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Clinical Data Manager (Freshers) Hyderabad

Komal Enterprise

  • Fresher
  • 4.8 Lac/Yr
  • Humayun Nagar Hyderabad
Data Cleaning Data Reconciliation Database Programming Electronic Data Capture Clinical Data Management Data Standards Data Analysis Database Design Regulatory Compliance SAS Programming Medical Coding Cdisc Standards Quality Control Data Collection Protocol Development Clinical Trials Data Validation Data Review Data Entry Data Reporting
We are seeking a Clinical Data Manager to join our team. This is a part-time, work-from-home position, ideal for freshers who have completed their 10th grade education. nnKey Responsibilities:n- Data Collection: Gather and organize clinical data from various sources to ensure accuracy and completeness.n- Data Management: Maintain and update databases, ensuring the information is consistently accurate and accessible.n- Quality Assurance: Perform regular checks on data to identify discrepancies or errors and implement solutions to enhance data quality.nnRequired Skills and Expectations:nCandidates should be detail-oriented and able to work independently while managing their time effectively. Strong organizational skills are necessary to handle multiple tasks and ensure deadlines are met. Good communication skills will be important for collaborating with team members and understanding instructions clearly. A keen interest in the clinical research field will be beneficial. nnThis position is suitable for individuals who are eager to learn and develop their skills in clinical data management while working flexibly from the comfort of their homes. A proactive attitude and willingness to adapt to new technologies and processes will enhance your success in this role.
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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
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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.
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Clinical Data Management

Croissance Clinical Research

  • 1 - 2 yrs
  • Miyapur Hyderabad
Clinical Research Clinical Operations Client Coordination Case Report Form Data Entry 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.
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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.
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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.
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