PRAHS

Returning Candidate?

2017-43388

2017-43388

Title 
Clinical Study Manager- Home Based
Job Locations 
-
Canada-Remote
Posted Date 
10/17/2017

More information about this job

Overview

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 12,000+ employees strong, operating in more than 80 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 life saving drugs into the hands those who need them most.

 

Who are you?

You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. 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.

Responsibilities

What will you be doing?

As a Clinical Research Manager (CRM) you have a  significant  impact  on  how  a  country  can  deliver  country-specific  trial commitments and objectives. As a customer-facing role, this position will build business relationships and represent the client with investigators, functional outsourcing partners and other external partners and therefore have a significant impact on country-level customer relationships. You will make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, oversight and supervision of the Country Research Director. 

Qualifications

What do you need to have?

  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse).
  • Experience in Oncology research preferred
  • BS/MSc level - 8-10 years of clinical research experience required with at least 4 years’ experience being in clinical trial management (managing complex or global trials preferred); 2+ years monitoring experience preferred.
  • MD/PhD level - 3-6 years of clinical research experience required in the clinical trial managment space. 
  • English fluency (ability to read, write, speak); fluency in host country language required
  • Experience in managing all trial components (start-up to database lock) 
  • Experience of clinical trial planning, (site) management and metrics
  • Experience identifying problems, conflicts and opportunities early and lead, analyses and prepare mitigation plans and drive conflict resolution


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

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