Meet the PharPoint Team: Carson M., Biostatistics Manager

PharPoint Biostatistics Manager, Carson M. is a team player and loves the group mentality to get the job done correctly and on time. 

“Everyone’s trying to get to the same place, Carson says.  That sense of teamwork is continued in his personal life, as he and his wife are expecting twins this April. “I’m excited to grow the family and see how my wife and I manage that.”  

 RELATED RESOURCE Exploring Standard Biometrics CRO Timelines  

Carson describes himself as understanding and passionate, two qualities very apparent in his role as Biostatistics Manager.  

“I’m responsible for two direct reports currently, helping out the newer staff and doing my best to keep things moving day to day, he explains. His day-to-day consists of meeting with clients, where he sets and manages deliverable timelines and expectations, and communicating with his team to coordinate a successful product.  

 When asked what his biggest lesson learned while working in the healthcare field was, Carson highlighted the importance of working well together. 

“There’s always someone on the other side, you know?” Carson explains. Everyone’s trying to do their best. Just having patience and working with people in a more collaborative fashion will get you a lot further than trying to do it yourself.”  

This collaborative mentality is one of Carson’s favorite things about working at PharPoint Research.  

“I just find everybody’s personalities to blend well with mine,” he says. Everyone’s very willing to help each other and just kind of take time to talk, if you want to. We stay busy, but I think we have a good group of people.” 

When not managing a team at PharPoint, Carson describes himself as a “nerd for history and science,” and enjoys reading and listening to podcasts about those subjects. Lately, he’s found himself gravitating towards shipwrecks. Those podcasts are usually listened to while hiking and spending time in nature – I think it’s really cool to just kind of explore the world around us.”  

Carson’s journey to PharPoint started at Western Michigan University, where he obtained his bachelor’s in math and became a Teacher’s Assistant to cover his way through a two-year master’s program. 

Upon graduating, he started working at a CRO as a statistical programmer. The COVID-19 pandemic later pushed him to explore other opportunitiesI started looking to try and get more into a biostatistics roleand just wanted to see what else was out there. I had an interview at PharPoint and kind of never looked back.” 

 

While PharPoint offers services in numerous therapeutic fields, Carson often finds himself in the Oncology space 

“I think oncology is interesting, because it kind of gets a bad rep. It’s a challenging therapeutic area for all kinds of reasons, but I think when you have success in the oncology field, it’s a pretty cool feeling. It’s just such a big thing that impacts so many people, so to be able to help out with it…it’s pretty exciting.”


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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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