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Clinical Research Associate - Cardiovascular, /Nash - West Coast

Employer
Worldwide Clinical Trials - USA
Location
California, United States;Homeworking
Salary
Competitive
Start date
11 Jan 2022
Closing date
8 Feb 2022

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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.

What Clinical Operations Site Management does at Worldwide

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can’t get anywhere else, with a team unlike anyone else.

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 trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.

What you will do
  • Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly late phase (II-III).
  • Conduct all types of visits - site qualifications, initiation, monitoring, site management and close out visits.
  • Ensure adherence and compliance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs)
  • Assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel

What you will bring to the role
  • Excellent interpersonal, oral, and written communication skills in English
  • Superior organizational skills with attention to details
  • Ability to work with little or no supervision
  • Proficiency in Microsoft Office, CTMS and EDC Systems


Your experience
  • Bachelor’s Degree, (RN plus experience may be considered in lieu of a bachelor’s degree)
  • 2+ years’ regional CRA experience for as a Clinical Research Associate
  • Experience in Cardiovascular, NASH required
  • Ability to meet the travel requirements of the job. Our metrics are 6-8 days on site per month.

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.

#LI-MM2
#LI-Remote

#CV

#NASH

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

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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