June, 2019

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10 Interview Questions Clinical Research Managers Will Ask You

ECRG Media's Clinical Research Podcast

10 Interview Questions Clinical Research Managers Will Ask You In this episode I detail 10 interview questions clinical research hiring managers will ask you during the interview process. I hope you enjoy! Don't forget to Subscribe for new content! Subscribe: [link] Call or Text: 910-502-3732 Email: eliteclinicalgroup@gmail.com Podcast: [link] Steemit: [link] Advertise: eliteclinicalgroup@gmail.com Watch: » Industry News: [link] » All Videos: [link] » Interview Recaps: [link] » Glassdoor Reviews

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Orphan medicines launch excellence: sustaining launch success

pharmaphorum

Launching orphan medicines excellently will become even more important over the next five years as more patients with rare diseases have pharmacotherapies available. There are also a growing number of disease-focussed registries, increasing public and policy maker awareness, and significant R&D investment in orphan drugs, as well as in digital technologies to support trials and treatment.

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Talent Acquisition Techniques of Top Healthcare Providers

Pharma Focus Asia

Recruitment within the healthcare industry is becoming especially tough as shortages and gaps within specialities are more prevalent. It has been estimated that there will be a shortage of approximately 45,000 medical and surgical specialists within the next ten years. Further, the medical industry is also experiencing a shortage of non-clinical staff, like security guards, […].

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Which One Is Better – Pharma Marketing Company Or Pharma Manufacturing Company?

Fossil Remedies

Pharma Marketing Vs Pharma Manufacturing. Every year thousands of students pass the degree in pharmaceuticals with a lot of aspirations and dreams. Not everyone of them achieves the desired place; not because the sector doesn’t have enough opportunities or scope, but they fail to choose the right path. Whether to join a pharma marketing company and start marketing the products or open a manufacturing company; the decision is crucial.

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Unlocking Excellence: How Catalent Is Transforming Japan’s Clinical Research

Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud

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How TrialKit Can Aid in Virtual Clinical Trials

Crucial Data Soutions

Although approach differs slightly amongst organizations in clinical research, everyone agrees on this: it’s time for the industry to become more agile. Too many life-saving treatments and medical advancements are at stake to remain attached to the traditional ways of data collection. Over the past ten years, we’ve seen things slowly going the way of virtual clinical trials.

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Pharma Packaging Solutions Expanding Capacity and Services

Pharma Packaging Solutions

With two busy 2019 quarters booked, Pharma Packaging Solutions knew it needed to expand capacity quickly. Investments totaling over $2,7 million were made in several areas. One major investment included additional portable serialization and aggregation equipment to improve efficiency on primary and secondary lines. Additional labeling equipment was ordered and installed along with a leading-edge environmental control system.

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Amazon’s Pharmacy Should Support Importation to Offer Lower Drug Prices

Pharmacy Checkers

Originally published on LinkedIn. With drug prices in the spotlight of our national healthcare debate, one could certainly view Amazon’s entry last year into the pharmacy space as a welcome development. After all, when it comes to upending traditional business models by undercutting their prices, Amazon is king. For Americans, the tens of millions who don’t fill prescriptions each year because of cost, relief can’t come soon enough.

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United Therapeutics - Glassdoor Review - EP. 8

ECRG Media's Clinical Research Podcast

In this episode we talk about United Therapeutics. The first sponsor in the glassdoor review series. I hope you enjoy this one. Don't forget to Subscribe for new content! Subscribe: [link] Call or Text: 910-502-3732 Email: eliteclinicalgroup@gmail.com Podcast: [link] Steemit: [link] Advertise: eliteclinicalgroup@gmail.com Watch: » Industry News: [link] » All Videos: [link] » Interview Recaps: [link] » Glassdoor Reviews: [link] We do: » Insider Interviews » Resume Reviews » Question and Answer »

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United Therapeutics - Glassdoor Review - EP. 8

ECRG Media's Clinical Research Podcast

In this episode we talk about United Therapeutics. The first sponsor in the glassdoor review series. I hope you enjoy this one. Don't forget to Subscribe for new content! Subscribe: [link]. Call or Text: 910-502-3732. Email: eliteclinicalgroup@gmail.com. Podcast: [link]. Steemit: [link]. Advertise: eliteclinicalgroup@gmail.com. Watch: » Industry News: [link]. » All Videos: [link]. » Interview Recaps: [link]. » Glassdoor Reviews: [link].

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Most Frustrating Thing About Dealing With Sites

ECRG Media's Clinical Research Podcast

Most Frustrating Thing About Dealing With Sites In this episode I discuss some of the most frustrating things I have dealt with when dealing with sites. From the perspective of an InhouseCRA/ Clinical Research Associate I detail the most frustrating things about dealing with Clinical research sites. Don't forget to Subscribe for new content! Subscribe: [link] Call or Text: 910-502-3732 Email: eliteclinicalgroup@gmail.com Podcast: [link] Steemit: [link] Advertise: eliteclinicalgroup@gmail.com Wat

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The New Age of Decentralized Clinical Trials

White paper that delves into the complex topic of Decentralized Clinical Trials and how to master them within the confines of FDA Regulations

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Most Frustrating Thing About Dealing With Sites

ECRG Media's Clinical Research Podcast

Most Frustrating Thing About Dealing With Sites. In this episode I discuss some of the most frustrating things I have dealt with when dealing with sites. From the perspective of an InhouseCRA/ Clinical Research Associate I detail the most frustrating things about dealing with Clinical research sites. Don't forget to Subscribe for new content! Subscribe: [link].

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How Much PTO Should I Hold Onto?

ECRG Media's Clinical Research Podcast

How Much PTO Should I Hold Onto? For those brand new to the working world, taking PTO is something you will have to get used to. How much PTO should I use, how much should i save for a rainy day? In this episode we break it down. Don't forget to Subscribe for new content! Subscribe: [link] Call or Text: 910-502-3732 Email: eliteclinicalgroup@gmail.com Podcast: [link] Steemit: [link] Advertise: eliteclinicalgroup@gmail.com Watch: » Industry News: [link] » All Videos: [link] » Interview Recaps: [l

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How Much PTO Should I Hold Onto?

ECRG Media's Clinical Research Podcast

How Much PTO Should I Hold Onto? For those brand new to the working world, taking PTO is something you will have to get used to. How much PTO should I use, how much should i save for a rainy day? In this episode we break it down. Don't forget to Subscribe for new content! Subscribe: [link]. Call or Text: 910-502-3732. Email: eliteclinicalgroup@gmail.com.

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Non-Partisan Support of Prescription Drug Importation State Laws Deviate from the National Political Norm

Pharmacy Checkers

Trump supports prescription drug importation, and he’s not alone. An article by Kaiser Health News reporter Phil Galewitz headlined Trump’s support for drug importation to fight high drug prices at the state level. His article delves into the history of earlier state importation attempts, which were personal drug importation not wholesale drug importation programs.

Drugs 60
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How Machine Learning Drives Clinical Trial Efficiency

Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.