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Param Singh

Param Singh has been working in the life sciences industry his entire career. As the director of clinical trial management solutions at Perficient, he developed the clinical trial management team to become one of the best in the industry. Param leads a highly skilled team of implementation specialists and continues to build lasting relationships with clients. He has a knack for resource and project management, which allows clients to achieve success. Param has been with Perficient, via the acquisition of BioPharm Systems, since 2008. Prior to joining the company, he guided the clinical trial management group at Accenture.

Posts by this author:

Life Sciences Site Monitoring with Robotic Process Automation

Previously, I discussed fixing clinical trial challenges with robotic process automation. This blog analyses site monitoring, and how robotic process automation (RPA) can enhance it. While sponsors, CROs, and sites all acknowledge that site monitoring is a necessary part of ensuring clinical trials are run in compliance with governing regulations and protocols, it can be […]

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Register for This Webinar to Learn More About Siebel CTMS IP2019

Has your organization been thinking about upgrading your Siebel Clinical Trial Management (CTMS) system to the latest version available, but aren’t exactly sure what the potential benefits an upgrade could bring? With the newest version of Siebel, Innovation Pack 2019 (IP2019), there are some significant updates that bring key features and benefits to end users. […]

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Life Sciences Companies Can Establish Better Relationships

It used to be that a doctor was a patient’s only touch point for a diagnosis and prescription. Today, patients have many more avenues to get the information they seek, which has led to higher expectations from patients. Fortunately, life sciences companies have the opportunity to understand, educate, and treat patients by successfully engaging them. […]

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Addressing Clinical Trial Challenges with Robotic Automation

The success of any given clinical trial depends heavily on the relationship between the sponsors and study sites. This is more important than ever since life sciences and healthcare companies are undergoing a digital transformation. The evolving trend towards patient-centric trials, combined with the introduction of digital technology solutions that improve clinical trials outcomes, means […]

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iHelp Lifecycle and Version Control in Life sciences

Previously, I examined how to develop content and implement iHelp. In this final installment I discuss the iHelp lifecycle and control. iHelp comes with a built-in version control system. When you create a new iHelp article, it starts at version 0, with a status of “In Progress.” You then enter and edit the content, testing […]

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Administering iHelp and Developing Content in Life Sciences

My previous blog highlighted the useful cases of iHelp. This blog will examine how to develop content and implement iHelp. iHelp is developed and administered through the Administration iHelp screen. The Designer view provides a Java-based workflow editor, which is very much like a simple version of Microsoft Visio. You drag the steps onto the […]

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When is Oracle’s iHelp Useful?

Previously, I outlined how iHelp can assist administration. This blog will highlight the useful cases of Oracle’s iHelp. iHelp is useful for tasks of different complexity. You can use iHelp for short data entry-type tasks, like entering a new subject for a site in which you list out the steps and give field descriptions and […]

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Oracle’s iHelp Assists Administration

My last blog looked at the end-user benefits that iHelp provides. This installment explores how Oracle’s iHelp can assist administration. iHelp also has plenty of benefits in terms of administration. One of the great parts about this help system is that no back-end configuration needed – no use of Siebel Tools required. You can make […]

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[Perspective] Why Pfizer Implemented Oracle CTMS in the Cloud

Many companies in the life sciences industry experience rapid global growth, both organically as well as through merger and acquisition. While growth is, of course, great and welcome, it also comes with some challenges. With respect to clinical operations and clinical trial management, aligning processes can be rather challenging as different parts of the business […]

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End-User Benefits of Oracle’s Cloud Siebel CTMS iHelp

Previously, I discussed iHelp and all the assistances it provides. This blog looks at the end-user benefits that Oracle’s Cloud Siebel CTMS iHelp provides. One of iHelp’s key end-user benefits is that the content is available on demand, directly in Siebel – there’s no need to dig through a user manual or even divert your […]

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[Perspective] A Cloud CTMS Was a Requirement for Pfizer

While Pfizer’s IT team had been supporting the legacy CTMS and other clinical systems for many years, the company’s current strategy centers on implementing cloud solutions. The reason for this approach is to reduce the burden on internal resources and reduce the need to invest in IT infrastructure. Having different, nuanced processes and decentralized data […]

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What is Oracle’s Siebel CTMS iHelp Program?

Previously, I introduced iHelp and how this program can help you work Oracle’s Cloud Siebel CTMS. This blog will analyze with iHelp truly is. iHelp is a context-sensitive, interactive, and highly customizable on-screen help tool. It keeps track of where you are in the system and adjusts content accordingly. It is interactive in that it […]

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Real-Time Assistance in Oracle’s Cloud Siebel CTMS with iHelp

Have you ever found yourself stuck on a task in Oracle’s Siebel Clinical Management System (CTMS), or even forgotten how to perform a task altogether? While you may have a comprehensive user guide, it’s probably quite lengthy and cumbersome. Wouldn’t it be nice if Siebel CTMS had a guide built right into the application that […]

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Reimagining the Way Life Sciences Companies Do Business

Digital transformation is a term that is being thrown around quite a bit in every industry and sector. But it is frequently misunderstood or misrepresented. Companies are trying to stay relevant and current by adopting specific new technologies to claim their move towards digital transformation. But it is much more than simply using new technology. […]

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How Can AI Be Used For Clinical Trials?

The continuous innovation of technology is changing the way companies operate across different sectors. In particular, big data and artificial intelligence (AI) are expected to have the most significant impact. In this post, we’ll discuss how big data and AI can be used to support clinical trials in a variety of ways. How does big […]

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Implementation of Siebel CTMS in the Oracle Cloud: Session Recap

Yesterday, I was fortunate to have been able to present with Pfizer at Oracle Health Sciences Connect 2019 on Perficient’s implementation of Oracle’s Siebel Clinical Trial Management Systems (CTMS) in the Oracle Cloud for the company. On stage at @OracleHealthSci Connect with @pfizer, discussing our implementation of #Siebel CTMS in the #Oracle #Cloud for the […]

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Key Takeaways About Compliant IT Systems In The Cloud

This is the final post in our series on maintaining regulatory-compliant IT systems in the cloud. In this post, we’ll go over the key takeaways from the series and then we’ll send you on your way! Regardless of how much control you have over your IT systems, if you are using them for regulatory purposes, […]

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Tips And Best Practices For Compliance In The Cloud

As we’ve learned in the previous posts in this series, having a thoughtful, thorough cloud vendor qualification process and intelligent SLAs in your cloud vendor contracts will help you maximize the value of the cloud while maintaining regulatory compliance. In addition, here are some tips and best practices to help you knock it out of […]

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How To Use Contracts For Regulatory Compliance Of Cloud Systems

In my previous post in this series, we discussed how to qualify cloud vendors. Once that process is complete, the second step to maintaining compliance is to document your specific regulatory requirements in a contract with the cloud vendor, usually in the form of service-level agreements (SLAs). In this blog post, I include a range […]

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How To Qualify Cloud Vendors

We recently completed a 21 CFR Part 11 gap analysis engagement for a client that was largely using SaaS applications, but had no cloud vendor qualification process in place. They had just been allowing each business unit to select the applications that met its user requirements, accept whatever validation documentation the cloud vendor supplied (if […]

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