Research & Administration Professional

Overview

Looking for part-time work (4 hours/day)

at $7.63/hour ($727.27/month)

B.S. Tourism - 4 year course

Last Active

July 27th, 2014 (4340 days ago)

Member Since

July 27th, 2014

Profile Description

I am Lily Flor P. Alejandro, previously, I worked for 2 years as Site Start Up Specialist for Quintiles Philippines Inc. And spent the past 15 years working as Research Admnistrator for MSD Philippines.
In my current capacity, I am responsible to Create and prepare the clinical study budget. Ensure that initial budget discussion before the investigators’ meeting and final budget agreement signed by the investigators before the drug supplies are sent to the site. Ensure timely payment to the investigator and study staff. Create, update and reconcile study budgets utilizing MRL Grants and Consultant System (MGCS). Track budgets, payments and liquidation, and reconcile with the study budget agreements. Prepares copies of protocol for distribution to potential investigators; in behalf of CRO makes necessary visits / telephone contacts to follow-up interest of MDs in participating in the study. Secures ALL pre-study approvals according to international strategic time frames. Prepares regulatory documents for Clinical Trial Certificate (CTC) application. Responsible for seuring responses (from CRA/CRM/MD) and preparing final reply to any queries BFAD consultants may pose prior to granting approval or disapproval of CTC.
Follows-up with Regulatory Team the approval of CTC application. In behalf of the principal investigator, prepares documents essential for application to Ethics Review Boards (ERB). Responsible for securing responses and preparing final reply to queries that may be posed by (ERB) member prior to granting of approval / disapproval to ERB application. Facilitates translation of patient informed consent (ICF). Prepares pre-study documents, secures appropriate signatures and submits to MRL or CDSP. Keeping minutes of the meeting, Receives non-clinical study supplies. Process telephone and fax messages for the team and Arranged Flight Schedules for the clinical team.
I am highly-organized as evidenced by the findings in the Clinical Research Audit conducted every year.
I have good planning skills, all projects and budget allocation and spending are implemented and track in a timely manner.
I am results-oriented as I have always managed to ensure the completion of data from clinical studies.
My consistent interaction with our internal and external clinical research stakeholders has honed my interpersonal and technical skills that make me effective on the job.