Array ( [0] => clinical-trials [1] => hyderabad ) Clinical Trials Jobs in Hyderabad,Clinical Trials Job Vacancies in Hyderabad Telangana
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Clinical Trials Job Vacancies in Hyderabad

Hiring Fresher - Medical Coder - Hyderabad/Bangalore/Mumbai

Medi Infotech

Medical Coding Trainee Clinical Research Pharmacovigilance Bpharma Pharmacology Pharmacist Chemistry Biotechnology Biochemistry Clinical Trials Nursing Nurse BDS Dentist Bhms Bhms Graduate Medical LAB Technician Microbiology Bioinformatics BPT Bsc Nursing Zoology Botany Biotech Zoology Medical Transcription
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
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Senior Statistical Programmer

Tk-Chain

SDTM ADAM TLF CDISC CRF FSP Clinical Trials Statistical Programmer Work From Home
Company: TK-Chain Location: Hyderabad, ChennaiExperience: 5+Job Overview: We are seeking a dedicated Senior Statistical Programmer to join our dynamic team. You will be responsible for the development, quality control, and documentation of statistical (SAS) programming deliverables for clinical research studies.Key Responsibilities:1. Lead and oversee the development of SAS programs for the management and statistical analysis of clinical trial data.2. Develop, test, and validate statistical tables, listings, and graphs (TLGs) in support of the statistical analysis plan.3. Support the generation and review of protocols, data management plans, study reports, and other regulatory documents.4. Provide input to the statistical analysis plan, table shells, data integration plans, and mock-ups.5. Ensure data quality by designing and validating key data checks and listings.6. Develop specifications for derived datasets and perform data transformation as necessary.7. Collaborate effectively with data management and biostatistics teams, clinicians, and other project stakeholders.8. Guide junior programmers and provide mentoring as needed.9. Keep abreast of new developments in SAS programming and clinical research, and act as a subject matter expert for the team.Required Qualifications and Skills:1. Bachelor's or masters degree in Statistics, Mathematics, Computer Science, or a related field.2. Minimum of 3 plus years of statistical programming experience in the pharmaceutical, biotech, or CRO industry.3. Excellent SAS programming skills and proficiency in SAS/Base, SAS/Macro, SAS/Graph, and SAS/STAT.4. Familiarity with CDISC SDTM and Adam data standards.5. In-depth understanding of clinical trial data and extremely complex statistical methods.6. Excellent problem-solving skills and a proactive approach to identifying and resolving issues.7. Strong written and verbal communication skills, with the ability to translate complex data into
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Clinical Programmer

Worldcare clinical

  • 2 - 8 yrs
  • 19.0 Lac/Yr
  • Banjara Hills Hyderabad
Clinical Programming Clinical Trials Industry Computer Science Preferred.
Primary responsibilities are clinical programming and data analysis; understanding various data sources and coding programs to extract data into analysis-ready data sets; creation of software test plans and testing, and development of statistical analysis reports. Data analysis includes descriptive analysis of Independent Reader performance and other metrics to assess the quality of services offered by WCC. Clinical Programmer works closely with Project Managers, Software Developers and Clients regarding data quality and data transfers.Essential Functions Lead clinical programming aspects of WCC clinical trials, including consulting with external statistical consultants. Analyze existing and new programs, processes and databases to identify and/or guide implementation of modifications aimed at increasing workflow efficiency. Develop SAS databases, when applicable Review and assure the quality, integrity, accuracy, and completeness of clinical trial data based on project specific guidelines. Develop and implement quality review of data using SAS data validation programs. Standardize datasets to ensure compliance with data transfer requirements and enhance usability. Develop programs and guide efforts to perform robust data manipulation and error detection to ensure data integrity. Extract data from the WCC trial system and provide analytical reporting. Review data exports and reports to identify, investigate and reconcile data discrepancies with Clinical Operations staff and/or clients Data Managers. Implement variability testing criteria to monitor Independent Reader performance. Author and review Data Transfer Files specifications (DTF) for incoming and outgoing data files. Respond to client requests for additional data and/or data analysis, as needed. Collaborate effectively and build productive relationships within across the global operations team. Performs other job-related duties as assigned.
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Drug Safety Scientist

NITZ Consulting Private limited

  • 5 - 10 yrs
  • 20.0 Lac/Yr
  • Hyderabad
Pharmacovigilance Expert Clinical Researcher Clinical Trials Drug Safety Scientist Work From Home
Quality review of ICSRs, surveillance of known or emerging safety issues, participation in an escalation process, risk evaluation, and analysis of safety data. Apply safety concepts and regulations contained within FDA CFR, ICH, and EU GVP to management of Safety data across the development life cycle. Analyze aggregate safety data within a clinical program towards tracking and trending of risk assessments and additional mitigation measures. Contributes to safety sections of the investigational new drug and new drug applications, investigator or regulator communications, Investigator brochure, and other reports (DSUR) Participates in the set-up and maintenance of adverse event processes in global clinical trials Ensure Quality of the Individual Case Safety Report, including data and a concise, medically relevant narrative.
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