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September 9, 2020
Interning at PharPoint_Statistical Programming

Interning at PharPoint Research

Dedicated to developing careers in the CRO industry

Just as we’ve been passionate about helping clients improve global health, PharPoint has been adamant about offering students who are just as passionate about improving global health as we are the mentorship they need to thrive in the clinical research industry.

PharPoint offers internships across a range of functions, including statistical programming, clinical operations, data management and administrative/operational internships.

Three of PharPoitn’s statistical programming interns, all pursuing degrees in higher education, share their experience at PharPoint:


CAREERS Join PharPoint as we help innovative sponsors shape a healthier tomorrow.  

 

PharPoint’s company culture

While the culture shifts that come with working from home can be challenging at first, PharPoint has worked to ensure that internship participants are supported.

Our 2020 summer participants spoke highly of the support they have received from their fellow employees at PharPoint, and how invested employees were in the future of the industry.

“My boss has truly been the best I’ve ever had,” says 2020 statistical programming intern Kayla. In her intern experience at PharPoint, she’s found that the support her manager provides her has truly allowed her to take on new skillsets and continue her career growth.


RELATED ARTICLE Ensuring High Quality Statistical Output  

“My boss has truly been the best I’ve ever had.”

Fellow statistical programming intern Michael agreed. “Employees at PharPoint are so helpful, and are able to provide direction when needed.”

While working from home has brought its challenges, it’s also brought new skills to the internship experience.

Participants reported improvement in their programming skills and strengthening their ability to work independently while also collaborating with various departments.

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EBOOK

Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs

This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).

Exploring Standard CRO Timeline Benchmarks

Preparing to work with a top biometrics contract research organization and wondering how their promised data management, biostatistics, and medical writing timelines match up to the industry average? To help sponsors dig into these details and ensure the timelines they’re receiving are competitive, we’re providing PharPoint’s typical timelines alongside research that calculates industry standard timelines, when available.

Our hope is that this document can help sponsors set realistic expectations, confidently ask the right questions of their vendors, and ultimately, partner with a top biometrics CRO that keeps their study moving: because patients are waiting.

 

eBook contents include:

PharPoint’s short eBook, Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs, includes the below information.

  • Standard database build timeline
    • The bigger picture: Considering site identification and study start-up
  • Standard mid-study database change timeline
  • Standard database lock time
    • Six strategies for a faster database lock
  • Evaluating database lock to top line results timeline
    • Ensuring a rapid delivery
  • Evaluating database lock to delivery of tables, listings, and figures (TLF) timeline
  • Standard clinical study report delivery timeline
  • About PharPoint Research

Compare Standard Clinical Trial Timelines

For instant access to the eBook, fill out the form below.

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Interning at PharPoint Research | Clinical Operations, Marketing, Administration
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