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Risk Manager

Employer
Worldwide Clinical Trials - USA
Location
United States;Homeworking
Salary
Competitive
Start date
28 Sep 2022
Closing date
26 Oct 2022

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Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

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 over 3,000 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

As a Risk Manager, you will coordinate cross-functional risk management and central monitoring activities for assigned clinical trials in accordance with monitoring in accordance with ICH GCP E6 requirements. Will assist in the maintenance of the risk library and provide guidance to ensure consistency within programs, therapeutic areas and/or sponsors.

RESPONSIBILITIES:
Some team members may focus on a limited number of these responsibilities depending on requirements. Tasks may include but are not limited to:
Serves as the Risk Management Lead within the assigned project team:

  • Understands the study scope of work, budget and protocol content for their assigned trial.
  • Provides subject matter expertise for the development and maintenance of the monitoring strategy required for the trial.
  • As required, develops and delivers training to the study team regarding the risk assessment, centralised monitoring and the wider monitoring strategy.
  • Drafts initial risk assessment and supports the project team in finalising the Risk Planning Tool, ensuring cross functional involvement.
  • Develops the RMP for the assigned study and gains GPL and Sponsor approval. May provide advice on the development of functional plans.
  • Supports the GPL in ensuring compliance with cross-functional review of risks throughout the trial.
  • Ensures Inspection Readiness for risk assessment and centralized monitoring scope.
  • Maintains the Risk Library.
  • When required, will conduct study level review of KRIs/KPIs or statistical monitoring.
  • With support and where required, collaborates with other team members and Sponsor to identify and track trial level Quality Tolerance Limits.



OTHER SKILLS AND ABILITIES:
  • Excellent communication, presentation and interpersonal skills.
  • Excellent planning and organizational skills with effective time management
  • Excellent interpersonal skills
  • Knowledge of clinical project financial principles
  • Ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identify and mitigating potential threats to the successful conduct a clinical research project.
  • Ability to lead and motivate assigned team (if applicable)
  • Ability to provide experience and input into process initiatives and development relating to monitoring and site management activities
  • Proficiency in Microsoft Office


REQUIREMENTS:

  • BSc/RN or equivalent combination of knowledge, skills and experience
  • At least 8 years knowledge and prior experience of Risk Based Monitoring and associated ICH/Regulatory guidance required. Experience as a Risk Manager, preferred.
  • Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues.
  • Demonstrated ability to lead and align teams in the achievement of project milestones, as well as demonstrated capability of working in global environment.

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!

#LI-HD1

#LI-Remote

Company

Find out more about working for our company

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Brief Company Description; 

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 over 2,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Company info
Mini-site
Worldwide Clinical Trials - USA
Location
600 Park Offices Drive
Suite 200
Research Triangle Park
NC 27709
United States

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