Principal Investigator, Psychiatrist (Staten Island)
il y a 2 jours
New York
Job Description Principal Investigator (BoardCertified Psychiatrist) - Staten Island, NY Full-Time * Onsite (5 days/week) Clinical Research Site Company Overview We are a nationally recognized clinical research organization with 20+ sites across the United States. Our multisite network conducts Phase I-IV clinical trials for leading biopharma partners, supported by dedicated clinical units, advanced safety infrastructure, and experienced research staff. Physicians here work at the forefront of innovation, contributing to therapies that improve outcomes for patients living with psychiatric and neurologic conditions, while operating in a collaborative, professionally run, and patientcentered environment. Position Summary We are seeking a BoardCertified Psychiatrist to serve as Principal Investigator (PI) at our Staten Island research site. The PI provides medical and scientific oversight for clinical trials, ensures participant safety, and upholds protocol and regulatory compliance. This role is 100% onsite, Monday-Friday. Only candidates who meet ALL of the following will be considered: • BoardCertified Psychiatrist, • Active, unrestricted New York MD license, • Ability to commute to Staten Island five days per week If you do not meet all three requirements, please do not apply. Key Responsibilities Clinical Oversight • Serve as Principal Investigator for assigned clinical trials, providing medical leadership and oversight., • Conduct psychiatric evaluations and diagnostic assessments., • Assess subject eligibility and compliance with investigational product and scheduled visits., • Evaluate participant responses to therapy and manage adverse events in accordance with protocol., • Maintain complete familiarity with all investigational product(s) used in assigned studies. Protocol Planning & Execution • Collaborate with the Site Director, Study Coordinator, and Recruitment Manager to support enrollment planning and execution., • Ensure staff are trained and operating in compliance with SOPs, GCP, and protocol requirements., • Confirm that the site maintains adequate staffing, resources, and facilities needed for successful study conduct., • Maintain an uptodate curriculum vitae and all required training and certification files. Regulatory Compliance • Promote adherence to FDA regulations, ICHGCP guidelines, and company SOPs., • Document protocol deviations, unanticipated issues, and any premature unblinding events., • Communicate promptly with IRBs, sponsors, and internal teams as required., • Ensure accurate, complete, and auditready clinical trial documentation. Leadership & Staff Mentorship • Provide oversight, guidance, and mentorship to SubInvestigators., • Review SubInvestigator work to ensure adherence to protocols and regulatory standards., • Foster a productive, professional, and compliant work environment for clinical staff. Communication & Collaboration • Communicate professionally with subjects, research staff, sponsors, CROs, and IRBs., • Provide updated information regarding study progress, investigational products, and protocol procedures., • Assist with rating scales and structured clinical assessments as required. Required Qualifications (NonNegotiable) • Board Certification in Psychiatry (ABPN), • Active, unrestricted New York State medical license (MD), • Ability to work onsite in Staten Island, NY, Monday-Friday, • Excellent clinical judgment and psychiatric diagnostic skills, • Strong understanding of medical terminology, clinical workflows, and patientsafety oversight, • Professional written, verbal, and interpersonal communication skills, • Ability to collaborate effectively within a multidisciplinary clinical research team Preferred Qualifications • Prior experience as a Principal Investigator or SubInvestigator (not required but preferred), • Familiarity with GCP, ICH guidelines, and clinical trial operations, • Experience interacting with sponsors or participating in study placement activities, • Experience with psychiatric rating scales or structured clinical assessments, • Ability to adapt to shifting priorities and fastpaced research timelines, • Strong organizational, leadership, and problemsolving abilities, • Proficiency with EMR systems, Word, Excel, and clinical research software Work Environment • Onsite clinical research facility with dedicated support staff, • Monday-Friday daytime schedule, • Collaborative environment focused on quality, compliance, and patient safety, • No nights, weekends, or oncall responsibilities Compensation & Benefits • Competitive compensation based on experience, • Medical, dental, and vision benefits, • Matching 401(k), • Paid time off and holidays, • Opportunities for training and professional development Company DescriptionA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints. Job Responsibilities: -\tConducting Post Market Activities and Post Market Surveillance -\tManaging Customer and Product Complaint Investigation programs Education and Experience: -\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry -\tBachelor's degree -\tComputer proficiencyA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints.\r\nJob Responsibilities:\r\n•\tConducting Post Market Activities and Post Market Surveillance\r\n•\tManaging Customer and Product Complaint Investigation programs\r\nEducation and Experience:\r\n•\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry\r\n•\tBachelor's degree\r\n•\tComputer proficiency