Array ( [0] => clinical-research [1] => hyderabad ) Clinical Research Jobs in Hyderabad,Clinical Research Job Vacancies in Hyderabad Telangana
5

Clinical Research Job Vacancies in Hyderabad

filter
  • Location
  • Role
  • Functional Area
  • Qualification
  • Experience
  • Employer Type

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
View all details
Apply

Hiring For Clinical Data Manager

Croissance Clinical Research

  • 5 - 8 yrs
  • 16.0 Lac/Yr
  • Miyapur Hyderabad
Clinical Research Clinical Data Management Medidata Rave
Organizing Kick-off meetings with the client co-ordination with the functional Head. Responsible for allocating the project/Study to team members. Responsible for Review and Internal approval of Data Management Plan (DMP), Case Report Form (CRF), and Edit check Specification Document (ESD). Responsible for Review and Internal approval of Data Entry Guidelines, Self-Evident Correction Document (SEC). Internal approval of Annotated CRF (aCRF) and Functional Design Specification (FDS) Document. Responsible for preparing and training the SOPs. Responsible for approval of database screens, Edit checks designed in database and DCF/Query tracker. Internal Quality Control for all Data Management Documents like Data Management Plan, Annotated CRF, Functional Design Specification Document, and Edit check Specification Document. Responsible for Issuing the Database Test Certificate. Responsible for Database Lock and Unlock procedures. Responsible for exporting the data to SAS team for analysis. Responsible for Review and approval of Master Data Management File (MDMF). Responsible for Data Management Presentation in Investigator meeting. Providing inputs for proposal development in co-ordination with the Function Head.
View all details
Apply

Clinical Data Manager

Worldcare clinical

  • 3 - 9 yrs
  • Banjara Hills Hyderabad
Clinical Research Pharmacovigilance Clinical Operations Clintrial Clinical Data
Essential Functions Review and assure the quality, integrity, accuracy, and completeness of clinical trial data based on project specific guidelines. Develop and maintain a library of effective data quality checks. Review data exports and reports to identify, investigate, and reconcile data discrepancies with Clinical Operations staff and/or clients Data Managers. Prepare, review, and upload appropriate Data Management documents to the Trial Master File Perform thorough development testing of the datasets prior to release to production, inclusive of creating test scripts and execute testing as applicable. Author Data Transfer specifications (DTS) for incoming and outgoing data files. Collaborate effectively and build productive relationships across the global operations team. Performs other job-related duties as assignedQualifications 3+ years of data management experience in the clinical trials industry BS/BA degree or professional experience equivalent. Demonstrated successful experience in all relevant clinical data management activities in a Pharmaceutical or CRO setting. Working knowledge of clinical trial research, including FDA, GCP/ICH guidelines, GDPR, CDISC/SDTM standards and 21 CFR Part 11 Experience working with EDC systems, e.g., Medidata Rave or Oracle Inform Familiarity with industry wide coding dictionaries such as MedDRA is a plus Experience with relational databases and XML a plus Excellent written and oral communication skills. Excellent analytical and problem-solving skills Ability to function independently. Ability to prioritize and handle multiple tasks and projects concurrently
View all details
Apply

SR. CRA

ClinSync Clinical Research Pvt Ltd

  • 6 - 10 yrs
  • 10.0 Lac/Yr
  • Hyderabad
Clinical Research Associate Event Management
1.Prepare, conduct and report on activities related to the completion of site selection, initiation, routine monitoring and close-out visits2.Monitor patient enrollment to ensure recruitment targets and project timelines are met at the site and/or country level3.Perform source data verification and follow up on data queries at the site level, on-going review of any 4.Risk Based Monitoring related information influencing data quality and frequency of site visits5.Ensure accurate and timely reporting and follow up of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations6.Act as the main line of communication between the Sponsor and the site.7.Be a point of contact/liaison for in-house support services and vendors.8.Ensure proper handling, accountability and reconciliation of all Investigational Product(s) and clinical study supplies9.Review the status and contents of essential documents at the site level and reconcile study OSF/ TMF at site and/or country level.10.Experience in all types of monitoring visits.
View all details
Apply

Get Personalized Job Matches

Based on your experience, skills, interests, and career goals to help you find the most relevant opportunities faster. Register Now!

Jobs by Related Category

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.
View all details
Apply

Senior Clinical Research Associate

Croissance Clinical Research

  • 2 - 7 yrs
  • 8.0 Lac/Yr
  • Miyapur Hyderabad
Clinical Research
Dear Everyone,Today's Greetings!!We are now looking for a Senior Clinical Research Associate. The specifics are provided below.Clinical operation departmentSenior Clinical Research Associate is a job title.Experience: 27 yearsBachelor of Pharmacy/Master of PharmacySalary: According to corporate policy.Immediate joining/one month's noticeWork mode: work from officeHyderabad is the location.Local candidates are preferred.
View all details
Apply

Clinical Data Manager

Croissance Clinical Research

  • 5 - 8 yrs
  • 16.0 Lac/Yr
  • Miyapur Hyderabad
Clinical Research Clinical Data Management Medidata Rave
Organizing Kick-off meetings with the client co-ordination with the functional Head. Responsible for allocating the project/Study to team members. Responsible for Review and Internal approval of Data Management Plan (DMP), Case Report Form (CRF), and Edit check Specification Document (ESD). Responsible for Review and Internal approval of Data Entry Guidelines, Self-Evident Correction Document (SEC). Internal approval of Annotated CRF (aCRF) and Functional Design Specification (FDS) Document. Responsible for preparing and training the SOPs. Responsible for approval of database screens, Edit checks designed in database and DCF/Query tracker. Internal Quality Control for all Data Management Documents like Data Management Plan, Annotated CRF, Functional Design Specification Document, and Edit check Specification Document. Responsible for Issuing the Database Test Certificate. Responsible for Database Lock and Unlock procedures. Responsible for exporting the data to SAS team for analysis. Responsible for Review and approval of Master Data Management File (MDMF). Responsible for Data Management Presentation in Investigator meeting. Providing inputs for proposal development in co-ordination with the Function Head.
View all details
Apply

Clinical Data Management

Croissance Clinical Research

  • 2 - 4 yrs
  • Hyderabad
Clinical Research Data Management Investigator Meeting
Organizing Kick-off meetings with the client co-ordination with the functional Head. Responsible for allocating the project/Study to team members. Responsible for Review and Internal approval of Data Management Plan (DMP), Case Report Form (CRF), and Edit check Specification Document (ESD). Responsible for Review and Internal approval of Data Entry Guidelines, Self-Evident Correction Document (SEC). Internal approval of Annotated CRF (aCRF) and Functional Design Specification (FDS) Document. Responsible for preparing and training the SOPs. Responsible for approval of database screens, Edit checks designed in database and DCF/Query tracker. Internal Quality Control for all Data Management Documents like Data Management Plan, Annotated CRF, Functional Design Specification Document, and Edit check Specification Document. Responsible for Issuing the Database Test Certificate. Responsible for Database Lock and Unlock procedures. Responsible for exporting the data to SAS team for analysis. Responsible for Review and approval of Master Data Management File (MDMF). Responsible for Data Management Presentation in Investigator meeting. Providing inputs for proposal development in co-ordination with the Function Head.
View all details
Apply

Apply to 5 Clinical Research Job Vacancies in Hyderabad

  • Hyderabad Jobs
  • Ahmedabad Jobs
  • Bangalore Jobs
  • Mumbai Jobs
  • Pune Jobs
  • Chennai Jobs
  • Kolkata Jobs
  • Delhi Jobs