PRAHS

Returning Candidate?

2017-43926

2017-43926

Title 
Senior Study Manager - Oncology New Indications - Home Based
Job Locations 
-
US-Remote
Canada-Remote
Posted Date 
12/1/2017

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 14,000+ 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 lifesaving 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.

The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.

Responsibilities

What will you be doing?

You will be in a coordinator/support role for the operational execution of a clinical protocol.  Assists the Program Lead and protocol team with the conduct of clinical studies. May have specific responsibilities for a single study or across multiple studies (e.g., data management deliverables, clinical supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines and will be proficient in project management tools. Shares technical expertise with team members. May interact with
internal and external stakeholders (study sites, vendors, committees, etc) in support of clinical study objectives.

Qualifications

  • A graduate degree or undergraduate degree.
  • Bachelor’s degree in the Life Sciences highly preferred
  • Study Manager level = BS with 4+ years’; or MS with 3+ years’; or PhD with <2 years’ relevant career experience
  • Senior Study Manager level = BS with 7+ years’; or MS with 5+ years’; or PhD with <2 years’ relevant career experience
  • Oncology experience required
  • Pharmaceutical and/or clinical drug development experience.
  • Excellent oral (including presentation) and written communication, computer/database management and project management skills

This is a home based position anywhere in the US or Canada



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

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