Case Investigator, Bureau of Communicable Diseases City of New YorkCase Investigator, Bureau of Communicable DiseasesQueens, NYAs the primary population health strategist and policy authority for NYC, with a rich history of public health initiatives and scientific advancements, from addressing the 1822 yellow fever outbreak to the COVID-19 pandemic, we serve as a global leader in public health innovation and expertise. Reporting to the Disease Investigation Unit's Team Lead and working with a team of Public Health Epidemiologists, City Research Scientists and Clerical Associates, you will investigate cases of reportable diseases and outbreaks of infectious or novel conditions.
Case Investigator City of New YorkCase InvestigatorNew York, NYKnowledge of communicable disease surveillance and epidemiologic investigations - Experience with structured interviews, medical terminology and conducting electronic health record reviews - Comfortable discussing sensitive topics including sexual activity and drug use - Experience working with healthcare providers - Strong organizational and time management skills - Proficient with word processing, spreadsheet, and presentation software. Position Summary: Reporting to the Disease Investigation Unit's Team Lead and working with a team of Public Health Epidemiologists, City Research Scientists and Clerical Associates, you will investigate cases of reportable diseases and outbreaks of infectious or novel conditions.
Clinical Investigator Oscar Health IncClinical InvestigatorNew York, NYRemote$75,348–$98,894 / yearBonus points: Bachelor of Science in Nursing (BSN), Associate Degree in Nursing (ADN) with a Bachelor of Science in Health Administration, Clinical Informatics, or a related Medical Science field, or Associate Degree in Nursing (ADN) with 5+ years of specialized clinical audit experience. Work Location: This is a remote position, open to candidates who reside in: Arizona, Florida, Georgia, Illinois, Iowa, Kansas, Michigan, Missouri, Nebraska, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas and Virginia.
2027 Future Talent Program - Clinical and Regulatory Strategic Communications - Intern Merck & Co Inc2027 Future Talent Program - Clinical and Regulatory Strategic Communications - InternRahway, NJ$39,908–$111,111 / yearClinical Regulatory & Strategic Communications (CRSC) is a multidisciplinary organization that plays a critical role in supporting the development of new medicines by creating key clinical and regulatory documents, communicating clinical trial results, and ensuring information is shared responsibly and transparently with regulatory agencies, healthcare professionals, trial participants, and the public. Seeking a highly motivated individual who is pursuing an education in the life sciences, medicine, pharmacology/pharmacy, quality, operations, data science, or a related field, and who is interested in writing, communicating about medicine and science, and supporting the quality, compliance and operational excellence activities that enable clinical research.
Sr. Clinical Trial Manager, Therapeutics and Oncology Moderna IncSr. Clinical Trial Manager, Therapeutics and OncologyPrinceton, NJ$130,800–$209,400 / yearWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate.
US Senior Medical Director, Rare Hematology SanofiUS Senior Medical Director, Rare HematologyMorristown, NJ$206,250–$343,750 / yearThe mission of this team is to support the company by functioning as the internal expert in rare hematologic conditions - focusing on recent launch in Immune Thrombocytopenia (ITP), and potentially including warm Autoimmune Hemolytic Anemia (wAIHA), and Sickle Cell Disease (SCD) among other rare blood disorders - and helping Health Care Professionals and Payers optimize patient care and treatment outcomes through evidence-based decisions. The Senior Medical Director will establish and maintain collaborative medical and scientific relationships with key external physicians and internal constituencies from multiple functional groups - including, but not limited to, Medical Affairs, Clinical Research, Regulatory, Science, Marketing, Sales, Commercial Operations, and Patient and Product Services - while maintaining full compliance with all relevant company, industry, legal, and regulatory requirements.
US Senior Medical Director Neurology SanofiUS Senior Medical Director NeurologyMorristown, NJ$206,250–$297,916.66 / yearMain Responsibilities: Provide strategic leadership to the US Medical Affairs Next Gen Immunology team (Medical Directors, Medical Science Liaison Managers, and Medical Science Liaisons) by cultivating a culture of teamwork and collaboration to ensure the delivery of key priorities while attracting, developing, and retaining top talent. Develop strategy and tactics for an integrated Medical Plan encompassing Medical Science Liaisons, Medical Education, Medical Communications and Publications, Health Outcomes, Safety, and Clinical Research (Phase IIIB-IV and Investigator Sponsored Trials) across the neurology pipeline.
Medical Operations Manager - NA PhotocureMedical Operations Manager - NAPrinceton, NJRemote$180,000–$210,000 / yearThis hybrid role includes operational oversite of projects in clinical development as well as post-approval studies at Photocure, in particular, the U.S. Cysview Blue Light Cystoscopy Registry, a large multi-center study collecting Real-World Evidence (RWE) from bladder cancer patients undergoing treatment. Specific Responsibilities and Activities include: Act as the primary point of contact for operational stewardship and oversight of the research projects including sponsored studies, the U.S. Cysview Registry and IITs (Investigator Initiated Trials).
Scientific Director, Breast Cancer Portfolio Artera IncScientific Director, Breast Cancer PortfolioNY$145,000–$165,000 / yearThe Scientific Director, Breast Cancer Portfolio, within the Clinical Development department, will provide scientific and strategic leadership for evidence generation across a portfolio of breast cancer diagnostic products spanning early development, clinical validation, regulatory submission, and post-market management. Serve as the scientific lead for the breast cancer evidence portfolio by maintaining continuity across studies, coordinating scientific priorities across collaborators and internal stakeholders, and ensuring that research activities remain aligned with long-term portfolio objectives.
Senior Medical Director/Medical Director, Clinical Trial Lead KardiganSenior Medical Director/Medical Director, Clinical Trial LeadPrinceton, New Jersey$242,000–$347,000 / yearThe Senior Director / Medical Director - Clinical Trial Lead will be a physician with extensive drug development expertise who will be expected to lead to the clinical development strategy for the phase 1-3 clinical trials of the program, including the protocol design, operational planning and trial execution, medical and safety monitoring, trial close out, trial results interpretation, and preparation for dissemination of the trial results, working with academic partners. Takes primary responsibility for the clinical development function, working with statisticians, modelers, and project team-members, for contributing to the creation of trial-specific statistical analysis plans, and for the interpretation, reporting, and dissemination of the final results, working closely with academic partners.
Senior Manager, Financial Reporting & Technical Accounting FalconXSenior Manager, Financial Reporting & Technical AccountingNew York City, NY; Remote; San Francisco Bay Area$157,000–$199,000 / yearOperating at the intersection of traditional finance and cutting-edge technology, FalconX addresses the industry's foremost challenges: Navigating the digital asset market can be complex and fragmented, with limited products and services that support trading strategies, structures, and liquidity found in conventional financial markets. Background: Proven track record transitioning from Big 4 Audit/Technical Desks into Accounting Advisory (e.g., CFGI, FTI, EY, KPMG) or In-House Accounting leadership at a high-growth digital assets firm, FinTech startup, broker-dealer, or Investment Bank.
Special Agent U.S. Department of Homeland SecuritySpecial AgentQueens, NY$48,854–$118,204 / yearYou are minimally qualified for the GL-07 Level starting base salary 48854 if you possess one of the following: A bachelors degree from an accredited college or university with Superior Academic Achievement (S.A.A.), which is based on: Class standing: Applicants must be in the upper third of the graduating class in the college, university, or major subdivision (such as the College of Liberal Arts or the School of Business Administration) based on completed courses. Grade-point average (G.P.A.): Applicants must have a grade-point average of 3.0 or higher out of a possible 4.0 (B or better) as recorded on their official transcript or as computed based on 4 years of education or as computed based on courses completed during the final 2 years of the curriculum.
Director, Field Translational Science - Oncology Natera IncDirector, Field Translational Science - OncologyNY$150,000–$220,000 / yearThis high-autonomy leadership role is designed for a strategic builder who can run a sophisticated regional team while serving as the executive authority for advanced Natera tests - including, but not limited to, cell-free DNA (cfDNA) and minimal residual disease (MRD) assays - and their associated data analysis frameworks across elite academic medical centers. Investigator-Led Portfolio Management: In partnership with MSLs, oversee the lifecycle of all regional investigator-initiated trials (IITs) and institutional registries, ensuring team members enable investigators to maximize the utility of Natera's proprietary analytical tools and data visualization platforms to achieve statistical robustness and prompt manuscript generation.
Senior Trainer, Clinical Education Care Access Research LLCSenior Trainer, Clinical EducationNYRemote$100,000–$130,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Drive the development, review, and maintenance of documentation, training templates, study-specific training, and platform-specific user guides tailored to Care Access tools (e.g., ST, UPVIO, CRIO, IT Support and Supply Portal, Fusion Live, Safety Culture) and/or sponsor provider platforms.
Clearance Supervisor, Bureau of Childcare City of New YorkClearance Supervisor, Bureau of ChildcareManhattan, NYDUTIES WILL INCLUDE BUT NOT BE LIMITED TO: Provide citywide education, outreach, referral and technical assistance to operators and staff of child care centers, home-based child care programs, after school programs and summer camps regarding background clearances necessary to attain, renew or maintain a license to provide services that are necessary to protect the health and safety of children while in the child care environment. A four-year high school diploma or its educational equivalent and five years of satisfactory, full-time experience as an investigator evaluating credit worthiness, searching for assets, verifying information concerning education, experience, and other personal qualifications bearing upon character and fitness for employment, or performing investigations involving the research, compilation and/or location of evidence or information in order to build a case or uncover activities of a criminal, corrupt, unlawful or unethical nature; or.
Clearance Administrator, Bureau of Childcare City of New YorkClearance Administrator, Bureau of ChildcareMANHATTAN, NYA four-year high school diploma or its educational equivalent and two years of satisfactory, full-time experience as an investigator evaluating credit worthiness, searching for assets, verifying information concerning education, experience, and other personal qualifications bearing upon character and fitness for employment; or performing investigations involving the research, compilation and/or location of evidence or information in order to build a case or uncover activities of a criminal, corrupt, unlawful or unethical nature; or. The Bureau routinely monitors child care programs to protect the health and safety of children while in the child care environment and actively works to improve and expand access to high quality programs which support early childhood development and learning.
Clearance Administrator City of New YorkClearance AdministratorNew York, NYA four-year high school diploma or its educational equivalent and two years of satisfactory, full-time experience as an investigator evaluating credit worthiness, searching for assets, verifying information concerning education, experience, and other personal qualifications bearing upon character and fitness for employment; or performing investigations involving the research, compilation and/or location of evidence or information in order to build a case or uncover activities of a criminal, corrupt, unlawful or unethical nature; or. With a staff of 1,000, the Division covers a broad range of subject matter, including oversight of environmental investigations, lead poisoning, injury prevention, occupational health, food safety, childcare, radiation control, recreational and drinking water quality, air quality, climate health, vector control, veterinary public health and pest control.
Distinguished Scientist, Safety Assessment Project Expert SanofiDistinguished Scientist, Safety Assessment Project ExpertMorristown, NJ$178,500–$257,833.33 / yearThese activities entail formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies, authoring regulatory documents, being a member of an integrated Project Team, interacting with internal and external partners, and interacting with and responding to global regulatory agencies. Our Team: The candidate will be part of a dynamic interactive Preclinical Safety group that spans all aspects of the drug development value chain providing toxicology and safety pharmacology expertise as a member of global project teams.
Clinical Research Director SanofiClinical Research DirectorMorristown, NJ$206,250–$343,750 / yearParticipates and contributes to regulatory and safety documents and discussions: Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
Medical Science Liaison - Southeast Region (FL, GA, AL, TN, MS, PR) ImCheck Therapeutics SASMedical Science Liaison - Southeast Region (FL, GA, AL, TN, MS, PR)Berkeley Heights, NJ$185,000–$215,000 / yearResponsibilities will include, but are not limited to the following: Identify, gain access to, and develop peer to peer relationships with regional and national thought leaders, active and potential study investigators, providers at academic and non-academic institutions and professional organizations within assigned geography. This role is responsible for engaging with national and regional Thought Leaders (TLs), Investigators, and Healthcare Providers (HCPs) to exchange scientific insights, support clinical research, and facilitate both clinical trial efforts and Investigator-Sponsored Studies (ISS).