Worldwide Clinical Trials ir globāla līgumizpētes organizācija, kas atbalsta farmācijas un biotehnoloģiju uzņēmumus visā zāļu izstrādes ciklā. Ar vairāk nekā 30 gadu pieredzi uzņēmums nodrošina klīnisko pētījumu uzraudzību, datu pārvaldību, pacientu piesaisti un konsultācijas regulējuma jautājumos tādās terapeitiskajās jomās kā onkoloģija, kardioloģija un retās slimības. Tā pieeja apvieno plašu klīnisko pētījumu pieredzi ar personalizētu atbalstu un sarežģītiem pētījumiem pielāgotiem risinājumiem.
Senior Clinical Research Associate, Psychiatry
Lead monitoring and site support for psychiatric clinical trials across the East Coast with Worldwide Clinical Trials. The role covers site selection, study start-up, compliance, data quality, and participant safety.
Apraksts
- Oversee clinical research at sites participating in Worldwide studies
- Evaluate prospective research sites
- Coordinate study start-up, including regulatory documents, contracts, and budgets
- Conduct pre-selection, initiation, interim monitoring, and closeout visits
- Train site staff on protocols, data collection, and safety reporting
- Track site performance and provide ongoing study support
- Maintain informed consent, safety reporting, and regulatory compliance
- Work with sites and study teams to support data quality, participant safety, and study delivery
- Help sites close out and complete study requirements
Prasības
- Bachelor’s or nursing degree
- At least five years’ experience as a regional, traveling Clinical Research Associate
- Experience monitoring psychiatric clinical trials
- Travel within the assigned region, averaging 8–10 days per month
- Full-service monitoring experience preferred
- Strong understanding of clinical trial processes, site management, and regulatory requirements
- Reside within the East Coast United States territory
Priekšrocības
- Benefits package varies by location
- Inclusive and equitable workplace
- Transparent compensation and pay equity