Senior Study Manager - Oncology - Home Based
Pra Health Sciences
20h ago

What will you be doing?

You will be accountable for the operational planning, feasibility, and execution of a clinical protocol. You may lead a team in key study planning, development and execution elements (e.

g., data management deliverables, protocol level plans / timelines, country / site selection, system updates, Investigator Meeting planning, communication plans, preparation of status update reports, study closeout activities).

You may serve as the clinical trial team (CTT) lead for timeline management, risk identification and mitigation, issue resolution.

You will be accountable for managing any study specific partners and / or vendors. You will also facilitate and collaborate with key internal / external stakeholders (study team, subsidiary country teams, vendors, committees, etc) in support of clinical study objectives.

What you need to have :

  • 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
  • Senior Study Manager level BS with 7+ years’; or MS with 5+ years’; or PhD with
  • Oncology experience required
  • Pharmaceutical and / or clinical drug development experience.
  • 20-30% travel required
  • Excellent oral (including presentation) and written communication, computer / database management and project management skills
  • 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.
  • This is a home based position anywhere in the US or Canada

    Add to favourites
    Remove from favourites
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form