Download - Clinical Research Importance of resume. Resume The first impression And maybe the last too…
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 Your constant endeavor to stay updated (in
the form of trainings, courses, workshops etc)
Parts of Resume
Initial description in 2-3 lines Academic Background Professional Experience Key Responsibilities and Achievements Trainings Personal Information
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
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
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
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)
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
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
Medical Monitor: Achievements
All SAEs managed within timelines All subjects recruited as per protocol