Charles Beasley charles.beasley@novotech-cro.com & | With a decade's worth of experience in the clinical research industry, I have held various roles including Regulatory Associate, Senior CRA, Clinical Lead, and Clinical Project Manager (APAC/AMEA) and Global Project Manager, Clinical Operations. I thrive in a fast-paced environment and enjoy working closely with stakeholders contributing to trial strategy and ensuring key deliverables are met seamlessly, on time, and within budget. Over the course of my Clinical Research career I have handled all phases and functional areas of clinical trials from feasibility through to close-out in a variety of therapeutic areas. I have managed Regional (APAC/AMEA) and Global Clinical Trials at CRO and Sponsor side, respectively, along with line management and Portfolio Management/Program Management responsibilities. In my current role, I serve as the Global Lead Clinical Project Manager for a 400 patient/100 site radiopharmaceutical trial in metastatic Castration Resistant Prostate Cancer (mCRPC). My Clinical Research expertise is further supported by my medical writing and regulatory submission and dossier experience, including with the FDA, EMA, TGA, Medsafe; SOP development and implementation of new systems, including CTMS/eTMF. In my spare time I enjoy keeping up to date with the latest developments in Medical Science and Clinical Research via my podcast and YouTube Channel "Good Clinical".

Charles Beasley

With a decade's worth of experience in the clinical research industry, I have held various roles including Regulatory...

Novotech, L 6, New Zealand

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Charles Beasley’s Emails [email protected]

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Charles Beasley’s Location Novotech, L 6, New Zealand

Charles Beasley’s Expertise With a decade's worth of experience in the clinical research industry, I have held various roles including Regulatory Associate, Senior CRA, Clinical Lead, and Clinical Project Manager (APAC/AMEA) and Global Project Manager, Clinical Operations. I thrive in a fast-paced environment and enjoy working closely with stakeholders contributing to trial strategy and ensuring key deliverables are met seamlessly, on time, and within budget. Over the course of my Clinical Research career I have handled all phases and functional areas of clinical trials from feasibility through to close-out in a variety of therapeutic areas. I have managed Regional (APAC/AMEA) and Global Clinical Trials at CRO and Sponsor side, respectively, along with line management and Portfolio Management/Program Management responsibilities. In my current role, I serve as the Global Lead Clinical Project Manager for a 400 patient/100 site radiopharmaceutical trial in metastatic Castration Resistant Prostate Cancer (mCRPC). My Clinical Research expertise is further supported by my medical writing and regulatory submission and dossier experience, including with the FDA, EMA, TGA, Medsafe; SOP development and implementation of new systems, including CTMS/eTMF. In my spare time I enjoy keeping up to date with the latest developments in Medical Science and Clinical Research via my podcast and YouTube Channel "Good Clinical".

Charles Beasley’s Current Industry Sapro Consulting And Cro

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Work Experience

Sapro Consulting And Cro

Strategic Partnerships Director

Thu Aug 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Telix Pharmaceuticals

Senior Clinical Project Manager

Wed May 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Aug 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time)

Telix Pharmaceuticals

Clinical Project Manager (Global Lead)

Fri Sep 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time)

Good Clinical

Director and Podcast Host

Tue Aug 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Iqvia

Regional Clinical Project Manager, AMEA (Novartis cFSP)

Thu Sep 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Sep 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)

Novotech

Project Manager

Sat May 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Aug 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Novotech

Associate Project Manager

Sun Nov 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Apr 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

Novotech

Senior Clinical Research Associate

Sun Sep 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Oct 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)

Pharmaceutical Solutions Dedicated To Excellence In Clinical Research

Senior Clinical Research Associate

Sat Jun 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Sep 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

Pharmaceutical Solutions Dedicated To Excellence In Clinical Research

Clinical Research Associate II

Thu Mar 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

Aft Pharmaceuticals

Research & Development Project Manager

Tue Nov 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Mar 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)

Aft Pharmaceuticals

Clinical and Regulatory Associate

Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Oct 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)

Lypanosys

Master's Degree Intern

Sat Jun 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)

Skills

Languages

FAQ About Charles Beasley

Charles Beasley is located at
Novotech, L 6, New Zealand

Charles Beasley is a
With a decade's worth of experience in the clinical research industry, I have held various roles including Regulatory Associate, Senior CRA, Clinical Lead, and Clinical Project Manager (APAC/AMEA) and Global Project Manager, Clinical Operations. I thrive in a fast-paced environment and enjoy working closely with stakeholders contributing to trial strategy and ensuring key deliverables are met seamlessly, on time, and within budget. Over the course of my Clinical Research career I have handled all phases and functional areas of clinical trials from feasibility through to close-out in a variety of therapeutic areas. I have managed Regional (APAC/AMEA) and Global Clinical Trials at CRO and Sponsor side, respectively, along with line management and Portfolio Management/Program Management responsibilities. In my current role, I serve as the Global Lead Clinical Project Manager for a 400 patient/100 site radiopharmaceutical trial in metastatic Castration Resistant Prostate Cancer (mCRPC). My Clinical Research expertise is further supported by my medical writing and regulatory submission and dossier experience, including with the FDA, EMA, TGA, Medsafe; SOP development and implementation of new systems, including CTMS/eTMF. In my spare time I enjoy keeping up to date with the latest developments in Medical Science and Clinical Research via my podcast and YouTube Channel "Good Clinical". Sapro Consulting And Cro

Charles Beasley currently works in the
Sapro Consulting And Cro

Charles Beasley specializes in
With a decade's worth of experience in the clinical research industry, I have held various roles including Regulatory Associate, Senior CRA, Clinical Lead, and Clinical Project Manager (APAC/AMEA) and Global Project Manager, Clinical Operations. I thrive in a fast-paced environment and enjoy working closely with stakeholders contributing to trial strategy and ensuring key deliverables are met seamlessly, on time, and within budget. Over the course of my Clinical Research career I have handled all phases and functional areas of clinical trials from feasibility through to close-out in a variety of therapeutic areas. I have managed Regional (APAC/AMEA) and Global Clinical Trials at CRO and Sponsor side, respectively, along with line management and Portfolio Management/Program Management responsibilities. In my current role, I serve as the Global Lead Clinical Project Manager for a 400 patient/100 site radiopharmaceutical trial in metastatic Castration Resistant Prostate Cancer (mCRPC). My Clinical Research expertise is further supported by my medical writing and regulatory submission and dossier experience, including with the FDA, EMA, TGA, Medsafe; SOP development and implementation of new systems, including CTMS/eTMF. In my spare time I enjoy keeping up to date with the latest developments in Medical Science and Clinical Research via my podcast and YouTube Channel "Good Clinical".

Charles Beasley speaks the following languages:
No languages available.

Charles Beasley has prior experience in the following industries:
Telix Pharmaceuticals , Telix Pharmaceuticals , Iqvia , Novotech , Novotech , Novotech , Pharmaceutical Solutions Dedicated To Excellence In Clinical Research , Pharmaceutical Solutions Dedicated To Excellence In Clinical Research , Aft Pharmaceuticals , Aft Pharmaceuticals , Lypanosys

Charles Beasley has the following professional experience:
Sapro Consulting And Cro , Telix Pharmaceuticals , Telix Pharmaceuticals , Good Clinical , Iqvia , Novotech , Novotech , Novotech , Pharmaceutical Solutions Dedicated To Excellence In Clinical Research , Pharmaceutical Solutions Dedicated To Excellence In Clinical Research , Aft Pharmaceuticals , Aft Pharmaceuticals , Lypanosys .