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 — North Carolina Remote
Monitor CNS and psychiatric clinical trials for Worldwide Clinical Trials, a global CRO. Oversee site management, regulatory compliance, data quality, and regional travel.
Apraksts
- Oversee clinical research at investigative sites in Worldwide Clinical Trials studies
- Evaluate prospective research sites
- Coordinate study start-up, 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 provide ongoing study support
- Ensure proper informed consent, safety reporting, and regulatory compliance
- Work with sites and study teams to support data quality, participant safety, and study delivery
- Assist with site closeout and completion of study requirements
- Travel to investigative sites about 8–10 days each month
Prasības
- Bachelor’s or nursing degree
- More than five years’ experience as a regional, traveling Clinical Research Associate
- Experience monitoring CNS and psychiatric clinical trials
- Availability to travel within the assigned region for 8–10 days each month
- Full-service monitoring experience preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
- Must live within the Central United States territory
Priekšrocības
- Benefits package varies by location
- Inclusive and equitable workplace
- Transparent compensation and pay equity