Clinical Psychosis Specialist

Transforming Addiction and Neurological Care with AIOur organization is dedicated to developing innovative AI digital health and medical device platforms, focusing on addiction, psychosis, neurological disorders, and pain management. As a key member of our team, you will contribute to shaping the future of digital care by combining clinical expertise with AI...

Clinical Quality Assurance Compliance JobThe selected candidate will be accountable for Quality Compliance (QC) activities of the Clinical Trial Medical Science team, Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team.To ensure 24/7 Inspection/Audit Readiness, we review all study-related activities, processes,...

Job Title:Offshore Clinical Systems TesterJob DescriptionWe are seeking a skilled Offshore Clinical Systems Tester to support testing and validation activities within a Decentralized Clinical Trial environment. The ideal candidate will have strong expertise in Veeva CDMS (EDC), hands-on experience with eCOA and IRT platforms, and excellent documentation and...

Job Summary:The Central Monitoring Strategist plays a pivotal role in ensuring data integrity, patient safety, and operational excellence across clinical development programs through advanced centralized monitoring and risk-based quality management.Design comprehensive risk-based quality management (RBQM) plans tailored to each study's needs.Conduct thorough...

Job Title: Clinical Admin Associate">"> Medical scribes, hospital admin, pharmacy back-office, RCM/claims back-office, clinic coordinators.">">"> This is a repetitive role in our organization handling templated clinician/clinic communications, records hygiene, and daily logs. No calls. No sales. Confidentiality first."> Execute templated, high-volume...

**Job Summary**This is a full-time contract role offering 30–40 hours per week of consistent work.The QA Specialist will act as a core member of the quality assurance function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.Key ResponsibilitiesServe as primary QA support resource for clinical study teamsProvide...

Job Title: Clinical Research AssociateAbout the Role:We are seeking a highly skilled and experienced Clinical Research Associate to join our team. The ideal candidate will have a strong background in clinical research, with expertise in protocol development, informed consent forms, and regulatory compliance.The successful candidate will be responsible for...

Delivering exceptional outcomes as a Clinical Research Associate demands a unique blend of scientific acumen, organizational prowess, and interpersonal finesse.In this pivotal role, you will be instrumental in coordinating on-site trial activities under the guidance of experienced professionals.Your primary responsibilities will include maintaining...

Medical Scribing RoleAs a Medical Scribe, you play a vital part in preparing and finalizing reports for patient exams.This is an opportunity to work closely with US-based physicians, assisting them with their day-to-day tasks and helping to reduce work volume by documenting non-clinical report portions.

Job DescriptionThe ideal candidate will possess excellent writing skills and a thorough understanding of clinical trial regulations.Developing Key Clinical Trial Documents:Protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs)Translating Complex Scientific Data:Clear, regulatory...