1059 Biochemistry Jobs - Page 2

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Priya 9600450980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Rubini-9600405840 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

Job description: Eligibility Criteria: Designation: Trainee Medical Coder Qualification: B.Pharma & M.Pharma (No Standing Arrears) Should have 60% in all the academics Work From Office only Work Location: Kochi, Kerala Shift: Day Age limit: 28 Yrs Salary: As Per Industry Interested Candidates share your resume durgadevi.chandrasekaran@corrohealth.com Durga HR 8248059972

Role Definition: The Laboratory Director, heading the Center of Excellence (COE) in Laboratory Medicine, is responsible for the strategic and operational leadership of all laboratory medicine services, including Clinical Pathology, Hematology, and Biochemistry. The role ensures business enablement, diagnostic accuracy, quality assurance, operational efficiency, clinician engagement, and technical team development. It involves high-level expert consultation, end-to-end laboratory operations management, adherence to regulatory and NABL/ISO standards, and strategic collaboration with clinicians and healthcare providers to strengthen market leadership. Role Deliverables: Business Enablement Drive scientific and commercial growth of laboratory medicine services. Diagnostic Accuracy & TAT Adherence Ensure 100% accurate and clinically correlated reporting within committed turnaround times. Laboratory Operations Management Oversee Central and Regional Labs for optimal efficiency, cost control, and resource management. Helpdesk Management Ensure seamless resolution of clinician and branch queries with technical authority. Clinician Engagement & Scientific Consultation Build scientific credibility and strengthen clinician partnerships. Quality Management & Compliance Achieve and maintain NABL/ISO compliance with robust internal and external quality programs. People Leadership Build, mentor, and lead high-performing technical teams with a strong performance and learning culture. Task and Activities: Business Enablement: Drive revenue growth through strategic business development initiatives. Collaborate with business teams to enhance partnerships with hospitals, clinics, and healthcare providers. Act as a medical advisor to key clinicians and healthcare institutions. Engage in scientific marketing, RTMs, CMEs, industry events, and expert consultation to expand diagnostic services. Provide high-level consultation to referring physicians and healthcare professionals to enhance patient management. Respond to technical queries, critical value discussions, and interpretation requests from doctors. Collaborate with business development to address technical queries from partner hospitals and doctors. Collaborate with Marketing for CME content, diagnostic bulletins, and clinician awareness programs. Assess the relevance and volume of current test panels; recommend test menu enhancements based on market and medical needs. Diagnostic Accuracy & TAT Adherence Monitor end-to-end sample workflows for Biochemistry, Hematology, Immunology, and Clinical Pathology. Personally validate critical reports and ensure proper clinical correlation before release. Conduct daily delta checks, histogram reviews, and trend analysis for critical parameters. Identify bottlenecks and ensure 99%+ TAT adherence, coordinating with logistics and operations teams Laboratory Operations Management: Implement the laboratory policies, procedures, and quality control protocols as aligned with the Medical Directorate. Oversee daily operations of Central and Regional Laboratories, ensuring efficiency, cost-effectiveness, and compliance. Ensure the accuracy of diagnostic tests and reports. Manage the laboratory resources, including equipment, reagents and other supplies. Manage the laboratory s financials, including budgeting and cost control. Monitor financial performance indicators and implement corrective actions as needed Quality Management and Compliance: Conduct daily quality management practices across Central and Regional Laboratories to meet regulatory requirements. Ensure daily internal QC, EQAS, and LIMS-based control validations are completed and signed off. Manage the Internal audits and participate in external quality assurance programs to ensure compliance. Monitor delta checks, critical value communication, and compliance with QC protocols Implement corrective and preventive actions (CAPA) based on audit findings and quality assessments. Ensure SOPs, checklists, and dashboards are updated on real time basis. Coordinate with the QC Team to monitor and enhance quality control measures. Report quality indicators trends in monthly meetings and track improvements Helpdesk Management: Lead the Laboratory Helpdesk team and serve as the primary point of contact for resolving technical queries from branches and clinicians. Ensure seamless communication and issue resolution within defined SLAs. Manage escalations related to test results, patient concerns, and clinician inquiries. Develop and implement protocols to handle service-related complaints effectively. People Leadership: Recruit, train, and supervise technical teams. Set an individual role clarity, roster with each team member aligned with the laboratory objectives. Conduct daily huddles with the team to discuss ongoing activities and address any issues. Hold weekly meetings with the team to discuss operational performance indicators and lead measures. Conduct monthly 1:1 meetings with direct repartees to review progress on KPIs and plan the way ahead. Document and share feedback with each team member. Assess individual ASK (Attitude, Skills, Knowledge) on a quarterly basis and manage the learning of the team in collaboration with the HR team to enhance skills and drive career paths. Monthly recognize and reward high performance and initiate improvement plans where necessary. Achieve the People Score of 90. Success Metrics: 100% achievement of strategic goals (Revenue & Profitability) 100% accuracy rate in diagnostic tests and reports. 100% timely delivery of diagnostic results within established turnaround times 90% achievement of Quality indicators Adhere to a budget with no more than 2% variance. Customer feedback score of 4.8 or higher. Monthly RTM/ CME/ Clinician engagement activity as per calendar 100% compliance in NABL audits, IQC, EQAS Requirements :: D/DNB in Pathology, with additional training/fellowship in Hematopathology or Laboratory Medicine preferred. 12 15 years of post-MD experience, including 5+ years in leadership of multi-specialty diagnostic labs with NABL/ISO audit exposure. Proficiency in Clinical Pathology, Hematology, Biochemistry, LIMS, quality protocols (IQC/EQAS), and advanced diagnostic technologies. Strong clinician engagement, team mentoring, strategic decision-making, and business-aligned diagnostic leadership.

We are looking for a highly skilled and experienced MD Dermatologist Consultant Doctor to join our team at Skinfinity Derma Clinic. The ideal candidate will have 2-7 years of experience in dermatology. Roles and Responsibility Conduct thorough medical examinations and diagnose various skin conditions. Develop and implement effective treatment plans for patients with different skin conditions. Perform surgical procedures, such as biopsies and excisions, as needed. Provide guidance on preventive measures to minimize the risk of skin cancer and other diseases. Collaborate with other healthcare professionals to ensure comprehensive patient care. Stay updated with the latest developments in dermatology through continuous learning and professional development. Job Requirements Hold an MD degree in Dermatology from a recognized institution. Possess strong knowledge of dermatological procedures and treatments. Demonstrate excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment and prioritize tasks is essential. Strong analytical and problem-solving skills are required. Commitment to providing high-quality patient care and maintaining confidentiality.

Responsibilities: * Conduct biochemistry, biotech, biomedical tests with IVD equipment * Prepare samples for ELISA assays and RT-PCR analysis * Ensure quality control through documentation and QA processes

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols. Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

The Senior Analyst position in Food at our company in Chinsura, Hooghly is a full-time on-site role where you will be responsible for conducting chemical and instrumental analysis of food products. Your duties will include developing, verifying, and validating analytical methods, as well as maintaining laboratory equipment. Ensuring compliance with regulatory standards, preparing detailed reports, and collaborating with team members for accurate and timely processing of samples will also be part of your role. We are seeking candidates with expertise in chemical and instrumental analysis of food products, experience in method development and validation, and proficiency in maintaining laboratory equipment while ensuring regulatory compliance. Strong skills in report preparation, data analysis, problem-solving, and critical thinking are essential. Additionally, the ideal candidate should possess team handling skills, in-depth knowledge of FSSAI rules and regulations, attention to detail, and the ability to work both independently and collaboratively. A minimum of 4-5 years of experience in an NABL accredited food testing laboratory is mandatory for this role. A Master's degree in Food Science, Food and Nutrition, Chemistry, or Biochemistry is also required. If you meet these qualifications and are looking for a challenging opportunity in the food industry, we encourage you to apply for this position.,

You are a detail-oriented and dedicated Junior Lab Technician with 6 months to 2 years of experience in Biochemistry, Clinical Pathology, and Hematology, as well as exposure to Elisa technique. Your role involves performing routine diagnostic tests, conducting Elisa-based tests, processing samples accurately, maintaining lab equipment, preparing reagents, and ensuring quality control procedures are followed. You will be responsible for recording and reporting test results accurately, following safety protocols, managing inventory, and supporting senior staff in daily lab functions. To qualify for this position, you need a Diploma/Degree in Medical Laboratory Technology (DMLT/BMLT or equivalent), familiarity with lab equipment, attention to detail, and the ability to follow technical instructions. Strong communication and team collaboration skills are essential, along with a willingness to work in shift-based schedules. Experience in a manual testing environment, handling high sample volumes, and exposure to quality assurance and NABL documentation are preferred. This is a full-time, permanent position with benefits including health insurance, life insurance, and provident fund. The schedule may involve day, evening, night, or rotational shifts, with performance and yearly bonuses offered. You must be willing to commute or relocate to Gurugram, Haryana before starting work. Overall, you will play a crucial role in the laboratory services department by assisting in diagnostic tests, sample processing, and maintaining quality standards.,

p style="text-align:justify"> Oakridge Gachibowli is a premium international day school in India. We have the proud privilege of being the pioneers of IB schooling in South India and one of the largest providers of IB education in India. We have 150+ IB-trained teachers with years of experience, helping us consistently achieve outstanding results and seeing our students go on to study at some of the world s leading universities. Oakridge offers IB, CBSE, and Cambridge curricula, and is recognized as one of the best schools in Hyderabad, India. . Job Description Please write the Job Description. Job Responsibilities

Manager, Regulatory Affairs - CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Primary responsibilities include, but are not limited to: Regulatory Responsibilities: Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills: Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 7 yrs of Industry Pharmaceutical industry experience out of 4 years experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Applied Engineering, Biochemistry, Business Processes, Chemical Engineering, Communication, Communication Management, Compliance Investigations, Documentation Standards, Electronic Common Technical Document (eCTD), Employee Training Programs, Global Regulatory Submissions, Immunoassays, Immunochemistry, Management Process, Microbiology, Molecular Biology, Molecular Microbiology, Pharmaceutical Manufacturing, Policy Implementation, Records Retention Management, Regulatory Affairs Compliance, Regulatory CMC, Regulatory Communications {+ 4 more} Preferred Skills: Job Posting End Date: 07/26/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Looking for an experienced Senior Lab Technician skilled in Biochemistry, Microbiology, Hematology & Serology. Must be proficient in diagnostic procedures, QC protocols, equipment handling & lab documentation. Minimum 5 yrs exp. is required Required Candidate profile Educational Requirement : B.Sc MLT / (DMLT) Diploma in Medical Laboratory Technology Interested Candidates Drop CVs to HR Himani WhatsApp: +91 73079 60780 Mail: hr@accurislabs.com

Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (JRF) in a time bound research project for a temporary period, purely on contractual basis in School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India.as per the following details. Position Junior Research Fellow (JRF) Number of Vacancy One Project Title MULTIFUNCTIONAL SILICA COMPOSITE COATINGS ON TI-6AL-4V BY SPIN COATING AND IT’S OPTIMAL IMPLANT/SCAFFOLD FABRICATION FOR BIOMEDICAL APPLICATIONS Sponsoring agency Council of Scientific & Industrial Research (CSIR) CSIR-ASPIRE 01WS(030)/2023-24/EMR-II/ASPIRE Department Department of Chemistry, School of Advanced Sciences (SAS) Project Tenure 3 years Job Description Project aims to develop the usability of defect free coatings and nanofibous scaffolds of bioactive silica glass and it’s composite for biomedical applications. Knowledge about ceramic materials, coatings and corrosion knowledge is required. Strong communication and writing skills are desirable. Essential Qualification Integrated BS-MS/MSc, M.Sc in material science, chemistry, physics, M Tech in nanotechnology or equivalent degree, with 55% marks and with valid NET/GATE test. Upper Age Limit JRF-28Yrs. Age relaxation The upper age limit is relaxable up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates. Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m. Principal Investigator Dr. U. Vijayalakshmi Professor (Grade I) Department of Chemistry, School of Advanced Sciences (SAS), Vellore Institute of Technology, Vellore Tamil Nadu – 632014 Send your resume along with relevant documents pertaining to the details of qualifications, GATE/NET score card, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (10/08/2025) through online http://careers.vit.ac.in Please note that the CV should include contact details (address, mobile phone no., email ID), date of birth, qualifications mentioned clearly. Complete information regarding publications of research papers in SCOPUS Indexed Journals should be mentioned in the CV. Incomplete applications will be rejected. No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the Department of Physics, School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “Development of cost-efficient and scalable perovskite based colloidal nanoparticles for high performance plastic scintillators” Qualification : M.Sc./ M.Tech. in Physics/ Materials Science or related fields from recognized universities/institutes with a minimum of first class and with GATE / CSIR-UGC JRF / NET-LS qualification. Mandatory Skills : Candidates should have a strong research background in synthesis and characterization of nanomaterials. Experience with colloidal semiconductor nanomaterials and related photo physics is desirable. Stipend : Rs. 37,000 p.m. + 8% HRA for the first two years (JRF); Rs. 42,000 p.m.+ 8% HRA for the third year (SRF) will be as per Institute norms. No. of Vacancies : 01 Post (ONE) Age Limit (if any) : Not exceeding 30 years i.e. Age must be from 18 to 30 years Sponsoring Agency : ANRF, PMECRG program, New Delhi, India Duration : 36 Months Principal Investigator : Dr. Abhinav Anand, Assi stant Professor, Department of Physics School of Advanced Sciences, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Interested candidates with the above-mentioned qualifications can send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 18/08/2025) through the website: http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Position- Pathology Technician Experience- 1-15 years Qualification- BMLT + DMLT (Mandatory) Location- Jamshedpur Skills- Biochemistry/ Hematology/ Immuno- Analyzers / Routine Clinical Pathology / Microbiology Share your CV- 9777017652

As a postdoctoral fellow in Professor Ashim Rai's lab at Ahmedabad University, you will be conducting experimental research focused on the biophysics of Salmonella-host cytoskeleton interactions. The research project aims to uncover the molecular mimicry mechanisms employed by Salmonella pathogenic factors to manipulate host cell cytoskeletal networks. Your role will involve designing and executing experiments using interdisciplinary approaches such as reconstitution biology, fluorescence spectroscopy, and DNA nanotechnology. Proficiency in fluorescence microscopy and spectroscopy is essential for this position. Your responsibilities will include designing and conducting experiments in cytoskeletal research, analyzing a diverse range of experimental data, preparing manuscripts for publication, writing grants for research funding, and mentoring PhD and undergraduate students. You will be expected to leverage your expertise in protein expression and purification using bacterial and insect cell systems, as well as your experience in time-lapse fluorescence imaging and the use of a fluorescence spectrophotometer. The ideal candidate for this role should hold a PhD degree in Biochemistry or Biophysics with a strong publication record in high-impact peer-reviewed journals. Prior experience in cytoskeletal biology would be advantageous. Ahmedabad University is committed to providing a research-driven and project-based learning environment within the Division of Biological and Life Sciences. If you are a motivated and self-driven individual with a passion for biophysics research, we encourage you to apply for this exciting opportunity. Please submit your CV and cover letter to Professor Ashim Rai via email at ashim.rai@ahduni.edu.in. Duration of the position: 36 months.,

Responsibilities: * Conduct lab tests using Hematology, Microbiology, Molecular Biology techniques with expertise in RT-PCR, Serology, ELISA. * Prepare samples for analysis and record results accurately. Annual bonus Provident fund

Key Responsibilities Drive sales of laboratory products, particularly microbiology and chromatography items, including HPLC/GC vials and columns. Build and maintain strong relationships with clients across the assigned territory. Conduct regular client visits to follow up on leads and ensure order closures. Consistently improve sales performance by nurturing both existing accounts and identifying new business opportunities. Travel extensively within Telangana to engage with customers and ensure satisfaction. Lead and mentor a team of field sales executives, providing direction and support. Track team performance, coach team members, and help achieve set sales targets. Work closely with senior management to plan and execute region-specific sales strategies. Desired Skills & Attributes Demonstrated ability to lead and manage sales teams effectively Strong interpersonal and communication skills A proactive and self-driven sales approach Capability to plan strategically and execute sales initiatives Flexibility and readiness to travel as required within the region Preferred Background: Experience with distribution networks or laboratory product sales will be an added advantage. Educational Qualifications B.Sc / M.Sc in Life Sciences (Microbiology, Biochemistry, Biotechnology, Chemistry) B.Pharm / M.Pharm / Pharm.D

Oakridge International School is looking for Lab. Assistant to join our dynamic team and embark on a rewarding career journey Prepare and set up laboratory equipment and materials for experiments and tests Collect and process samples according to established protocols Conduct routine laboratory tests and procedures, such as preparing solutions, conducting experiments, and performing assays Record and maintain accurate data and records of results Operate laboratory equipment, such as centrifuges and microscopes, and maintain equipment in good working condition Follow established protocols and regulations, including safety guidelines and quality control procedures Maintain a clean and organized laboratory environment, including ordering and stocking supplies Communicate with laboratory supervisors and other team members to provide updates and ask questions Strong technical skills, attention to detail, and the ability to follow precise instructions Good organizational and communication skills

Key Responsibilities: Analytical Method Development & Validation Develop and validate robust HPLC methods for characterization and quantification of biological products (e.g., monoclonal antibodies, recombinant proteins). Perform method optimization, robustness studies, and transfer protocols as per ICH guidelines. Routine & Stability Testing Conduct analysis of in-process, release, and stability samples using: HPLC/UPLC Capillary and Gel Electrophoresis UV spectrophotometric methods Host Cell DNA quantification (e.g., qPCR-based methods) HCP ELISA and other immunoassays Instrument Operation & Maintenance Perform routine maintenance, calibration, and troubleshooting of analytical instruments including HPLC, electrophoresis systems, spectrophotometers, and ELISA readers. Ensure timely qualification and performance verification of instruments. Documentation & Compliance Prepare and review SOPs, STPs, protocols, reports, and analytical records in compliance with regulatory requirements. Maintain accurate and complete documentation in laboratory notebooks and electronic systems. Quality & Regulatory Compliance Participate in internal and external audits, and support regulatory submissions with analytical data. Cross-functional Collaboration Work closely with R&D, Quality Control, and Regulatory Affairs teams to support product development and lifecycle management. Provide technical support during investigations, deviations, and CAPAs. Training & Development Train junior analysts and new team members on analytical techniques and laboratory practices. Stay updated with advancements in analytical technologies and regulatory expectations. Qualifications & Experience: M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or related life sciences discipline. 4 8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA based techniques. Familiarity with regulatory guidelines (ICH, FDA, EMA) and quality systems. Key Skills: Strong analytical and problem-solving skills Attention to detail and data integrity Excellent documentation and communication abilities Proficiency in software tools like Empower, Chromeleon, SoftMax Pro, etc. Ability to manage multiple projects and meet deadlines

Job Desription Medical Coding provides tremendous opportunities to all talented life science and paramedical graduates who have passion for Healthcare Industry.Medical coding is amongst the most in demand profession in India,USA,Philippine,UAE Develop a complete understanding of the Medical management Procedures. Perform medical review assessment (MRA) on utilization of health services (eg healthcare plans, workers compensation products etc) in an accurate, efficient and timely manner while ensuring compliance with utilization management regulations and adherence to state and federal mandates. Provide succinct negotiable points based on the submitted medical records that identify necessary medical treatment, casually related care, response or lack of response to treatment, etc. Identify missing records and information that are necessary in the completion of the medical review assessment. Adhere to federal, state, URAC, client, and established MediCall best practice WCUM time frames, as appropriate. This Role is Open to Fresh Graduates with Excellent English Communication Skills. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments maintains a Working Knowledge of Cpt-4, Icd-10-cm, and Icd-10-pcs Coding Principles, Governmental Regulations, Uhdds (uniform Hospital Discharge Data Set) Guidelines, Aha Coding Clinic Updates, and Third-party Requirements Regarding Coding and Documentation Guidelines HR BHAVANI 9566284629

Kamineni academy of medical sciences is looking for Assistant Professor - Anatomy to join our dynamic team and embark on a rewarding career journey Teach a range of courses in the department, at both the undergraduate and graduate levels Conduct original research in the field and publish findings in academic journals and at conferences Advise students and mentor junior faculty members Participate in department and university-wide committees, such as curriculum committees and search committees Pursue external funding opportunities to support research and teaching activities Engage in professional development activities to stay current in the field and enhance teaching skills

Kamineni academy of medical sciences is looking for Associate Professor - Anatomy to join our dynamic team and embark on a rewarding career journey Teaching and Instruction: Associate Professors are responsible for teaching undergraduate and/or graduate-level courses in their area of expertise They develop syllabi, prepare course materials, deliver lectures, facilitate discussions, and assess student performance They may also supervise student research projects, theses, and dissertations Research and Scholarship: Associate Professors engage in research activities, pursue scholarly publications, and contribute to the advancement of knowledge in their field They conduct research projects, secure research funding, collaborate with colleagues, and publish their findings in academic journals or present them at conferences They may also mentor and guide graduate students in their research pursuits Academic Advising: Associate Professors provide academic guidance and advising to students They assist students in selecting courses, developing academic plans, and pursuing research or career opportunities within their discipline They may also serve as thesis advisors or mentors to graduate students Service and Committee Work: Associate Professors contribute to the administrative functions of their department, college, or university through service and committee work They participate in faculty meetings, serve on academic committees, contribute to curriculum development, and provide input on various institutional matters

Immediate requirement of MD Biochemistryy Assistant professor/Associate/Professor for various Medical colleges in India.Attractive Salary and accommodation.

Immediate requirement of MD Anatomy, physiology Biochemistryy Assistant professor/Associate/Professor for various Medical colleges in India. Attractive Salary and accommodation. Onroll Also available