to maintain professional communication with patients and supervising physicians at all times. Furthermore, you should be proficient in handling administrative procedures and providing assistance to the physician in administering tests and medicines. This is a full-time position with benefits that include internet reimbursement, a day shift schedule, and the opportunity for performance bonuses. The work location for this role may vary and may involve being on the road as needed.,
Medical Coder Responsibilities: Extracting relevant information from patient records. Liaising with physicians and other parties to clarify information. Examining documents for missing information. Ensuring documents are grammatically correct and free from typing errors. Performing chart audits. Advising and training physicians and staff on medical coding. Informing supervisor of issues with equipment and computer program. Ensuring compliance with medical coding policies and guidelines. Medical Coder Requirements: High school diploma, GED, or suitable equivalent. Proficient computer skills. Excellent communication skills, both verbal and written. Strong people skills. Outstanding organizational skills. Ability to maintain the confidentiality of information. Job Types: Full-time, Permanent, Fresher Pay: ₹30,965.98 - ₹45,489.06 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries. Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis. Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations. Responsible for organizing and preparing for both internal and external auditing and study monitoring visits. Coordination and management of clinical trials, including communication with Sponsors and regulatory authorities. Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved. Interact with study participants as directed/required by the protocol and/or study team. May be responsible for tissue sample work. Job Type: Full-time Pay: ₹25,500.00 - ₹38,000.00 per month Benefits: Internet reimbursement Ability to commute/relocate: Ahmadabad District, Gujarat: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred) Work Location: In person
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries. Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis. Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations. Responsible for organizing and preparing for both internal and external auditing and study monitoring visits. Coordination and management of clinical trials, including communication with Sponsors and regulatory authorities. Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved. Interact with study participants as directed/required by the protocol and/or study team. May be responsible for tissue sample work. Job Type: Full-time Pay: ₹25,500.00 - ₹38,000.00 per month Benefits: Internet reimbursement Ability to commute/relocate: Ahmadabad District, Gujarat: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred) Work Location: In person
As a Microbiologist at our company, you will be responsible for performing routine and complex laboratory tasks, obtaining and analyzing results in areas such as bacteriology and virology, and assisting in the development of interpretive protocols, policies, and procedures. Your role will also involve liaising with physicians and staff to aid in diagnosis and treatment, as well as conducting quality control procedures for microbiological products. Additionally, you will be expected to apply your oral and written communication skills effectively in a team environment. Key Responsibilities: - Perform routine and complex laboratory tasks - Obtain and analyze results in areas such as bacteriology and virology - Assist in the development of interpretive protocols, policies, and procedures - Liaise with physicians and staff for diagnosis and treatment support - Conduct quality control procedures for microbiological products Qualifications Required: - Associates degree in microbiology, biology, or related field from an accredited college or university - 3+ years of experience in a microbiology laboratory with a specialization in environmental microbiology - Knowledge of laboratory techniques, equipment, microbiology principles, and practices - Familiarity with environmental health and safety laws In addition to the above responsibilities and qualifications, the job also offers benefits such as health insurance, provident fund, work from home option, day shift or fixed shift schedules, performance bonus, and yearly bonus. The work location is in person. Please note that this is a full-time, permanent position with opportunities for fresher candidates.,
As a Medical Coder, your role involves extracting relevant information from patient records, liaising with physicians and other parties for information clarification, examining documents for missing data, ensuring grammatical correctness and error-free typing in documents, conducting chart audits, providing guidance and training to physicians and staff on medical coding, reporting equipment and computer program issues to your supervisor, and upholding compliance with medical coding policies and guidelines. Key Responsibilities: - Extract relevant information from patient records - Liaise with physicians and other parties to clarify information - Examine documents for missing information - Ensure grammatical correctness and typing error-free documents - Perform chart audits - Advise and train physicians and staff on medical coding - Inform supervisor of equipment and computer program issues - Ensure compliance with medical coding policies and guidelines Qualifications Required: - High school diploma, GED, or suitable equivalent - Proficient computer skills - Excellent communication skills, both verbal and written - Strong people skills - Outstanding organizational skills - Ability to maintain the confidentiality of information The company offers benefits such as health insurance, paid sick time, and Provident Fund. The job type is Full-time, Permanent, and suitable for Fresher candidates. The work location is in person.,
Job Brief: We’re looking for Microbiologist to join our team and help us develop new ways to detect and treat disease. Microbiologist Duties: Perform routine and complex laboratory tasks Obtain and analyze results, performing analyses such as bacteriology, bacteriology, and virology Perform quality control duties Assist in the development of interpretive protocols, policies and procedures Liaise with physicians and staff in order to assist with diagnosis and treatment Perform routine functions associated with the prevention and control of workplace hazards and communicable diseases Perform routine and more complex laboratory procedures Assist with quality control procedures and laboratory quality assurance Perform routine and more complex laboratory procedures Apply the oral and written communication skills necessary for working in a team environment Conduct quality control procedures for microbiological products Assist in the development of interpretive protocols, policies and procedures Perform routine functions associated with the prevention and control of workplace hazards and communicable diseases Obtain and analyze results, performing analyses such as bacteriology, bacteriology, and virology Perform quality control Microbiologist Responsibilities: Associate’s degree from an accredited college or university in microbiology, biology, or related field Knowledge of laboratory techniques and equipment Knowledge of microbiology principles and practices Knowledge of environmental health and safety laws Job Types: Full-time, Permanent, Fresher Pay: ₹28,000.00 - ₹65,000.00 per month Benefits: Health insurance Provident Fund Work from home Work Location: In person