Summary
Overview
Work History
Education
Skills
Timeline
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Larnie Morrison

Melbourne,VIC

Summary

25 years of experience in the Research Industry has been an incredible journey both professionally and personally. I started my professional journey as a research nurse at the Royal Children's Hospital in Melbourne working on a very successful Rotavirus Clinical Trial. My role progressed to a Study Coordinator at the Austin Hospital Stroke Foundation and then a natural progression to a Study Monitor then Study Manager and now to my current role as a Senior Site Relationship Manager. My skills and knowledge are varied, working in site facing roles within the hospital, to working with pharmaceutical companies and clinical research organisations.

My leadership within all of my positions has allowed me to play a critical role in driving success and growth in all areas of research.

Overview

10
10
years of professional experience

Work History

Senior Site Relationship Manager

Bristol Myers Squibb
01.2020 - Current


  • Developing, managing and maintaining interface and long-term relationships with clinical sites for several outsourced studies and ensuring a harmonized approach to site management with studies run in-house. Building and enhancing the image and reputation of the company with sites locally and providing an interface between the company, the investigator and Partner CROs to create an optimal environment for clinical trials, enabling timely and high quality output.
  • Building and managing clinical site relationships (investigators, site staff, Key Opinion Leaders ) for local, regional and global programs across different Therapeutic Areas that have been outsourced to a CRO Partner.
  • Act as liaison between the company, CRO Partner and investigational sites building overall investigator and site staff awareness in order to develop the image and reputation of the company.
  • Provide close collaboration with Partner CRO and the support of internal stakeholders such as Vendor Operations Manager, Medical Affairs, Research Clinical Collaboration and local development leads in the Asian Pacific Region.

Senior Site Monitor

Bristol Myers Squibb
01.2015 - 01.2020
  • Reduce downtime on projects by troubleshooting issues quickly and efficiently, resulting in faster completion times.
  • Overseeing the conduct of clinical trials at investigational sites, ensuring data quality and compliance, and maintaining effective relationships with site personnel.
  • Ensuring clinical trials are conducted in accordance with the study protocol, applicable regulations, and standard operating procedures.
  • Participating in site feasibilities, site selection, initiation and close out visits.
  • Assessing the site's capabilities, resources, and compliance with regulatory requirements. Training site staff, and ensuring all necessary documentation are in place.
  • Conducting regular monitoring visits to clinical trial sites to monitor the progress of the study. Reviewing and verifying source documents, case report forms, and other trial-related documents to ensure data accuracy and integrity.
  • Ensuring that the trial is conducted in compliance with the protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • Collecting and reviewing data from the clinical trial sites. Ensuring data is collected accurately, completely, and in a timely manner. Assisting sites in resolving data queries and discrepancies.
  • Generating monitoring reports and communicating findings to the study team and site personnel.
  • Ensuring that the clinical trial sites adhere to quality standards, regulatory requirements, and ethical guidelines. Identifying and addressing any compliance issues or deviations from the protocol.
  • Participating in internal and external audits to ensure data integrity and regulatory compliance.
  • Establishing and maintaining effective relationships with site personnel, investigators, and study coordinators. Providing support, guidance, and training to site staff as needed. Serving as the primary point of contact for site-related issues and facilitate communication between the site and the study team.

Senior Clinical Research Associate

INC Research
02.2015 - 11.2015
  • Overseeing the conduct of clinical trials at investigational sites, ensuring data quality and compliance, and maintaining effective relationships with site personnel.

Site Manager

INC Research
02.2014 - 02.2015
  • Overseeing and managing clinical trial operations at investigational sites, ensuring compliance, data quality, and effective relationships with site personnel. Playing a crucial role in ensuring the successful execution of clinical trials in accordance with regulatory requirements and the company's standard operating procedures.


Education

Bachelor of Science - Nursing

Australian Catholic University
Melbourne, VIC
12.1992

Associate of Applied Science - Nursing

Australian Catholic University
Ballarat, VIC
12.1991

Skills

  • Relationship Building
  • Client Relationships
  • Relationship building and management
  • Excellent Communication

Timeline

Senior Site Relationship Manager

Bristol Myers Squibb
01.2020 - Current

Senior Clinical Research Associate

INC Research
02.2015 - 11.2015

Senior Site Monitor

Bristol Myers Squibb
01.2015 - 01.2020

Site Manager

INC Research
02.2014 - 02.2015

Bachelor of Science - Nursing

Australian Catholic University

Associate of Applied Science - Nursing

Australian Catholic University

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Larnie Morrison