Freshers Can Apply. Coordinate training program ( Medical Coding CPC, ICD-10, CPT, HCPCS), Student counseling and recruitment. (Good Communication in English/Malayalam ) 1.Typically 0-1 or more years experience in student recruitment/counseling . 2. Bachelors degree in Science is an added advantage. 3. Good Computer Knowledge. Email/ Drafting Letters [Excellent Skills] 4. Good Communication and Presentation Skills. 5. Ability to work as part of a team and without close supervision. 6. Ability to work under pressure and meet timelines. 7.Marketing experience is an added advantage Job Type: Full-time Pay: ₹9,844.00 - ₹30,194.00 per month Schedule: Day shift Supplemental Pay: Commission pay Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred) Counselling: 1 year (Preferred)
As a fresher in the field of research and regulatory affairs, you will be responsible for completing appropriate role-specific training to perform job duties. Under supervision, you will assist in various administrative tasks to support team members in project execution. This may include running system reports, maintaining meeting minutes, preparing and distributing status reports, creating and managing study documents, and more. Your role will also involve updating and maintaining systems within project timelines and per project plans. Ensuring the accuracy and completeness of source documents, CRFs, Investigator Site File, and other study-related documents according to ICH-GCP guidelines will be crucial. Additionally, you will be responsible for completing the eCRF and maintaining Investigational Product integrity based on specific temperature requirements. Furthermore, you will play a vital role in preparing for site qualification visits, initiation visits, monitoring visits, and site close-out visits. Organizing ethics committee meetings, completing review forms, and submitting all study-related documents to EC will also be part of your duties. You may need to coordinate with local and central labs, assist in Safety Reporting within required timelines, contribute to patient selection and recruitment processes, and support the Informed Consent Process. To excel in this position, you should possess basic knowledge of applicable research and regulatory requirements such as ICH GCP and relevant local laws, regulations, and guidelines. Proficiency in MS Applications like Microsoft Word, Excel, and PowerPoint is essential. Strong written and verbal communication skills in English, effective time management abilities, and a results-oriented approach to work delivery will be critical for success. Moreover, you should be capable of establishing and maintaining effective working relationships with coworkers, managers, and clients. Strong listening and phone skills, as well as good data entry abilities, are also required to fulfill the responsibilities of this role. Candidates from the years 2016 to 2019 with educational backgrounds in B.Tech, M.Tech (Biotechnology), MSc (Biotechnology, Microbiology, Biochemistry), B.Pharm, M.Pharm, Pharm D, MSc, and BSc (Life Science: Bioinformatics, Biomedical Engineering, etc.) are encouraged to apply for this position. This job is suitable for individuals who can work from Monday to Friday at the specified in-person work location.,
TRAINING PROVIDED FOR FRESHERS Review and assign appropriate codes for both Hospital billed services Ensure accuracy of ICD-10-CM, CPT, HCPCS , and modifier usage per payer guidelines Evaluate and resolve claim denials, including medical necessity and timely filing issues Provide feedback on payer denials and assist with the appeal process when appropriate Reference and interpret UB04, CMS-1500, EOBs , and RAs to support coding validation Collaborate with internal teams and external partners to resolve coding discrepancies Maintain up-to-date knowledge of industry standards, payer-specific rules, and coding regulations Work independently and maintain productivity standards in an onsite setting Use electronic health record (EHR) systems and documentation tools to access and update coding information Refer to written training resources and coding references as needed T TRAINING WILL BE PROVIDED FOR FRESHERS Certified Billing and Coding Specialist (CBCS) or AAPC Coder Certification or Training will be provided Strong knowledge of ICD-10-CM, CPT, HCPCS, UB04 , and CMS-1500 forms Familiarity with Medicare, Medicaid, HMOs, PPOs , and managed care plan guidelines Proficient in medical terminology, healthcare documentation, and coding best practices Strong comprehension, problem-solving, and conflict resolution skills Excellent verbal and written communication skills in English Ability to work independently with minimal supervision Preferred Skills: Experience working in a fully remote coding or RCM environment Prior involvement in denial resolution and payer appeals Comfortable using multiple healthcare platforms and EHR systems Ability to analyze coding patterns and identify billing trends Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Education: Bachelor's (Preferred) Work Location: In person
TRAINING PROVIDED FOR FRESHERS Review and assign appropriate codes for both Hospital billed services Ensure accuracy of ICD-10-CM, CPT, HCPCS , and modifier usage per payer guidelines Evaluate and resolve claim denials, including medical necessity and timely filing issues Provide feedback on payer denials and assist with the appeal process when appropriate Reference and interpret UB04, CMS-1500, EOBs , and RAs to support coding validation Collaborate with internal teams and external partners to resolve coding discrepancies Maintain up-to-date knowledge of industry standards, payer-specific rules, and coding regulations Work independently and maintain productivity standards in an onsite setting Use electronic health record (EHR) systems and documentation tools to access and update coding information Refer to written training resources and coding references as needed T TRAINING WILL BE PROVIDED FOR FRESHERS Certified Billing and Coding Specialist (CBCS) or AAPC Coder Certification or Training will be provided Strong knowledge of ICD-10-CM, CPT, HCPCS, UB04 , and CMS-1500 forms Familiarity with Medicare, Medicaid, HMOs, PPOs , and managed care plan guidelines Proficient in medical terminology, healthcare documentation, and coding best practices Strong comprehension, problem-solving, and conflict resolution skills Excellent verbal and written communication skills in English Ability to work independently with minimal supervision Preferred Skills: Experience working in a fully remote coding or RCM environment Prior involvement in denial resolution and payer appeals Comfortable using multiple healthcare platforms and EHR systems Ability to analyze coding patterns and identify billing trends Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Education: Bachelor's (Preferred) Work Location: In person
The role involves coordinating study activities and timelines, scheduling participant visits, and ensuring compliance with regulatory requirements. You will be responsible for coordinating study procedures such as laboratory tests and imaging studies. You will support the analysis of research data, including statistical analysis and interpretation of study findings. Additionally, you will assist in the preparation of study-related documentation, research protocols, informed consent forms, and regulatory submissions. Ensuring compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and institutional policies is a crucial part of the role. This includes maintaining study documentation, conducting internal audits, and participating in regulatory inspections when necessary. Collaboration with interdisciplinary teams is essential for the smooth conduct of clinical research studies. You will work closely with physicians, nurses, laboratory personnel, and statisticians. Communication of study progress and findings to stakeholders such as investigators, sponsors, and regulatory agencies is also part of the role. Participation in ongoing training and educational activities related to clinical research is expected. This includes protocol-specific training, GCP training, and professional development opportunities. Upholding ethical standards in the conduct of clinical research is paramount. This includes protecting the rights and welfare of research participants and maintaining the confidentiality of study data. The ideal candidate should have a BDS, MSc in Biotechnology, Microbiology, Biochemistry, B. Pharm, M. Pharm, Pharm D, MSc, BSc in Life Science, Bioinformatics, Biomedical Engineering, etc. Freshers with up to 1 year of experience are preferred for this role. This is a full-time position located in Kochi, Kerala. The work schedule is in the morning shift. The education requirement is a Master's degree. The job type is Fresher/Internship.,