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.
Consultant - Commercial Solutions & Insights Hub (CSIH) Analytics IQVIA Holdings IncConsultant - Commercial Solutions & Insights Hub (CSIH) AnalyticsParsippany, NJ$71,200–$239,200 / yearProvide business consulting and project management: You will apply consulting methodologies to deliver engagements, create presentations for clients, manage projects, cultivate professional relationships with client teams, and work with management to prioritize needs. Analytic Services leverages the power of healthcare data to help its clients formulate methodologies that answer business questions in a broad spectrum of areas of expertise-providing deep insights into patient, payer, and prescriber behaviors.
Associate - Equity Research, SMid/ Large Cap Biotech Bank of America CorpAssociate - Equity Research, SMid/ Large Cap BiotechNew York, NY$110,000–$175,000 / yearHe or she will work alongside the Senior Analyst and Associates in all aspects of the research process, from idea generation to modeling, including but not limited to the following:Write industry and company reports and company launch initiationsDevelop doctor/patient surveys and conduct doctor interviews to understand market dynamics, demand and future projectionBuild financial models to quantitatively analyze company valuationsDemonstrate industry knowledge (such as regulatory, pricing) from early-stage study to market approvalBuild relationships and facilitate information flow with contacts at covered companiesSeek out new, value-added and/or unusual sources of informationHave ability to monitor news flow and highlight stock-impacting updates when the Senior Analyst is travelingInteract regularly with sales, trading and external clients and if performance on team is strong enough, take on coverage of individual names over time This position has a requirement of being in the office 4 days per week. Qualifications:Bachelor's Degree or equivalent years of experience (Advanced degree in life science discipline is a plus)Ideal candidate would have 1-4 years of experience in biotech equity research, buy side experience or investment banking experienceStrong writing and financial modeling skills is a mustMust enjoy following the stock market and doing desktop and field researchAcademic background in a life science field and should understand economics, macroeconomic factors and policyMust have excellent communications skills, written and verbalMust have strong attention to detail, ability to multi-taskMust work well in a collaborative team environmentMust have strong desire to be a team player and view team's success as a reflection of individual successShift:1st shift (United States of America)Hours Per Week: 40 Learn more about this role Apply × To proceed with your application, you must be at least 18 years of age.
Lead, Health Security World Economic Forum SwitzerlandLead, Health SecurityNew York, NY$120,000–$140,000 / yearThe CHH community brings together leaders from the world's top healthcare providers, insurers, biopharma, MedTech and relevant sectors to engage in key global issues with other stakeholders, including government leaders, CEOs and senior executives from adjacent industries, heads of international organizations, academics, experts, thought leaders and representatives from civil society. This position will report to the Head, Resilient Healthcare, Centre for Health and Healthcare and will work closely with colleagues and a broad range of stakeholders including private companies in healthcare and other industries, governments, international organizations, civil society organizations, research institutions, academia, and expert communities.
Radiopharmaceutical Therapy Specialist (RPTS) - US Northeast Territory ITM Isotope Technologies Munich SERadiopharmaceutical Therapy Specialist (RPTS) - US Northeast TerritoryNY$170,000–$200,000 / yearAbout ITM ITM is a privately owned biotechnology and radiopharmaceutical group of companies dedicated to the development, production and global supply of targeted diagnostic and therapeutic radiopharmaceuticals and radioisotopes for use in cancer treatment. This role serves as a key clinical resource for supporting healthcare providers, nuclear medicine departments, and radiation and medical oncology teams with ITM product portfolio adoption, implementation, and clinical integration.
Clinical Monitoring Associate Axsome Therapeutics IncClinical Monitoring AssociateNew York, NY$70,000–$80,000 / yearOur industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. May assist in the development/revision and/or provide input in the development of clinical trial related documents including but not limited to study tools, monitoring tools, presentations, meeting materials, case report forms, informed consents, timelines, clinical monitoring plans, site reference manuals, pharmacy manuals, laboratory manuals, protocols, and training materials.
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 Manager, Biostatistics Axsome Therapeutics IncSenior Manager, BiostatisticsNew York, NY$140,000–$170,000 / yearOur industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, agitation associated with dementia due to Alzheimer's disease, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, as well as multiple novel product candidates addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Reporting to the Senior Director, Biostatistics, the Senior Manager, Biostatistics will serve as lead statistician on assigned clinical trials, and in collaboration with project team members provide statistical input on trial design, protocol development, and manage creation of Statistical Analysis Plans (SAPs).
Director, Global Berobenatide Launch & Commercial Development PfizerDirector, Global Berobenatide Launch & Commercial DevelopmentNew York City, New York$176,600–$294,300 / yearOperating as a leader within a highly dynamic and evolving therapeutic area, this role requires a strong sense of urgency, the ability to navigate significant ambiguity, and the capacity to seamlessly shift between detailed asset-level execution and broader strategic direction. 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.
New["Sales Leadership Insights & Execution Director","Sales Leadership Insights & Execution Director"] Pfizer["Sales Leadership Insights & Execution Director","Sales Leadership Insights & Execution Director"]New York$176,600–$294,300 / yearLeveraging the sales data and analysis made available by the Enablement function, it generates macro and micro‑level analysis that gives the Sales Lead, Regional Business Directors (RBDs), and Area Business Managers (ABMs) clear, fast, actionable direction, ready‑to‑use coachable insights, and strategic execution. Driving Decision Velocity Compress the cycle from “we have a number to hit” to “here is where to invest leadership attention” by turning provided sales data into analysis that defines positive and negative trends, identifies opportunities, risks, gaps and successes, as well as supports top‑down deployment, bottom‑up escalation, and collaborative planning.
Executive Director, Global Project Leader Shionogi Inc.Executive Director, Global Project LeaderFlorham Park, New Jersey$285,000–$315,000 / yearOverview: The Global Project Leader provides strategic and operational leadership for one or more global clinical development programs within a complex, global rare disease portfolio, spanning early development through registration and lifecycle management. 12+ years of experience in pharmaceutical/biotechnology development with demonstrated leadership in global, cross-functional settings; experience in rare disease development strongly preferred.
Director, Global Epidemiology & Real-World Evidence Shionogi Inc.Director, Global Epidemiology & Real-World EvidenceFlorham Park, New Jersey$230,000–$265,000 / yearThis role provides scientific and methodological leadership for observational research and evidence generation, partners cross-functionally to integrate RWE into development and medical strategies, and oversees key vendor relationships and external collaborations. Overview: The Director, Global Epidemiology & Real-World Evidence leads epidemiology and RWE activities across assigned therapeutic areas, with a strong focus on the U.S., in alignment with global strategy.
Director, Corporate Communications Melinta Therapeutics LLCDirector, Corporate CommunicationsParsippany, NJThe Director serves as a trusted advisor to senior leadership, translating complex scientific and business information into clear, compliant messaging for diverse internal stakeholders and partnering cross-functionally to ensure communications align with organizational objectives and values. We are seeking a strategic and collaborative Director, Corporate Communications to lead integrated internal and external, excluding investor relations, communications that strengthen corporate reputation, support business priorities, enhance company culture through employee engagement, and advance our scientific mission.
Sr Project Manager LancesoftSr Project ManagerFranklin Lakes, NJ$90The candidate will work under the guidance of a Senior Director, and must be capable of working independently to drive and orchestrate cross functional activities. The candidate will work under the guidance of a Senior Director, and must be capable of working independently to drive and orchestrate cross functional activities .
Clinical Trial Manager 4D Molecular Therapeutics IncClinical Trial ManagerNY$150,000–$170,000 / yearAssist in preparation and review of clinical trial documentation such as; protocol, informed consent, Investigator Brochure, Clinical Monitoring Plan, Project Plan, Case Report Forms, Statistical Analysis Plan, Clinical Study Reports, and other study level documents. MAJOR DUTIES & RESPONSIBILITIES: Trial Management: Serve as the primary unmasked contact for managing protocol execution, including oversight of the unmasked CRO, other study service providers, and consultants that are involved in a clinical trial.
Associate Director, Biostatistics 4D Molecular Therapeutics IncAssociate Director, BiostatisticsNY$193,000–$212,000 / yearThe Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients.
Device Support Specialist - Northern NJ / Hudson Valley, NY NovoCure LtdDevice Support Specialist - Northern NJ / Hudson Valley, NYNew Jersey, NJ$64,000–$66,000 / yearThe DSS focuses on educating patients and their caregivers on TTFields according to product labeling and integrating TTFields into daily routines in order to reach usage goals. Travel to patient homes, and occasionally to physician offices or healthcare centers, to conduct regular visits which include: Educate patients on TTFields therapy and initiating treatment.
Director, Global Epidemiology & Real World Evidence Shionogi & Co LtdDirector, Global Epidemiology & Real World EvidenceFlorham Park, NJ$230,000–$265,000 / yearThis role provides scientific and methodological leadership for observational research and evidence generation, partners cross-functionally to integrate RWE into development and medical strategies, and oversees key vendor relationships and external collaborations. The Director, Global Epidemiology & Real-World Evidence leads epidemiology and RWE activities across assigned therapeutic areas, with a strong focus on the U.S., in alignment with global strategy.
Product Management and Marketing Talent - Join our Commercial Talent Community! GenScript/ProBioProduct Management and Marketing Talent - Join our Commercial Talent Community!Piscataway, NJGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products.
Director, IVD Regulatory Consulting Precision Medicine Group LLCDirector, IVD Regulatory ConsultingNY$162,000–$243,000 / yearPosition Summary: The Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing authorization pathways to advise pharmaceutical, biotechnology, and diagnostic clients on the development, clinical trial use, approval, and lifecycle management of companion diagnostics. Direct the preparation of global regulatory submissions and supporting documentation for companion diagnostics and clinical trial assays, including FDA Q-Submissions, Pre-IDE packages, IDEs, PMAs, PMA supplements, EU IVDR Annex XIV performance study applications, technical documentation, and other country-specific submissions.