Clinical Research Fresher Jobs in Bangalore

Review medical records and translate them into standardized codes using ICD-10, CPT, and HCPCS coding systems. Collaborate with healthcare providers to obtain accurate information for coding purposes. Ensure all codes are compliant with healthcare regulations and insurance requirements. Assist in maintaining accurate documentation and coding practices to meet healthcare standards. Communicate with the coding and billing departments to resolve discrepancies or issues. Stay updated with changes in medical coding practices and healthcare regulations. Educational Background: Nursing degree (RN, LPN, or related nursing qualifications). Certification (Preferred, but not required): Certification in Medical Coding (e.g., CPC, CCS) or willingness to pursue certification after employment. Technical Skills: Basic knowledge of medical terminology, anatomy.Why Join Us? Training & Development: Comprehensive Medical Coding training will be provided to help you gain expertise in medical coding. Career Growth: We offer opportunities for career advancement and professional development within the healthcare industry. Work-Life Balance: Flexible working hours and a supportive environment. Competitive Compensation & Benefits: Health insurance, paid time off, and other benefitsQualificationsPharmacy : B.Pharmacy / M.Pharmacy / Pharmd Life Sciences : Microbiology,Biotechnology Biochemistry Botany zoology chemistry BioInformatics Medical : MBBS BDSParamedical : BHMS BAMS GNM ANM Nursing MLT Food and Nutrition

About Clinogenesis Research Institute:Clinogenesis Research Institute is a premier training and research organization dedicated to advancing careers in clinical research, bioinformatics, and life sciences. With a focus on providing comprehensive training and career support, we work closely with industry partners to ensure that our students and interns gain relevant experience and are well-prepared for career success.Position Overview:We are seeking motivated and detail-oriented Clinical Research Interns to join our team. This role provides a unique opportunity to gain hands-on experience in clinical research while working alongside experienced professionals. Interns will assist in various stages of clinical trials, data collection, and analysis, gaining essential skills in research practices and regulatory compliance.Responsibilities:Assist in the design, planning, and execution of clinical trials and research projects.Collect, review, and organize clinical data from research studies.Support data entry, verification, and ensure data quality and compliance with regulatory standards.Coordinate with cross-functional teams, including data management, biostatistics, and medical affairs.Prepare documentation, reports, and presentations for project updates and regulatory submissions.Maintain accurate study documentation and ensure adherence to GCP (Good Clinical Practice) and ethical guidelines.Qualifications:Currently pursuing or recently completed a degree in life sciences, clinical research, biostatistics, pharmacy, or a related field.Strong analytical skills and attention to detail.Ability to work effectively in a team-oriented environment.Proficiency in MS Office applications (Excel, Word, PowerPoint).Knowledge of GCP, ICH guidelines, and basic clinical trial processes is a plus.Excellent written and verbal communication skills.