Handymen - Working specialties
Experience:
Clinical research associate
Performed site activities including site initiation, sites selection, Site monitoring and site closeout visits.
ICF and source data verification.
Follow-up with subject recruitment.
Follow-up with site during SAE procedures, query resolutions in eCRF.
Collection and review of Essential documents.
Support TMF setup & maintenance.
Ability to perform all Clinical trail monitoring activities independently.
Management of Clinical trail supply.
Writing visit reports, filing, and collecting trail documentation and reports.
To liaise with other departments within the organization for the timely Achievement of related milestones.
Trial methodologies
Investigator Meetings
Completing regulatory documents
Subject Tracking tools
Coordinating site operations
Patient Recruitment
Data Collection
Project Monitoring
Education:
Pharma D ( Doctor of pharmacy)
Skills:
Project Monitoring
Excellent interpersonal skills as well as verbal and spoken communication skills.
Adapt to the situation which makes me and the people with me feel comfortable with each other.
Patient Assessment
Taking Vital Signs
Patient Care
Recording Patient Medical History
Record-Keeping
Medicine Administration
Blood Pressure Monitoring
Glucose Checks
MS Office (Word, Excel, PPT)
Language skills:
English
Hindi
Additionally:
I have good communication in clinical research, pharmacist and clinical pharmacist