Time organization is seeking a research student to join our team for psychiatric studies under the guidance of a renowned psychiatrist, Dr. Padder.
Qualifications:
Bachelor or master’s level psychology student:
• Interest and experience in research, preferably clinical trials
• Proficiency in data management and analysis software •
· Knowledge of clinical trial phases, research methodologies, and regulatory requirements, including IRB protocols and Good Clinical Practice (GCP) guidelines is preferable •
· Strong organizational and multitasking abilities •
· Excellent communication and interpersonal skills
Key Responsibilities:
• Coordinate Research Activities:
• Support clinical research studies and ensure a safe environment as directed by the Principal Investigator.
• Assist the Principal Investigator and Clinical Research Associate (CRA) in managing the research protocols and ensuring compliance with IRB requirements. •
• Administer rating scales and participate in cutting-edge Phase 2 and 3 research projects.
• Study Documentation and Data Management:
• Maintain protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other documents up to date.
• Assist with data entry, quality checking, and query resolution to ensure protocol adherence and data accuracy. • Logistics and Preparation: Plan and manage logistical activities for study procedures following the study protocol.
• Prepare for clinical studies by labeling specimen collection tubes, inventorying supplies, and setting up or troubleshooting equipment. •
• Volunteer Recruitment and Management: Recruit, screen, and orient volunteers for study enrollment according to the protocol. Ensure proper custody and management of the study drug as per site procedures. •
• Coordinate with the study monitor and respond to their questions effectively.
How To Apply:
Email resume and cover letter to Shareese Kess, LCSW-C, CCM @ skesslewis@timeorganization.org
This internship is eligible for Experiential Learning Credit. https://go.umd.edu/psyc389
