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Welcome to Clynergy.

/ˈclinərjē/


Noun.
The reciprocal action of two or more groups, sources, or other factors to produce an effect that is greater than the effects of each separate source in furthering clinical advancements for the benefit of humanity.

The Clynergy Difference

When you want real results on your next trial, look no further. Our process is second to none. Clynergy brings over 15 years of  clinical research experience in both North America and Europe, and we specialize in supporting smaller sponsor companies and CROs in the conduct of national and international clinical trials. With our expert support, you will save valuable time and resources managing your studies, as well as navigating unfamiliar regulatory environments.

1

Brief

Class aptent taciti sociosqu ad litora torquent per conubia nostra, per inceptos himenaeos. Nulla nunc dui, tristique in semper vel.
2

Analysis

Class aptent taciti sociosqu ad litora torquent per conubia nostra, per inceptos himenaeos. Nulla nunc dui, tristique in semper vel.
3

Planning

Class aptent taciti sociosqu ad litora torquent per conubia nostra, per inceptos himenaeos. Nulla nunc dui, tristique in semper vel.
4

Execution

Class aptent taciti sociosqu ad litora torquent per conubia nostra, per inceptos himenaeos. Nulla nunc dui, tristique in semper vel.

Services

 

CLINICAL

Our goal is to help you bring your leading-edge products and therapies into a clinical trial setting where patient safety is key and quality results, a must.  Moreover, as you step onto the overseas regulatory terrain, we can help you bridge the cultural, communication, and compliance differences that can – and often do – result in undesirable consequences in the conduct of clinical trials.

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MEDICAL WRITING

When it comes to high-quality medical and technical writing, we usually think in terms of streamlined, polished, and error-free documents. But what about the relevance of the content and its success rate in the clinic? The answer here lies in knowing your audience.  That’s why we build upon our diverse experience to help clients deliver high-caliber products that are also highly relevant and successful.

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QUALITY ASSURANCE

With human lives at stake, quality is more than just an added value in clinical research.  It’s a legal and moral obligation, as well as critical benchmark for tracking both product safety and efficacy within the context of reliable study data, regulatory compliance, and teamwork.  But that can be a tall order when your QA department is thousands of miles away from the study site.  Clynergy bridges that gap to better connect quality assurance to the study.

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TRAINING

Like any other rapidly changing field, clinical research demands continuous access to high quality professional development that is relevant and experiential, customized and cost-effective.  And given our extensive training experience, we can help you stay on top of your training needs – whether onsite, online, or in the field – in such critical areas as patient safety; regulatory compliance; quality data collection; and ethical study management.

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CLINICAL

Our goal is to help you bring your leading-edge products and therapies into a clinical trial setting where patient safety is key and quality results, a must.  Moreover, as you step onto the overseas regulatory terrain, we can help you bridge the cultural, communication, and compliance differences that can – and often do – result in undesirable consequences in the conduct of clinical trials.

LEARN MORE

MEDICAL WRITING

When it comes to high-quality medical and technical writing, we usually think in terms of streamlined, polished, and error-free documents. But what about the relevance of the content and its success rate in the clinic? The answer here lies in knowing your audience.  That’s why we build upon our diverse experience to help clients deliver high-caliber products that are also highly relevant and successful.

LEARN MORE

The Clynergy Team is Led By Ned French

Ned's Bio

Ned French is a well-rounded expert in the field of clinical research, with more than 12 years of experience in a variety of management and administrative capacities, including Project Manager, Training Manager, Lead CRA, Sr. CRA, CRA, and Clinical Project Coordinator. He has overseen sites in Phase I facilities, major university hospitals, smaller hospitals, and private practices throughout North America and Europe, working in a broad range of therapeutic areas, including hematology, immunology and vaccines, neurology, pain management, wound management, infectious diseases, and surgery.

Mr. French specializes in project and site management; contracts and budgets; clinical training and CRA development; auditing; medical and technical writing; vendor and partnership management; translation management; systems implementation; and feasibility assessments. In addition to having managed more than 30 in-house studies in support of placebo and product delivery prototype development, he has actively served on over 40 clinical trials, including orphan, biologic, pharmaceutical, and medical device trials.

Having steadily worked his way up through the ranks, in both sponsor companies and clinical research organizations, Mr. French not only understands the “bigger picture,” he also knows first-hand the power of synergistic teamwork in conducting successful clinical trials. What’s more, he has spent the last several years in the international marketplace. Consequently, he is uniquely positioned to design and deliver consulting services that are project-relevant, highly customized, and culturally sensitive.

Mr. French holds a Bachelor of Science degree in Psychology, as well as two high-profile industry certifications – Certified Clinical Research Associate (CCRA) and Certified Clinical Research Professional (CCRP) – which speak to his proven knowledge of the regulations, guidelines, and best practices in the field of clinical research. He is also fluent in English and German.

Experience Counts

 

Years of Experience

Countries Monitored

In-House Studies

Clinical Trials

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