Clinical Trial Associate Cellectis SAClinical Trial AssociateNew York, NY$80,000–$90,000 / yearSupport study start-up activities, including site feasibility, investigator onboarding, and collection of regulatory and essential documents • Assist with site management activities throughout the trial lifecycle, from start-up through close-out • Communicate with clinical sites and vendors, as appropriate, to support timely collection of required documentation • Support investigational product tracking activities, including inventory documentation, shipment tracking, and reconciliation. • Maintain accurate, complete, and inspection-ready Trial Master Files (electronic or paper) • Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness • Review, file, and track clinical trial documentation in accordance with SOPs and regulatory requirements • Assist with quality control (QC) checks of study, country, and site-level documentation and support issue resolution.
Senior Project Manager, Laboratory ICON PlcSenior Project Manager, LaboratoryFarmingdale, NYAct as the sponsors main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. Key responsibilities include: Ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Central Laboratories' (ICL) services, including the setup and day-to-day management of studies.
Director, Clinical Study Management Eikon Therapeutics IncDirector, Clinical Study ManagementJersey City, NJ$203,000–$221,350 / yearEikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City, New Jersey or Millbrae, California offices to ensure effective management and high-performance delivery of clinical studies.
Development Head, RSV, RSV Combination, and Early Vaccine Programs Pfizer IncDevelopment Head, RSV, RSV Combination, and Early Vaccine ProgramsPearl River, NY$330,200–$550,400 / yearApplies technical/scientific expertise to resolve issues regarding the clinical components of documents (e.g., Investigational New Drugs, New Drug Applications/Common Technical Documents, global registration dossiers, lifecycle strategy documents, internal documents). Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Deployment Strategist Valon Mortgage, Inc.Deployment StrategistNew York, NY$135,000–$240,000 / yearA track record of structured problem solving under pressure: operating roles, strategy consulting, banking, investing, Chief of Staff roles, founding experience, product or business operations, high-stakes customer work, or other environments where you had to figure things out quickly. We are especially excited by high-horsepower operators, consultants, bankers, investors, Chiefs of Staff, founders, product or business operators, and people from other intense environments who have had to solve ambiguous problems under pressure.
NewCOVID-19 Vaccines, Medical Evidence Strategy Lead - MD (Sr. Director) Pfizer IncCOVID-19 Vaccines, Medical Evidence Strategy Lead - MD (Sr. Director)New York City, NY$274,500–$457,500 / yearThe foremost priority will be in setting strategy for the generation of real-world evidence across Pfizer and in collaboration with BioNTech to ensure COVID-19 studies are conducted with scientific rigor and operational efficiency in support of regulatory requirements, public health needs and education of and interactions with healthcare providers. The individual filling this position will assume the role of the Global Medical Evidence Strategy Lead within the COVID-19 vaccine franchise and will assume primary responsibility for overseeing the strategy for COVID-19 medical evidence generation and interpretation; to include but not limited to vaccine effectiveness and COVID-19/SARS-CoV-2 burden studies.
NewCOVID-19 Vaccines, Medical Evidence Strategy Lead (Sr. Director) Pfizer IncCOVID-19 Vaccines, Medical Evidence Strategy Lead (Sr. Director)Pearl River, NY$230,900–$384,800 / yearThe foremost priority will be in setting strategy for the generation of real-world evidence across Pfizer and in collaboration with BioNTech to ensure COVID-19 studies are conducted with scientific rigor and operational efficiency in support of regulatory requirements, public health needs and education of and interactions with healthcare providers. The individual filling this position will assume the role of the Global Medical Evidence Strategy Lead within the COVID-19 vaccine franchise and will assume primary responsibility for overseeing the strategy for COVID-19 medical evidence generation and interpretation; to include but not limited to vaccine effectiveness and COVID-19/SARS-CoV-2 burden studies.
Global Development Lead, Internal Medicine (Md, Sr. Director) PfizerGlobal Development Lead, Internal Medicine (Md, Sr. Director)Pearl River, NY$274,500–$457,500 / yearResponsible for comprehensive clinical development plan to secure approval and reimbursement globally (including China and Japan) along with creating the pediatric investigation plan / pediatric study plan and associated protocol design documents working closely with individual trial clinicians to ensure trial feasibility and optimized operational execution. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Development Head, Rsv, RSV Combination, And Early Vaccine Programs PfizerDevelopment Head, Rsv, RSV Combination, And Early Vaccine ProgramsPearl River, NY$330,200–$550,400 / yearApplies technical/scientific expertise to resolve issues regarding the clinical components of documents (e.g., Investigational New Drugs, New Drug Applications/Common Technical Documents, global registration dossiers, lifecycle strategy documents, internal documents). Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Clinical Research Coordinator- Manhattan, NY (Temp to Perm) The IMA GroupClinical Research Coordinator- Manhattan, NY (Temp to Perm)New York, New York$24–$31.50 / hourOur Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
Asbestos Technician / Special Inspector TectonicAsbestos Technician / Special InspectorAstoria, New YorkACI Concrete Field Testing Technician Certification is a plus; training and certification support will be provided for qualified candidates; OSHA safety training preferred; ability to obtain required certifications upon employment; Strong attention to detail and ability to accurately document field observations and project findings; Excellent written, verbal, and interpersonal communication skills; Strong organizational skills and ability to manage multiple assignments; Proficiency with Microsoft Outlook, Word, Excel, and PDF software; Ability and willingness to travel regularly to project sites throughout the NYC metropolitan area, including occasional work outside normal business hours; Valid driver's license and personal vehicle required. High School Diploma or equivalent required; Minimum 2 years of asbestos inspection, air monitoring, project monitoring, construction inspection, materials testing, or related experience preferred; One or more of the following certifications strongly preferred: NYS Asbestos Inspector.
GCP Sr. Auditor Paramus, NJ unitedmstates ESRhealthcare and EXEC STAFF RECRUITERSGCP Sr. Auditor Paramus, NJ unitedmstatesParamus, New JerseyExperience level: Mid-senior Experience required: 5 Years Education level: Bachelors degree Job function: Accounting/Auditing Industry: Pharmaceuticals Pay rate: View hourly payrate Total position: 1 Relocation assistance: No Visa sponsorship eligibility: No. This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and Manufacturing to manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
CMC Writer CMC Writer Paramus, NJ $$$ bonus ESRhealthcare and EXEC STAFF RECRUITERSCMC Writer CMC Writer Paramus, NJ $$$ bonusParamus, New JerseyA Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) Writer plays a crucial role in regulatory submissions by preparing technical documents related to drug development, manufacturing, and quality control. Experience level: Mid-senior Education level: Bachelors degree Job function: Health Care Provider Industry: Pharmaceuticals Pay rate: Total position: 1 Relocation assistance: No Visa sponsorship eligibility: No.
NewCovid-19 Vaccines, Medical Evidence Strategy Lead - MD (Sr. Director) PfizerCovid-19 Vaccines, Medical Evidence Strategy Lead - MD (Sr. Director)Pearl River, NY$254,100–$423,500 / yearThe foremost priority will be in setting strategy for the generation of real-world evidence across Pfizer and in collaboration with BioNTech to ensure COVID-19 studies are conducted with scientific rigor and operational efficiency in support of regulatory requirements, public health needs and education of and interactions with healthcare providers. The individual filling this position will assume the role of the Global Medical Evidence Strategy Lead within the COVID-19 vaccine franchise and will assume primary responsibility for overseeing the strategy for COVID-19 medical evidence generation and interpretation; to include but not limited to vaccine effectiveness and COVID-19/SARS-CoV-2 burden studies.
Medical Science Liaison, Transplant / Infectious Diseases - Great Plains region (location in MN, MO, NE, IA, UT) Bionique Testing Laboratories LLCMedical Science Liaison, Transplant / Infectious Diseases - Great Plains region (location in MN, MO, NE, IA, UT)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.
NewMedical Science Liaison, Nephrology - North Central U.S. (location in IL, MN, WI, MI, IN) Veloxis Pharmaceuticals, IncMedical 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.
NewMedical Science Liaison, Nephrology - North Central U.S. (location in IL, MN, WI, MI, IN) Bionique Testing Laboratories 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.
NewMedical Science Liaison, Nephrology - Western United States (CA, NV, HI) Bionique Testing Laboratories LLCMedical Science Liaison, Nephrology - Western United States (CA, NV, HI)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.
Research Teaching Specialist III (Research Tech Developing Infectious Disease Diagnostics) Rutgers The State University of New JerseyResearch Teaching Specialist III (Research Tech Developing Infectious Disease Diagnostics)Newark, NJAligned with Rutgers University-New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and five centers and institutes that focus on cancer treatment and research, neuroscience, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research. Candidate must successfully complete a security risk assessment by the U.S. Department of Justice, and will be enrolled in the personnel reliability program, and be approved for access to select biological agents and toxins by the Centers for Disease Control and Prevention (CDC)/Department of Health and Human Services (DHHS) as a condition of employment.
Medical Science Liaison, Cardiovascular - Milvexian (New York City, Long Island NY) Bristol Myers SquibbMedical Science Liaison, Cardiovascular - Milvexian (New York City, Long Island NY)New York City, NYRemote$166,090–$201,262 / yearThe purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate usethrough peer to peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.