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“By using DrugDev’s Site Activation team and technology we cut the contracting cycle time by 42% over the prior year. DrugDev’s expertise, personalized service and technology made my life easier. ” 

CLINICAL MONITORING MANAGER, 
ACTELION
Melissa Easy

ASK AN EXPERT: SITE ACTIVATION

DrugDev welcomes you to a new series of quick and relevant deep dive Q&A with subject matter experts discussing important topics in clinical research. 

Over the coming weeks and months, we'll feature one question, with one answer, on a variety of topics. Each video is approximately one minute long and addresses detailed questions.

We'll be adding new videos all the time, so be sure to check back often for more expert Q&A!

Meet Our Experts

Melissa Easy
Founder and Global Head of Strategic Accounts

Activate Your Sites 25% Faster

Schedule a demo of DrugDev Spark to learn how you can activate your sites faster and more efficiently.

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2. What kind of time savings are realistic from tech?

3. What are some tips for expediting the contracting process?

4. When do you recommend working on IRB and regulatory docs?

5. Can we ever remove people and rely on tech only?

ASK AN EXPERT: 

SITE ACTIVATION

2. What kind of time savings are realistic from tech?

3. Tips for expediting the contracting process...

4. When do you recommend working on IRB and regulatory docs?

5. Can we ever remove people and rely on tech only?

1. Why is tech important in site startup?

1. Why is tech important in site startup?

Melissa Easy

Jim DiCesare
VP and General Manager, Site Startup

Melissa Easy

JoAnn Ulmer
Contracts Manager

Rebecca Arch
Senior Contracts Manager

Melissa Easy
Melissa Easy

Sharon Gordon
VP, Contracts

1:31 |  Melissa Easy, Founder and Global Head of Strategic Accounts

1:07 |  Jim DiCesare, VP and General Manager, Site Startup

1:35 |  JoAnn Ulmer, Contracts Manager

1:53 |  Rebecca Arch, Senior Contracts Manager

1:18 |  Sharon Gordon, VP, Contracts 

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