Psychologist - Clinical Research Site
7 days ago
Los Angeles
Job Description Position Summary The Psychologist will provide psychological assessments, therapeutic support, and research-related evaluations for participants enrolled in clinical trials. This role ensures accurate data collection, participant well-being, and adherence to study protocols and ethical standards. Key Responsibilities • Participant Assessment, • Conduct psychological evaluations to determine eligibility for clinical trials., • Administer and score standardized psychological tests and rating scales (e.g., MMPI, HAM-D, BDI)., • Document baseline and follow-up mental health status per protocol requirements., • Therapeutic Support, • Provide counseling or supportive therapy to participants as permitted by the study design., • Monitor participant well-being and intervene in cases of psychological distress., • Maintain confidentiality and ethical standards in all interactions., • Protocol Compliance, • Ensure all assessments and interventions adhere to the study protocol and Good Clinical Practice (GCP)., • Accurately record data in source documents and electronic data capture systems., • Assist in preparing documentation for audits and inspections., • Safety Monitoring, • Identify and report adverse psychological events promptly to the research team., • Collaborate with medical staff to address participant safety concerns., • Implement risk mitigation strategies for vulnerable participants., • Collaboration, • Work closely with principal investigators, psychopharmacologists, and research coordinators., • Participate in team meetings to review participant progress and protocol updates., • Communicate effectively with participants about study procedures and expectations., • Education & Training, • Educate participants on the purpose of psychological assessments and confidentiality., • Provide guidance to staff on psychological testing and participant engagement., • Data Integrity, • Ensure accuracy and completeness of psychological data collected during the trial., • Maintain compliance with IRB, FDA, and sponsor requirements. Qualifications • Doctoral degree (Ph.D. or Psy.D.) in Clinical Psychology., • Licensed Psychologist in [State]., • Experience in clinical research or clinical trial settings preferred., • Knowledge of GCP, IRB regulations, and ethical standards., • Strong assessment, documentation, and communication skills. Skills • Expertise in psychological testing and interpretation., • Ability to manage participant distress and maintain rapport., • Detail-oriented with a commitment to data accuracy and regulatory compliance.Company DescriptionThe Concierge Clinical Trials Medical and Scientific team boasts exceptional experience and expertise across the full spectrum of clinical trials and their crucial role in drug development. Led by Dr. Neal Cutler, the former CEO and founder of Worldwide Clinical Trials, and his core team members, this dedicated group has over 30 years of experience conducting hundreds of clinical trials involving thousands of patients. Dr. Cutler and his key members successfully expanded Worldwide Clinical Trials to a robust workforce of over 3,200 employees. Additionally, they played a pivotal role in establishing California Clinical Trials as the largest single-site clinical research facility in the United States. Their work spans virtually to all therapeutic areas, including endocrinology, cardiology, oncology, psychiatry, and neurology. This includes early first-in-man studies with novel study designs (including invention of the Bridging Study and CSF-continuous sampling studies) to critical decision-making single-site Phase 2 studies, to participation in large-scale pivotal Phase 3 and post-marketing trials. Concierge Clinical Trials scientific expertise is showcased by over 300 publications, including a dozen books and numerous book chapters, and membership in important scientific societies such as the American Society for Clinical Pharmacology and Therapeutics, where new groundbreaking data has been presented over the years. Renowned for their expertise, the medical team is frequently sought for scientific guidance across all phases of trials and therapeutic areas.The Concierge Clinical Trials Medical and Scientific team boasts exceptional experience and expertise across the full spectrum of clinical trials and their crucial role in drug development. Led by Dr. Neal Cutler, the former CEO and founder of Worldwide Clinical Trials, and his core team members, this dedicated group has over 30 years of experience conducting hundreds of clinical trials involving thousands of patients. Dr. Cutler and his key members successfully expanded Worldwide Clinical Trials to a robust workforce of over 3,200 employees. Additionally, they played a pivotal role in establishing California Clinical Trials as the largest single-site clinical research facility in the United States. Their work spans virtually to all therapeutic areas, including endocrinology, cardiology, oncology, psychiatry, and neurology. This includes early first-in-man studies with novel study designs (including invention of the Bridging Study and CSF-continuous sampling studies) to critical decision-making single-site Phase 2 studies, to participation in large-scale pivotal Phase 3 and post-marketing trials.\r\n\r\nConcierge Clinical Trials scientific expertise is showcased by over 300 publications, including a dozen books and numerous book chapters, and membership in important scientific societies such as the American Society for Clinical Pharmacology and Therapeutics, where new groundbreaking data has been presented over the years.\r\n\r\nRenowned for their expertise, the medical team is frequently sought for scientific guidance across all phases of trials and therapeutic areas.