Clinical Trial Gurus

OCTOBER 17, 2021

Clinical research coordinator is the most important role in any clinical trial. In this video we discuss the top mistakes that all coordinators make and how to potentially avoid these issues.

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Clinical Trial Gurus

JUNE 30, 2021

One of the more important teaching points in our CRC Academy is adverse event reporting for clinical research coordinators. In this video I share some tips for clinical trial coordinators who are tasked with proper reporting documentation and processing.

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Clinical Trial Gurus

MAY 3, 2021

A Clinical Research Coordinator talks about some of the barriers that he has encountered while working on remote clinical trials.

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Clinical Research Coordinator Clinical Research Clinical Trials Clinical Trials 52

Clinical Trial Gurus

MAY 24, 2021

Depending on the research site, Clinical Research Coordinators (CRCs) are responsible for several clinical trial activities ranging from regulatory document management to patient intake or budget negotiations.

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Clinical Trial Gurus

AUGUST 18, 2021

Oncology clinical research is a world of its own. In this video I speak with a clinical research coordinator who shares her own experiences in the world of oncology clinical trials. Full of challenges, different medical terminology, graded adverse events and so much more.

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Clinical Research Coordinator Clinical Research Clinical Trials Clinical Trials 52

Clinical Trial Gurus

JULY 7, 2021

Creating source document templates for a clinical trial is a task that more often than not falls into the responsibility parameters of a clinical research coordinator. In this interview, I discuss this lesser understood study coordinator function with a clinical research site director.

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XTalks

FEBRUARY 13, 2023

Guarnaschelli reviewed the medical considerations involved in radiopharmaceutical clinical trials. Watch the free, on-demand webinar to gain valuable insights from a group of experts about implementing radiation dose limits in radiopharmaceutical clinical trials. How does Radiation Cause Cell Death?

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Clinical Trial Gurus

JULY 5, 2021

Clinical research professionals can come from many different career backgrounds. In this example, one of my current clinical research coordinators shares her story of starting out as a medical biller at a medical clinic that also happened to conduct a few clinical trials.

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XTalks

FEBRUARY 22, 2021

Clinical research is part of a growing industry that provides individuals with rewarding career options and a ladder to climb. Working in the clinical trials industry allows clinical researchers to work with patients and bring new drugs to market. Clinical Research Coordinator.

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Clinical Trial Gurus

AUGUST 24, 2021

Adverse events are a part of every clinical trial, if not a part of every study subject’s journey throughout a study. An important facet of a clinical research coordinator’s job responsibilities are effectively identifying, reporting, and documenting adverse events.

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Clinical Research Coordinator Clinical Research Clinical Trials Clinical Trials 52

Clinical Trial Gurus

AUGUST 21, 2021

A clinical research coordinator compares industry sponsored trials and investigator initiated trials in terms of working on the studies from a CRC perspective.

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ACRP blog

SEPTEMBER 28, 2022

It wasn’t just the resignation of yet another clinical research coordinator (CRC) that Christina Brennan, MD, CCRC, vice president for clinical research at Northwell Health, had to contend with earlier this year. Welcome to the war for clinical trial talent, 2022 style. We have approximately 2.5

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ACRP blog

JANUARY 12, 2023

. “We are focusing on schools in minority communities near oncology clinical trial sites,” explains Clark. Under-representation of racial and ethnic groups in the clinical research workforce contributes to the under-representation of diverse clinical trial participants, most notably in oncology clinical trials.

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ACRP blog

OCTOBER 11, 2022

For Christina Brennan, MD, CCRC, vice president for clinical research at Northwell Health, it’s time for industry to rethink how it recruits and retains talent. Brennan is a big advocate of giving clinical trial team members clear career paths and opportunities for professional development.

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ACRP blog

FEBRUARY 2, 2023

“We often hear that clinical research professionals ‘accidentally happened upon’ this career path,” adds Lisa Lionetti-Freutel, CCRC, Clinical Research Coordinator at Renown Health.

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ACRP blog

DECEMBER 14, 2022

Taking the guesswork out of assigning trials. Assessing the capacity of a clinical research coordinator (CRC) is one of many challenges involved in managing clinical trials—which are heterogeneous and increasingly complex, with rising regulatory burdens and tight budgets. View complete schedule. .

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Clinical Trial Gurus

AUGUST 22, 2021

Regulatory documents are essential for every clinical trial. As a clinical research coordinator or clinical research associate it can be helpful to know which documents typically cause cascades for other documents.

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Clinical Trial Podcast

JANUARY 23, 2022

One of the most time and resource intensive tasks in clinical research is data entry. . Clinical research coordinators spend countless hours transferring clinical data from a patient’s Electronic Health Record (EHR) into a study specific Electronic Data Capture (EDC) system. Hugh holds a Ph.D.

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ACRP blog

DECEMBER 28, 2022

From AI and machine learning producing an era of rapid new pathways, to an industry-wide push for equitable representation in clinical trials, 2023 will be a catalytic year for biopharma clinical development and commercialization,” the company notes in its press release on this, its 13th annual trends report.

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ACRP blog

MAY 22, 2023

This builds background knowledge with an ACRP training course titled ‘CRA Core Competency Foundations’ and carousel training, which involves four training sessions focusing on the various phases of clinical trials and Merck’s global processes for those phases.

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ACRP blog

JANUARY 10, 2023

Remote working during the pandemic raised new challenges in resolving conflict between the various stakeholders in the clinical trials ecosystem. A clinical research coordinator (CRC) interacts with a clinical research associate (CRA) who isn’t prepared for monitoring visits and doesn’t make the CRC aware of timelines ahead of time.

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ACRP blog

JANUARY 31, 2023

To that end, I became certified as a clinical research coordinator (CCRC) by ACRP in 2010 and then as a principal investigator (CPI) in 2015 after I earned my doctorate. My goal is for everyone in the clinical research industry to recognize ACRP certification as the certification to get.

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ACRP blog

NOVEMBER 30, 2022

There is a growing expectation that clinical trial sites should be tech-enabled, based on experiences during the COVID-19 pandemic and even earlier. There are often multiple platforms, which can differ by sponsor, leaving our clinical research coordinators (CRCs) drowning in passwords for access to the various portals.”.

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VirTrial

MARCH 11, 2020

Coronavirus and Ongoing Clinical Trials. Fear of traveling to a hospital or clinic may be enough to negatively impact enrollment and recruitment of ongoing trials. Coronavirus and Trials in Startup. In light of travel restrictions regarding the Coronavirus, timelines of new trials in startup are in danger of delay.

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VirTrial

SEPTEMBER 21, 2020

By eliminating the need for Clinical Research Associates (CRAs) to travel, Virtual Pre-Site greatly reduces time requirements, slashes associated costs for clinical trials, and enables existing studies to continue and new studies to start amidst the monumental COVID-19 challenges. .

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VirTrial

MAY 26, 2020

Scottsdale, AZ (May 26, 2020) – VirTrial today announced a new service designed to enable virtual site monitoring visits in the clinical trials industry. The solution enables pharmaceutical sponsors and CROs to evaluate, qualify and routinely monitor research sites for studies without physical travel.

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XTalks

MAY 14, 2021

Here are three ways to advance your career in clinical research. To learn more about what it takes to progress from a CRA to a project manager or clinical trial manager position in less than two years, register for this free webinar hosted by trial experts from ICON’s functional service provision (FSP) division, DOCS.

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