Gita Masand
Supervisor Clinical Trial Manager-clinical Studies @UT MD Anderson
Signup · Get unlimited contacts
WORK HISTORY
Supervisor Clinical Trial Manager-clinical Studies @UT MD Anderson
Houston, TX, US
Lead, manage clinical research teams while conducting multiple clinical research trials- study notes documentation, adherence to need of the research study, serving as liaison to patients, study team and inpatient teams, CROs, sponsorsManaging complex trials and completing regulatory forms (SAE forms, Continuing review, Informed consents, reporting mandatory IRB reports for unexpected events etc)Responsible for the development/amendment of clinical study documents, including documents such as study protocols, informed consent forms (ICFs), and regulatory filesLead clinical trial research protocols workflow - clinical trial templates (CCTs) for EHR system (EPIC), reviewing coverage analysis (CAs) reports to evaluate the financial budget for the prospective clinical trials, reviewing Investigator-initiated research agreement, Material transfer agreements.Well-versed with different databases- Bioclinica CTMS, Medidata RAVE EDC, REDCAP, Interactive Web Response System (IWRS), Kite clinical.
EDUCATION
Jiwaji University
Ph.D, Chemistry
ABOUT GITA MASAND
CCRP-certified Clinical trial professional | Experience biomedical professional with 10+ years in basic and clinical research and management | Proven record in effectively handling multiple clinical projects with quality results | Experience Liaison between clinical site and study sponsors with interpersonal and decision making skills| Strong understanding of Good Clinical Practices (GCP), Standard Operating Procedures (SOPs), Clinical research budget and finance (CRF)| Excellent leadership and communication skills with ability to work in diverse environment and personnel|
This profile is compiled from publicly available professional sources. Unifers is not affiliated with or endorsed by LinkedIn. Request removal of this profile.