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Clinical Research

Clinical Research. Importance of resume. Resume. The first impression And maybe the last too…. Resume reflects. Your commitment to good documentation (a key requirement for CR) Your academic background Your work experience

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Clinical Research

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  1. Clinical Research Importance of resume

  2. Resume The first impression And maybe the last too….

  3. Resume reflects • Your commitment to good documentation (a key requirement for CR) • Your academic background • Your work experience • Your constant endeavor to stay updated (in the form of trainings, courses, workshops etc)

  4. Parts of Resume • Initial description in 2-3 lines • Academic Background • Professional Experience • Key Responsibilities and Achievements • Trainings • Personal Information

  5. Job responsibilities and Achievements • Clearly mention each responsibility • If separate responsibilities in two diif organizations, to be mentioned separately • Achievements to be highlighted ( as italics / parenthesis/underline) • E.g

  6. CRA: responsibilities • Responsible for SOP identification or development • Responsible for which all activities during the study: site selection, initiation, monitoring close-out, Investigational Product managemement, central lab handling, etc • Handled how many sites during the trial • Prepared monitoring reports for submission to sponsor

  7. CRA: Achievements • Handled site initiation independently • Fastest recruiting sites • Least no. of data clarification forms (DCFs) generated by data management for his sites • Multiple therapeutic areas

  8. PM: responsibilities • Responsible for budgeting, recruiting CRAs • Responsible to deliver within pre-defined time lines • Responsible for telecons, face-to-face interaction with sponsor • Managing the CRAs and Clinical Trial Assistant (CTAs)

  9. PM: Achievements • Project completed before time • All sites actively recruiting • Handled different therapeutic areas • Managed trials for different sponsors • Received recommendations from Sponsors • Part of global clinical trials for US FDA/ EU submissions

  10. Medical Monitor: Responsibilities • Part of site initiation team • Actively looks into subject inclusion criteria before a subject is recruited in the study • Visits the site for Medical Monitoring • Manages Serious Adverse Event • Submitted SAE reports to regulatory authorities

  11. Medical Monitor: Achievements • All SAEs managed within timelines • All subjects recruited as per protocol

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