TRUSTED BY
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As an experienced Life Science Executive and Founder/CEO of a small CRO, I have scaled organizations and led teams to develop innovative solutions for companies and patients. I apply my practical experience navigating the intricacies of clinical trial planning combined with deep expertise and a passion for technology to attain significant achievements.
Customized solutions based on your specific challenges.
Support C-Level teams on strategic issues including execution of CDPs, protocol development, site ID strategies, implementation of technology, and outsourcing strategies.
Provide executive-level oversight for projects or programs, including clinical operations, data management, statistical programming, and medical writing.
Support the selection, configuration, and implementation of effective GCP-compliant technology solutions for clinical projects.
Develop and implement risk management solutions, protocol feasibility, site selection, startup processes, and technology implementation.
Serve in interim C-Level positions focusing on meeting significant milestones, resource allocation, and strategic management to facilitate clinical development.
TYPICAL ENGAGEMENTS INCLUDE
"Greg’s expertise and strategic insights have been instrumental in advancing our drug development programs, consistently delivering outstanding results, and guiding us through complex data and clinical challenges."
Board Director, Global Pharmaceutical Organization (Oncology Detection/Endocrinology)
“We have worked with Greg for many years and have relied on him to help develop support programs for our clinical initiatives. He has been a tremendous resource in the development and execution of our clinical trials and our overall clinical strategy.”
Senior Manager, Clinical Affairs, Global MedTech
"Greg’s professional and pragmatic approach to research and development continues to benefit my development programs. I trust him, he is not afraid to advise honestly, offering straight talk on challenges and risk. He is also an advocate of quality and prepared to include risk based quality as part of his solutions."
Vice President Clinical Quality Assurance, Pharma Start-up (Immunology/Wound Care)
WHAT CLIENTS SAY
*All references are available upon request. Contact me.
Publications & Interviews
Presentations
Ambra, G. (2019). Panel Speaker: Opportunities in a changing life sciences landscape. Life Sciences Collaboration.
Ambra, G. Future roles and career path opportunities for clinical data managers. Presented at the 22nd Annual DIA Conference "INTEGRATION ACROSS THE CLINICAL TRIAL CONTINUUM".
Ambra, G. Maximizing the potential of eClinical trials with implementation strategy. Presented at the 2nd Annual Clinical Trial Data Integration.
Service that lead the way to better business
I am a Pharma and Device Development Executive with 25 years of broad industry experience. I can handle and give you the best advice.
ABOUT ME
Years experience
>
25
Projects completed
>
500
Product approvals