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
Monitor psychiatric and CNS trials at investigative sites across the Central United States. Support site startup, compliance, data quality, and study closeout at Worldwide Clinical Trials.
Apraksts
- Oversee clinical research at sites participating in Worldwide studies.
- Evaluate potential research sites for study participation.
- Coordinate study startup, including regulatory documents and contract and budget processes.
- Conduct PSSVs, SIVs, IMVs, and COVs.
- Train site staff on protocols, data collection, and safety reporting.
- Track site performance and assist with ongoing study activities.
- Verify informed consent, safety reporting, and regulatory compliance.
- Work with sites and study teams to maintain data quality, participant safety, and study progress.
- Help sites complete closeout activities and remaining study requirements.
Prasības
- Bachelor’s or nursing degree.
- At least five years of experience as a regional or traveling Clinical Research Associate.
- Experience monitoring CNS and psychiatric clinical trials.
- Travel within the assigned region, with 8–10 days on site per month.
- Full-service monitoring experience preferred.
- Strong knowledge of clinical trial processes, site management, and regulatory requirements.
- Must reside within the Central United States territory.
Priekšrocības
- Benefits package varies by location.
- Transparent compensation and pay equity.