Clinical Research Associate - Phase I (San Antonio, TX)

Multiple Locations: San Antonio, TX, USA • Dallas, TX, USA • Fort Worth, TX, USA • Austin, TX, USA • Texas, USA

Notice

This position is no longer open.

Requisition Number: 2302

Position Title: Clinical Research Associate II

External Description:

The Clinical Research Associate (CRA) is responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
 
Successful candidate will be experienced in Phase I trials. Excellent oral and written communication skills, time management, and organizational skills are vital to this position. While this role is work-from-home, candidates must be local to San Antonio, Texas. 

REQUIREMENTS:

  • Bachelor degree, or a two-year degree in nursing, is required
  • Minimum of 2 years monitoring experience required
  • Must have previous Phase I experience
  • Willingness to travel required
  • Valid current passport required

Worldwide Clinical Trials is an Equal Opportunity Employer

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City:

State: Texas

Employment Type: Contractor

Community / Marketing Title: Clinical Research Associate - Phase I (San Antonio, TX)

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 is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.

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© 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.