Summary
Overview
Work History
Education
Skills
Timeline
Generic

Subba Lakshmi Dhulipala

Cupertino,California

Summary

To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy.

Overview

1
1
year of professional experience

Work History

Clinical Research Coordinator

Stanford University, School Of Medicine
2015.04 - 2016.04
  • Collected data and followed research protocols, operations manuals, and case report form requirements.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Followed informed consent processes and maintained records.
  • Gathered, processed, and aliquoted the lab specimens.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
  • Reviewed referral information and kept track of intakes from various referral sources.
  • Developed and maintained accurate and up-to-date case report forms and source documents.
  • Maintained accurate and up-to-date case report forms and source documents for traceability.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Collected, evaluated, and modeled collected data.

Education

Certificate - Clinical Trials Design And Management (Certificate

UC Santa Cruz Extension
Santa Clara, United States
08.2012

Bachelor of Science - Molecular Biology

San Jose State University
San Jose, CA
04.2000

Skills

  • Documentation requirements
  • Good Clinical Practices
  • Study protocols
  • Specimen handling
  • Trial management
  • Participant screening
  • Research SOPs understanding
  • Specimen collections
  • Informed consent
  • Patient recruitment
  • Meeting Coordination
  • Research experience
  • Scheduling proficiency
  • Schedule Coordination
  • Data collection techniques
  • Documentation Management
  • Records Maintenance

Timeline

Clinical Research Coordinator

Stanford University, School Of Medicine
2015.04 - 2016.04

Certificate - Clinical Trials Design And Management (Certificate

UC Santa Cruz Extension

Bachelor of Science - Molecular Biology

San Jose State University
Subba Lakshmi Dhulipala