Worldwide Clinical Trials is seeking a Clinical Research Associate to manage research activities at clinical sites, predominantly registries and observational studies. You will identify sites, support regulatory tasks and contracts, and train sites to collect data accurately while reporting safety events.
The role involves performing study initiation visits (SIVs) and ensuring informed consent compliance, with travel as required and collaboration across global teams.
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Senior Clinical Research Associate – Remote Site Leadership employer: Worldwide
At Worldwide Clinical Trials, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. Our remote work model allows for flexibility while our commitment to diversity and inclusion ensures that every team member can thrive and contribute meaningfully to our mission of improving lives. With ample opportunities for professional growth and a supportive environment, we empower our employees to take charge of their careers and make a real impact in the clinical research field.
