Alina Goldstein

• Utilized critical thinking skills to prioritize nursing interventions based on patients'' acuity levels and individual needs.
• Conducted thorough patient assessments to identify changes in condition, promptly notifying physicians and initiating appropriate interventions when necessary.
• Administered medications safely according to established guidelines while closely monitoring for side effects or adverse reactions requiring intervention.
• Enhanced patient satisfaction by providing compassionate, holistic nursing care that addressed physical, emotional, and spiritual needs.
• Assisted in the training and mentorship of new nursing staff members, contributing to a positive work environment and high-quality patient care.
• Improved patient outcomes by implementing evidence-based nursing interventions and individualized care plans.
• Provided support for patients'' families during difficult medical decisions or end-of-life care, serving as a liaison between the healthcare team and loved ones.
• Advised patients and caregivers of proper wound management, discharge plan objectives, safe medication use, and disease management.

• Provide day-to-day operational leadership to assigned specialty program area(s) and maintain a demeanor of innovative professional leadership, civility, teamwork while undertaking all tasks and interactions. Participate in unit-based committees, staff meetings and other groups in assigned unit(s) service area on patient care.
• Provide oversight of clinical staff and patient care to include, staffing, orientation, education, policy/process compliance and overall quality of patient interaction and care. Interviewed, hired and trained new employees. Perform annual performance evaluations, unit competencies and orientation checklists for assigned employees.
• Encourage and develop risk, quality and safety reporting and analysis to foster problem solving, root case analysis for operational and clinical improvement. Educate staff on clinical care of patients (patient population specific, generalized care, equipment, workflows, documentation, etc.). Strictly followed study sponsor rules and regulations, prepared reports and monitored study medication distribution and daily medications.
• Exhibit responsibility for ensuring appropriate policies, procedures and documentation are utilized by assigned area(s). Participate in development and concurrent review of policies

and procedures. Assures appropriate staff training for new procedures. Strictly follow state and federal regulations.

• Monitor assigned area(s) productivity standards. Assists leadership with operational and capital budget development and fiscal oversight. Assists leadership and materials management to assure appropriate equipment and supplies are available. Provide input on supply use and supply/equipment cost analysis.
• Proactively partner with Human Resources in areas of employee relations, corrective action, performance management, recruiting, compensation, benefits and HR policies. Work closely with HR to develop job descriptions and job standards for each position and monitor for accuracy. Conduct performance appraisals according to HR guidelines. Provide regular, scheduled feedback to assigned employees regarding performance. Establish processes to ensure employees are properly trained for positions and develops cross training opportunities as warranted.
• Developed positive work culture with strong emphasis on collaboration, innovation, and continuous improvement.
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• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Collected data and followed research protocols, operations manuals and case report form requirements.
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
• Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
• Followed informed consent processes and maintained records.
• Gathered, processed and shipped lab specimens.
• Collected, evaluated and modeled collected data.
• Coordinated clinical trials focused on disorders such as Anxiety,MDD,Alzheimer,Insomnia,Migraine,OCD,Insomnia with Alcohol Cessation and Schizophrenia.
• Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.

• Assisted with regulatory binders and quality assurance and quality control procedures.
• Performed administrative support duties.
• Maintained research data, participant fields, regulatory binders and study databases.
• Obtained participant study data from records.
• Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.