Worldwide Clinical Trials yra pasaulinė sutartinių klinikinių tyrimų organizacija, padedanti farmacijos ir biotechnologijų įmonėms viso vaistų kūrimo ciklo metu. Daugiau nei 30 metų patirtį turinti įmonė teikia klinikinės stebėsenos, duomenų valdymo, pacientų įdarbinimo ir reguliavimo konsultavimo paslaugas tokiose terapinėse srityse kaip onkologija, kardiologija ir retosios ligos. Jos požiūris derina plačią klinikinių tyrimų kompetenciją su individualia pagalba ir sudėtingiems tyrimams pritaikytais sprendimais.
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.
Aprašymas
- 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.
Reikalavimai
- 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.
Privalumai
- Benefits package varies by location.
- Transparent compensation and pay equity.