Featured Editorial
Focus On Change Management To Aid Technology Adoption
By Ed Miseta, Chief Editor, Clinical Leader

Your employees will always resist technology change. Change tends to bring fear and uncertainty. To overcome fear and make your installation a success, focus on implementation, change management, and providing immediate benefits to users.

Automated Site Payments: Key To Successful Engagement
By Jae Chung, President and Founder, goBalto

The data gathered at investigative sites during clinical trials is the backbone of the pharmaceutical and medical device development process. Without it, assessing the efficacy and safety of therapies would simply be impossible. Whether they are linked to a medical practice, part of an academic medical center (AMC), or operate independently, investigative sites are an important resource.

Industry Insights
A New Paradigm For RTSM Customer Support
Article | By Teresa Goodnough, 4G Clinical

We’ve all had experience calling customer support, whether it’s for your cable, cell service, or health insurance. How many times have you punched zero trying to bypass the automated scripts just to get to a real, live human being? You finally hear a voice (hallelujah!) and you realize very quickly that person cannot answer your question and transfers you to another line (or worse, gives you another number to call).

The Role Of Observational Research And Patient Registries In Evidence Generation
White Paper | By Michael F. Murphy, M.D. Ph.D., Lorna M. Graham, MSc, and Alexandria Malouvier, Ph.D., Worldwide Clinical Trials

Increasingly central in the course of drug development is the inclusion of observational studies, including registries, which provide insights missing from traditional interventional studies.

eTMF + IRB Integration = Efficiency
White Paper | By Michael Smyth, TransPerfect Life Sciences Solutions, and Betsy Fallen, BAFallen Consulting LLC for TransPerfect Life Sciences

The integration of the TransPerfect Life Sciences electronic Trial Master File (eTMF), Trial Interactive, with an Institutional Review Board (IRB) system offers the opportunity for automated oversight, resource optimization, compliance, and an improved patient experience. It also serves as a proof-of-concept to explore opportunities for more integrations.

Adaptive Trial Design In Clinical Trials, Part 2
Guest Column | By Greg Wei, SynteractHCR

Adaptive design is a process that can reduce time and cost without compromising the validity and integrity of the trial. This decision-oriented approach enables the development of personalized medications that provide the best drug to the most appropriate patient, in the right dose and at the right time.

Harness The Power Of The Cloud For Clinical Research Studies
Guest Blog | MedNet Solutions

Take advantage of advanced security and compliance services to ensure that users are safe operating in a cloud environment and that they benefit from the scalability and business continuity of cloud computing.

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