Clinical Systems Project Manager

Location: Nottingham, UK

Notice

This position is no longer open.

Requisition Number: 4271

Position Title: Clinical Systems Project Manager

External Description:

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of almost 2,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. 

What you will do 

  • Plan project scope and timelines to ensure successful delivery by defining scope deliverable in shorter timelines (thereby breaking larger scope efforts into multiple smaller phased projects), by ensuring the availability of all necessary participants, and by identifying risks and corresponding mitigation plans
  • Continuously assess project status, reassess and revise risks, oversee issue documentation and escalation, and ensure the project team and stakeholders remain informed of project status, risks, and issues throughout the project (including both periodic project health updates as well as ad hoc communications for emerging impacts)
  • Review and provide approval for project documents authored by other project team members or vendors, ensuring alignment with project objectives, Worldwide SOPs, and regulatory requirements
  • Request, receive and process/upload draft and final subject and kit schedules and inventory release files where required for projects that include study IRT delivery

What you will bring to the role

  • Ability to communicate concisely and effectively in both written and spoken English with proficient client-facing skills
  • Self-motivated individual who can positively contribute to a team environment
  • High attention to detail
  • Ability to prioritize and handle multiple projects simultaneously and make effective decisions in a fast-paced, highly dynamic environment
  • Flexible and able to use sound independent judgment and take initiative to assess information
  • Able to be creative, adapt to new technologies, concepts and processes, make improvements and solve problems

Your background 

  • Experience working in regulated environments such as clinical trials (GAMP, ISO Standards) in a Contract Research Organization (CRO) or Pharmaceutical environment
  • Familiar with IRT topics, including IRT study design, randomization methodologies, and just-in-time drug supply
  • Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations
  • Proven ability to manage delivery of technology solutions deployed in clinical trials – such as IRT, RTSM, CTMS, EDC or other relevant technologies desired
  • Familiarity with GxP Validation Requirements

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.   

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers! 

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Employment Type: Regular

Community / Marketing Title: Clinical Systems Project Manager

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: Nottingham, GB

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 Worldwide Clinical Trials does not accept unsolicited resumes from 3rd party vendors

© Worldwide Clinical Trials 2023

We only accept resumes from staffing organizations with pre-approved contractual agreements. Please do not forward resumes directly to our hiring managers, jobs alias, or any other company location. Unsolicited resumes from employment agencies will not be considered and Worldwide is not responsible for any fees related to unsolicited resumes.