AstraZeneca

Senior Clinical Project Manager - CVRM/RIA

5 days left

Location
England
Salary
Negotiable
Posted
30 Aug 2019
Closes
20 Sep 2019
Ref
R-060042
Contact
AstraZeneca
Hours
Full Time
Contract Type
Permanent
Experience Level
Management

Senior Clinical Project Manager - CVRM/RIA

Due to our promising pipeline and the growth of our EarlyClinical Operations team, we have several new positions open for Senior Clinical Project Managers (CPMs.) These roles are full-time office-based positions and can be based in our Cambridge UK office, Gaithersburg, US office or Gothenburg, Sweden office .

Working on a strong pipeline means so much more than producing innovative, ground-breaking medicines. It allows AstraZeneca people to be part of long-term development programs with the variety that comes from working at the leading edge of science and technology.

Are you passionate about working in a collaborative environment with a high-potential pipeline?

Role

As a Senior Clinical Project Manager, you will plan and lead overall clinical operations for assigned clinical trial(s)/projects. You will be responsible for timelines, budgets, resources, investigational sites, vendors and key project deliverables in compliance with SOPs, Regulatory standards and ICH/GCP guidelines and in alignment with the CVRM Therapeutic Area (TA) strategies and goals. You will provide matrix management of functional area representatives to cross-functional clinical trial teams (CTTs).

Responsibilities

As a Senior CPM you will be the orchestrator and centre of running global clinical trials. You will work cross- functionally across diverse global groups, interacting with scientific therapy areas to ensure successful delivery of high quality, cost efficient clinical studies. As part of this you will:

  • Convene, define and lead accountabilities for cross-functional teams
  • Develop, run and manage study timelines and budgets. Reporting risks and opportunities
  • Review, refine, and approve Clinical Operations Plans
  • Oversee adherence to pertinent regulations such as ICH/GCP
  • Lead ongoing review of data to ensure quality and consistency
  • Manage vendors throughout the life of assigned trial
  • Oversee the submission of trial-related and essential documents to the Trial Master File
  • Mentor staff and acts as a resource

Requirements

To succeed in this role, you will be able to demonstrate your established and progressive experience in clinical operations, and you will be an experienced Clinical Project Manager.

You will have:

  • Bachelor's Degree Required in a relevant scientific subject
  • Experience in clinical project management operations including project coordination, site management and monitoring or equivalent including project management experience or equivalent
  • Ability to lead a cross-functional team in a matrix environment
  • Proven complex problem solving and decision making skills
  • Strong leadership, communication, management and organizational skills, conflict resolution, and
  • Deep understanding of country level regulations, ICH and GCP guidelines
  • Ability and willingness to travel 25% of the time (internationally and domestically)

Next Steps - Apply today!

Closing date 26th September 2019

To be considered for this exciting opportunity, we ask you to complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.

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