Requisition number 3484 employment type: regular
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 excellenceWe are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences cros, in the best possible way.
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 trialsExcellent oral and written communication skills, time management, and organizational skills are vital to this positionWhile this role is work-from-home, candidates must able come into the office in 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 cra experience
Willingness to travel required
Worldwide clinical trials is an equal opportunity employer
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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.
