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Clinical Research Associate - Mid West, Hematology, Phase I (Home Based)
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Calling ALL Experienced Clinical Research Associates – Read On, Join the Movement.  


PRA Health Sciences is seeking the best and brightest, nothing less will do.


Who we are: We are 15,000 employees operating in 85 countries committed to saving lives, operating in unison. We are the best at what we do and always strive to be better. We are subject matter and therapeutic experts and each realize that every big change in history has begun with a single step.  The impact is real and significant, we see it every day.  We are making a difference and bringing lifesaving drugs to market faster than ever before and getting them into the hands of the men, women and children who need them.  When there is a team of 15,000 moving forward together with a common goal, given the support, tools and technology needed, that single step becomes a movement. Interested? Come join the movement and discover YOUR PRA.


What’s in it for you?

Ask our CRAs, they will tell you the following… And it’s all true.

  • We promote from within – We provide a career not a job.
  • Culture – There is nothing like it. The proof is in the pudding with 6.5 former PRA employees returning every single month.
  • Tools and Technology – Leading the industry with time saving, intuitive smart technology to help predict trends, anticipate needs and eliminate the need for multiple data entry
  • Security – We are growing and we are dedicated to having you grow with us
  • Mentorship and Training – Our structure provides support for your growth and development as well as questions that arise while on a study at all times
  • Work Life Balance – Its real, we value it. Our strategic solutions and full service models offer you choices for finding a career that includes time for your personal life
  • We are committed to providing our employees with a competitive salary and benefits package with yearly merit and performance reviews


The Clinical Research Associate completes project activities associated with monitoring functions of Phase I-IV clinical research studies.  Perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).


What do you need to have? 

  • Therapeutic Areas: Must have experience monitoring Immuno-Oncology/Hematology trials 
  • Phase I experience preferred 
  • Read, write and speak fluent English; fluent in host country language required
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Minimum of 1 to 2 years of clinical monitoring experience required
  • 4+ years of clinical monitoring experience preferred 
  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience preferred 
  • 4 year degree preferred 
  • Clinical research experience
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Experience in monitoring complex trials

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.


To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.


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