Worldwide Clinical Trials
Worldwide Clinical Trials
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 and Alzheimer’s

Monitor psychiatry and Alzheimer’s clinical trials for Worldwide Clinical Trials across East Coast sites. Oversee site visits, regulatory compliance, and data quality.

Apraksts

  • Oversee clinical research at investigative sites taking part in Worldwide studies.
  • Find and evaluate prospective research sites.
  • Coordinate study start-up, including regulatory documents and contract and budget processes.
  • Conduct site selection, study initiation, interim monitoring, and closeout visits.
  • Prepare site staff on protocol requirements, data collection, and safety reporting.
  • Track site performance and help maintain study activities.
  • Check that informed consent, safety reporting, and regulatory requirements are met.
  • Work with sites and study teams to support data quality, participant safety, and study progress.
  • Help sites close out studies and complete required activities.
  • Coordinate with sites, sponsors, and global study teams.

Prasības

  • Bachelor’s degree or nursing degree.
  • At least five years of experience as a regional or traveling Clinical Research Associate.
  • Experience monitoring psychiatry or Alzheimer’s clinical trials.
  • Travel within the assigned region, approximately 8–10 days of site visits per month.
  • Full-service monitoring experience is preferred.
  • Strong understanding of clinical trial processes, site management, and regulatory requirements.
  • Must live within the East Coast territory.
  • Ability to travel to investigative sites approximately 8–10 days per month.

Priekšrocības

  • Benefits package varies by location.
  • Inclusive and equitable workplace.
  • Transparent compensation and pay equity.