Clinical Research Job Vacancies 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.

we have hiring the candidates who are experience in field sale and in insurance field minimum 1 years of experience

Position: Clinical Research CoordinatorQualification Bio Science (B.Pharm/Bio Tech etc.)Experience Above 1 Year (Clinical Research Experience must) Timing General ShiftSalary 2L 2.5L (Per annum)Location Visakhapatnam/Chennai/BangaloreLanguage Know English/Kannada/TeluguJOB Description Clinical Research Coordinator To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Coordinate between the local/Central laboratory and courier for the shipment. Assist the pharmacist in drug accountability and temperature maintaining logs. Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report Sr.DGM daily and take advice for further action.

A clinical applications specialist educates and trains healthcare professionals to use new software and equipment like radiation apparatuses, imaging equipment and medical management software in hospital settings or other healthcare facilities.As a CAS you often perform product and device demonstrations or install new software and computer programs and train staff on how to use them leading workshops and seminars for the equipment or softwareThe primary duties and responsibilities of a CAS working with vendors and healthcare facilities include Evaluating and testing software vendors and systems Selecting the right program match for an organization and implementing it Delivering customer service and training throughout the implementation process Preparing all elements of the transition to new devices or software Troubleshooting, maintaining and optimizing the software Monitoring the transition process and reporting updates to senior managers Establishing relationships within the medical field to advance sales Collect feedback on site and system usage data (post-market survey testimonials case studies...) Available for frequent travel to Centers as per the requirements.QualificationsMinimum Requirements At least 3 yrs of Experience as an Application Specialist Biomedical engineer degree or equivalent bachelors degree in information science engineering or computer science. Command of written and spoken English proficiencySpecialized Knowledge and Skills Technology Skill Problem-Solving skill Communication and Customer Service Skill Flexibility Knowledge of Patient care Knowledge of medical imaging CT and MRI hand-on Experience will be Add-onPlease send your resume

Openings for Medical Summary Associates in BTM LayoutMedical Summary AssociateGreetings from Shri Misri Solutions Private Limited!Roles and Responsibilities:Read, examine, identify treatment records, progress notes, and other documentation related to specific medical conditions listed by claimants ensuring accuracy, completeness, specificity, and appropriateness of diagnosis information.Act as a detective to identify any evidence within claimant files that provide any history or evidence to support a medical claim.Familiarity with Windows Operating System, MS Office, Web browsers, Skype, Acrobat Reader, Google Docs, etc.Should possess very good knowledge of language of medicine, human anatomy and physiology, and pharmacology.Required Experience, Skills and QualificationsEligibility: Life Science Graduates / Post Graduates, B.A.M.S, B.H.MS., B.D.S with relevant experience in US Healthcare and exposure to medical records reviews. Experienced Medical Transcription Professionals (more than 10 years), Experienced Medical Coding Professionals (more than 7 years), Experienced Medical Summary Associates.Any other qualification pertaining to Medical Industry. Relevant experience (medical record reviewing / examining, abstracting, or summarizing). Immediate joiners, ready to be interviewed at Bangalore will be given preference.Selection Process Initial resume screening, Skill and domain screening (medical terminology and record reviewing) Personal interview.Remuneration:32000-39000 CTC. Per monthShift:Day shift, office based only.No Walk-inNumber of vacancies: 5Location:Shri Misri Solutions Private LimitedNo. 18,1st Floor, 100ft.Road, 1st Phase,BTM Layout 2nd Stage, Bangalore-560076.Landmark: Above, THE KARNATAKA STATE CO-OPERATIVE APEX BANK LIMITED.Job Type: Full-time (Permanent)Key Skills: Medical Summary Associates, M

Department: Medical Communications Content search, writing and editing of several types of documents such as review articles, manuscripts, product monographs, newsletters, case reports, training manuals/slides, CME slide deck, journal summaries, etc Proficient writing and communication skills with flawless English language proficiency, presenting the research data to target audience in a reader friendly manner. In-depth knowledge of various therapeutic areas. Knowledge of relevant guidelines related to structure and contents of specific document with good understanding of Vancouver style of referencing. Familiar with searching medical literature databases such as PubMed, ResearchGate, DeepDive, etc. Perform quality assurance checks on edited manuscripts to ensure that they meet the standards of international publications Provide timely feedback to our editors, manage deadlines, ensure high quality standards and able to furnish primary proofed documents. Delivery of projects/tasks within the given/agreed timelines. Adherence to processes, scientific code of conduct and ethics of writing (reference backed writing and no plagiarism).

Job Openings for 15 Agency Development Manager Jobs with minimum 2 Years Experience in JP Nagar, Bangalore,Koramangala, Bangalore, having Educational qualification of : Professional Degree, B.A, B.C.A, B.Com, M.B.A/PGDM, M.Com with Good knowledge in Clinical Research etc.