Executive Director, Clinical Program Lead Insmed IncExecutive Director, Clinical Program LeadNJ$306,000–$417,000 / yearFor New York City Residents: To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. This role is a core member of the Global Project Team (GPT) and leads the Global Clinical Team, overseeing physicians and clinical scientists responsible for study design, execution, safety oversight, and supporting regulatory engagements.
MR Technologist and Safety Officer Columbia UniversityMR Technologist and Safety OfficerNY$80,000–$105,000 / yearReporting directly to the MR Managing Director, the Technologist/MRSO is responsible for day-to-day operations of two 3T Siemens MRI systems, supporting researchers by assisting with the execution of their studies, and for the maintenance and enforcement of safety policies, procedures, and training. Zuckerman Mind Brain Behavior Institute unites world-class scientists across diverse academic disciplines to conduct groundbreaking research that transforms our understanding of the brain and its influence on the mind and behavior.
Compliance and Training Coordinator Columbia UniversityCompliance and Training CoordinatorNew York, NY$72,000–$76,000 / yearAbility to work and communicate positively and effectively with researchers, veterinarians, and other CTSs; Strong knowledge of regulations and guidelines pertaining to the use of laboratory animals; Strong knowledge of laboratory animal science, including familiarity with all of the commonly used species of animals; Ability to work independently, with minimal supervision, in a fast-paced environment with frequently changing priorities; Keen attention to detail. The Compliance and Training Coordinator (CTC) reports to the Executive Director of the Office of the Institutional Animal Care and Use Committee (IACUC) and works closely with other staff members.
Senior Vice President, Medical Affairs TempusSenior Vice President, Medical AffairsNew York, NY$365,000–$475,000 / yearTempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. A knowledge base in molecular diagnostics, precision oncology, health systems, clinical research, and use of large data sets/real world data and medical communications is required.
Senior Manager/Associate Director, Clinical Pharmacology SystImmune, Inc.Senior Manager/Associate Director, Clinical PharmacologyPrinceton, NJ$150,000–$200,000 / yearThe ideal candidate will provide expertise in pharmacokinetics, dose optimization, pharmacometrics, and drug interaction assessment, collaborate with cross-functional teams (Clinical, Research, Regulatory, Biometrics, etc.), and manage clinical pharmacology studies, data analysis, and regulatory filings. Take a lead role in preparing and meticulously reviewing clinical pharmacology sections of study protocols, reports, investigators' brochures and regulatory filings (IND's, BLA's, etc.), and responds to regulatory inquiries related to clinical pharmacology.
Assistant Director Of Student Development And Campus Life Berkeley CollegeAssistant Director Of Student Development And Campus LifeNewark, NJ$57,000–$62,000 / yearBerkeley College is currently seeking an Assistant Director of Student Development and Campus Life (SDCL) to support the implementation of programs and initiatives designed to enhance student experience across all Berkeley College campuses. The Assistant Director plays a key leadership role in developing co-curricular programs, fostering student engagement, advising student organizations, and coordinating major departmental events.
Senior GCP Auditor (Good Clinical Practice Quality Assurance) Macpower Digital Assets Edge Private LimitedSenior GCP Auditor (Good Clinical Practice Quality Assurance)Paramus, NJ$48–$53 / hourJob Summary: This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting quality management systems to ensure compliance and minimize risk in a regulated pharmaceutical environment. Performs and manages all types of audits in the audit program of Clinical Development and Safety Pharmacovigilance Must Have: Bachelor's degree in a scientific, health care, or related discipline .
Drug Safety Physician SystImmune, Inc.Drug Safety PhysicianPrinceton, NJ$150,000–$250,000 / yearThis individual will also support the clinical R&D team in the oversight of PV service vendors and partners and will need to maintain medical knowledge, as well as current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Director/Sr. Director/Executive Director, Clinical Regulatory Affairs SystImmune, Inc.Director/Sr. Director/Executive Director, Clinical Regulatory AffairsPrinceton, NJ$200,000–$300,000 / yearThe Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department in all aspects of global regulatory affairs related to development of novel oncology therapeutics (multiple modalities such as ADCs, bispecific antibodies and T-cell engagers etc.). Own/drive the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: BLA/INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator's Brochure.
NewAssociate Director, Clinical Trial Lead Biogen IncAssociate Director, Clinical Trial LeadNY$162,000–$223,000 / yearThe best part: You will own responsibility for entire clinical trial studies, including operational design, successful delivery, and the positive impact on the lives of patients with a wide array of neurological conditions, including nephrotic conditions, multiple sclerosis (MS), Alzheimer's disease, and spinal muscular atrophy (SMA). Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
Immigration Staff Attorney New York County Defender ServicesImmigration Staff AttorneyNew York, NYFull timeJob Description and Responsibilities: Advise and strategize with our trial attorneys and clients to avoid negative immigration consequences; Provide immigration support to trial attorneys at arraignments; Present information to judges and assistant district attorneys through written or oral advocacy; Advocate for clients by conducting jail visits and accompanying clients to ICE appointments; Must be committed to working collaboratively with a diverse group of criminal defense attorneys and other advocates; Manage a high-volume caseload; Present in-office trainings on crim-imm basics and changes to crim-imm law; Attend IDP’s monthly roundtable meetings; Participate in other immigration coalition and organization meetings; and. Qualifications: Commitment to advancing the rights of poor and low-income immigrants; Commitment to criminal justice issues; Must be fluent in Spanish; Minimum of three years’ experience in immigration law, particularly as it intersects with criminal law; Excellent research, writing, analytical, interpersonal and communication skills; Strong organizational and time-management skills; Must be admitted to practice law in New York State;
Director Of Clinical Science - Hematology SystImmune, Inc.Director Of Clinical Science - HematologyPrinceton, NJ$180,000–$230,000 / yearAuthor components with the Medical Director and reviewer of clinical and regulatory documents and registration dossiers (i.e., protocol, ICF, IB, safety updates, study reports, regulatory submissions, etc.) to support registration and commercialization of the compound(s). SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
Medical Science Liaison, Nephrology - North Central U.S. (location in IL, MN, WI, MI, IN) Celgard, LLCMedical Science Liaison, Nephrology - North Central U.S. (location in IL, MN, WI, MI, IN)New York, New York$170,000–$207,000Identifies and conducts outreach to key HCPs within the assigned territory to build and strengthen relationships and represent the Company's interests, including those in national and regional healthcare systems, integrated delivery systems, payors, and group purchasing organizations in the areas of medical education, clinical, non-clinical and health economics and outcomes research. The Medical Science Liaison contributes to the Company's success by utilizing scientific exchange and interpersonal skills to develop relationships with healthcare practitioners (HCPs), including key opinion leaders, seeking to optimize patient outcome through proper understanding of the disease state, appropriate patient identification and appropriate utilization of the Company's product.
NewVP, Clinical Development AbSci CorpVP, Clinical DevelopmentNY$355,000–$415,000 / yearAbout the role: Reporting to the Chief Medical Officer (CMO), the Vice President, Clinical Development provides executive leadership for the companys clinical research and development activities, including Abscis proprietary biologics programs and partner-developed therapeutics leveraging our synthetic biology and AI-driven protein engineering platform. The Vice President, Clinical Development serves as a senior leader within Clinical Development, accountable for clinical trial design, execution, regulatory strategy, data integrity, and cross-functional alignment across internal programs and external partnerships.
Registered Nurse - Nursing Home Surveyor/Complaint Investigator Greenlife Healthcare StaffingRegistered Nurse - Nursing Home Surveyor/Complaint InvestigatorNew York, NYWe are seeking a dedicated and experienced Registered Nurse - Nursing Home Surveyor/Complaint Investigator to join our team in New York City, NY (Bronx, Kings, Richmond, Manhattan, and Queens). This role is a temporary-to-permanent position that involves conducting surveys, complaint investigations, and surveillance activities at nursing homes to ensure compliance with Federal and State regulations.
Director, Product Management - Examination & Analysis Magnet Forensics, Inc.Director, Product Management - Examination & AnalysisNew York, NY$190,000–$240,000 / yearThis leader will help evolve the portfolio toward more connected workflows, shared capabilities, and scalable analysis experiences while partnering closely with centralized AI leadership to apply AI in ways that meaningfully improve examiner and investigator outcomes. While the Magnet Axiom, a Magnet Flagship Product, remains a core responsibility, the scope of this role extends beyond a single product and focuses on the broader workflow, capability, and platform ecosystem supporting digital investigations.
Registered Nurse Greenlife Healthcare StaffingRegistered NurseNew York, New York$60Position Overview: We are seeking a dedicated and experienced Registered Nurse - Nursing Home Surveyor/Complaint Investigator to join our team in New York City, NY (Bronx, Kings, Richmond, Manhattan, and Queens). About Greenlife Healthcare Staffing: Greenlife Healthcare Staffing is a leading nationwide recruitment agency dedicated to connecting healthcare professionals with top-tier opportunities.
Asset Protection Investigator Saks Fifth AvenueAsset Protection InvestigatorNew York City, New York$23.58–$29.47 / hourUnder direction from the Asset Protection Manager or Assistant General Manager Operations, the Associate Asset Protection Manager is responsible for managing the Asset Protection staff, monitoring shortage results, shortage control, investigations and apprehensions regarding internal and external theft, and implementation of store safety and awareness programs at an individual Saks Fifth Avenue location. Trusted for inventive and game changing ideas to even the most complex challenges, constantly seeks improvement and new ways to do things by challenging convention.
NewResearch Associate – Oncology 5PY IQVIA RDS Inc.Research Associate – OncologyWhippany, NJ$47,400–$169,300 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
NewResearch Associate 5PY IQVIA RDS Inc.Research AssociateWhippany, NJ$47,400–$169,300 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.