Clinical Study Manager Associate

Location: San Antonio, Texas, United States

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Requisition Number: 4622

Position Title: Associate Clinical Study 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.

 

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.

 What you will do:

The Associate Clinical Study Manager will support the Clinical Study Manager (CSM) on one or more allocated Phase I through IV Clinical Trials that may be local, regional, or global in scope. The Associate Clinical Study Manager will support the overall coordination and management of clinical trials from start up through close out activities.

 

The Associate Clinical Study Manager responsibilities include, but are not limited to, the following:

  • Review and provide follow-up correspondence to study monitor reports.
  • Assist in providing study updates to sponsors.
  • Assist in tracking and maintenance of project related information.  Set up initial new study in Clinspark and communicate to team accordingly.
  • Provide varying support across multiple projects.

 

What you will bring to the role

  • Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment, Strong attention to detail, Strong organizational skills, Knowledge and understanding of ICH, GCP, FDA regulations
  • Self-motivated and excellent problem-solving skills, strong interpersonal skills, ability to work independently
  • Must be able to work effectively with co-workers in a team environment and individually unsupervised.  Must be able to perform duties at a fast pace without errors.

 Your experience:

  • Bachelor’s Degree (preferably in the field of Life Sciences or Health) with clinical research experience
  • or Associates Degree and an accredited Clinical Research credential, or 5 years of clinical research experience in lieu of a degree.

 

City:

State:

Employment Type: Regular

Community / Marketing Title: Clinical Study Manager Associate

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: San Antonio, Texas US

CountryEEOText_Description: Worldwide Clinical Trials is an equal opportunity employer, dedicated to a policy of non-discrimination in employment on any basis including age, sex, color, race, creed, national origin, religion, marital status, sexual orientation, political belief or disability.

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

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© Worldwide Clinical Trials 2021

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.