Transitioning from the lab to a Clinical Research Associate job

New Scientist recently published a career ‘case study‘, detailing how Linda Murray, a parasitologist and research assistant made the transition from the lab to a coveted job as a clinical research associate. After sending some resumes, she was lucky to land a role as a clinical trial associate with a CRO — an entry level step that gave her a good overview of the clinical research process.

Unfortunately, the article is not tremendously enlightening about what aspect of Linda’s approach led to her success. She had a friend who was already working as a CRA, which may have helped her to network and put her resume in front of the right people. Additionally, being able to ask someone who’s knowledgeable for insight into the industry can be a huge advantage — that’s basically what an informational interview is all about. Sometimes, luck plays a role as well — if a CRO has just landed a contract for a big new trial, they may need to quickly adjust their staff levels to manage the workload. You may be able to give yourself  an edge and increase your chances of being in the “right place at the right time” by reading trade magazines and industry newswatch websites to find out when trials are announced or contracts are awarded.

We’ve published a number of articles about the CRA career path that may help you find your own way to a career in clinical research.  Please check them out — and good luck in your search.

 


Posted: July 26th, 2011 | Author: | Filed under: Clinical Research Associates | Tags: , , , | No Comments »

What’s it like to work for a CRO?

Over at ask.metafilter, someone has posed the question “what’s it like to work for a CRO?”

The person asking the question is a university research assistant with a background in cognitive neuroscience and an interest in statistics and applied math.

So far, one excellent answer has been posted. Read the rest of this entry »


Posted: June 12th, 2011 | Author: | Filed under: Clinical research, Preclinical R&D | Tags: , , , , | No Comments »

The future of CRA jobs

Clinical Research Associate jobs are in high demand. CRA jobs pay well, are often home-based, and offer a relatively high degree of personal autonomy. It’s a job that offers a good mix of solo time as well as working with others, and it’s a job where you can really feel like your work matters, because you’re contributing to the safe development of new drugs that can improve lives. The CRA role hasn’t changed a great deal over the years, with the exception of the increasing adoption of electronic methods for collecting case reports. But the nature of CRA employment has changed and is continuing to shift as companies change the way they do business. This article will discuss the four most common CRA employment arrangements and make some predictions for the future. Read the rest of this entry »


Posted: February 11th, 2009 | Author: | Filed under: Clinical research, Clinical Research Associates | Tags: , , , , , , , , | 8 Comments »

How to write a clinical research associate resume

This post will help you write a resume for clinical research jobs: entry-level clinical research associate jobs, clinical research coordinator jobs or clinical trial associate jobs would be good targets for this advice.

The hardest step to a successful career in clinical research is the first one. Getting your foot in the door takes patience, preparation, ingenuity and a toolkit of supporting materials and behaviors that will make you stand out above the competition.  A well-crafted resume can help you get your chance to shine as a clinical research associate, medical science liaison or other pharmaceutical professional.

There are a million guides out there that will give you good general advice on writing and formatting your resume, and (with one important exception) I’m not going to waste your time by duplicating that advice here. These tips are specific to the clinical research field. If you’re applying for entry-level clinical research associate jobs, the following suggestions may help your resume get noticed. Read the rest of this entry »


Posted: January 29th, 2009 | Author: | Filed under: Clinical research, Clinical Research Associates, ICH-GCP, Resumes & CVs | Tags: , , , , , | 13 Comments »

CRA training: How NOT to conduct a site visit

Here’s an amusing look at a day in the life of a CRA (Clinical Research Associate) on a site visit. This video is a parody, but it does give you a sense of what site visits are all about.

A CRA may spend 60-80% of their time on the road conducting these visits.  Their job is to monitor the conduct of clinical trials, ensuring that research sites are enrolling patients and carrying out the trial correctly, following both the trial protocol and ICH-GCP conduct guidelines. They review a lot of documentation, check site supplies and generally watch out for problems.

When there are problems, a CRA needs to help get the clinical site staff back on the right track, and so they need to have excellent communication and negotiation skills.  It can take a lot of diplomacy to get clinical investigators and their staff to change the way they do things in a busy clinic!

The sound in the embedded clip isn’t synchronized quite right.  You can see a higher-quality version at the ResearchPoint site.  They are the CRO (Contract Research Organization) that created the video.

You can read more about what a CRA job is all about in this earlier article.


Posted: January 27th, 2009 | Author: | Filed under: Clinical research, Clinical Research Associates, Fun | Tags: , , , , | No Comments »