Das ist der Job
Responsibilities Manage research activities at sites participating in Worldwide’s clinical projects.
Darum lohnt es sich
We believe diverse backgrounds and teamwork enable professionals to succeed and help improve lives through innovative pharmaceutical development. Our team works with regulatory submissions, TMF management, and site-related activities, with strong emphasis on development, coaching, and a clear career path toward management roles.
Overview
Worldwide Clinical Trials is a global midsize CRO focused on advancing clinical research with a collaborative, inclusive culture. At Worldwide Clinical Trials, Clinical Operations drives the execution of clinical studies across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Participate in all stages of the clinical study, including site identification, start-up activities, regulatory documentation collection, and contract and budget negotiation. Train sites to collect data properly and report safety-related events.
Manage site activities during study maintenance and close-out research activities after study completion. Conduct study initiation visits (SIVs). Work primarily remotely while ensuring compliance with informed consent, safety reporting, and applicable regulatory requirements.
What you will bring to the role Excellent interpersonal, oral, and written communication skills in Engli
