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Senior Clinical Trial Manager - Hematology, Phase I (Home Based)
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Do you want to watch clinical development change, or do you want to be the one to shape it?


Because we’re hoping you’re here for the latter.


Who are we?

We Are PRA.


We are 15,000 employees strong, operating in more than 85 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.


Who Are You?

You are a natural leader with a passion for clinical development. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.


Still here? Good. Because if this is you, we’d really like to meet you.


What will you be doing?

Long story short, you oversee the whole project. As a Clinical Project Manager, you will over see studies for North America and will be the primary liaison to your clients, ensuring questions are answered and issues are resolved. You work together with other project leaders and vendors to keep your project running on time and on budget. You will manage all project deliverables as well your project costs. You will provide feedback to your team throughout its entirety to help improve overall performance. 


What do you need to have?

  • Therapeutic Area: Experience managing Immuno-Oncology/Hematology trials required
  • Phase I experience preferred 
  • At least 3 years of demonstrated experience delivering process and system improvement in one or more of the following disciplines and/or functional areas
  • Minimum 5 years experience in clinical research, including a minimum 2 years full service project management experience or an equivalent combination of education and experience sufficient to successfully perform the key responsibilities of the job.
  • Drug Development, Early Development thru Post‐Marketing (phases I‐IV); Clinical trial/project development, Data management, Project management, Safety Pharmacovigilance, Financial management tools, Resource management, Regulatory compliance (ICH‐GCP), Quality Management (ISO, Six Sigma, etc.), Technology management
  • Read, write and speak fluent English; fluent in host country language required.
  • An undergraduate degree in life sciences, business, or information technology from an accredited institution or international equivalent degree
  • 4 year degree preferred
  • Project management certification (PMI, PMP) preferred 

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.

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




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