NewAssociate Director, Clinical Operations PTC TherapeuticsAssociate Director, Clinical OperationsWarren, NJ$170,200–$214,200 / yearPrimary duties/responsibilities: Performs as an integrated member of the clinical team to lead, direct and contribute to, the planning, execution, and reporting of clinical trials, including estimation of clinical project timelines, protocol writing, Case Report Form (CRF) design, site selection, study drug forecasting, site and Clinical Research Organization (CRO) management, data review, and study reporting; recommends monitoring, safety, eligibility, enrollment, and data consistency strategies. Manages clinical study timelines using the appropriate project management tools; develops budgets and manages expenditures for clinical trial program, including those for investigational sites and vendors; presents project progress reports through accurate, succinct summaries of clinical study work at internal team meetings and investigator meetings.
Contract, Clinical Operations PTC Therapeutics IncContract, Clinical OperationsWarren, NJ$60–$80 / hourPrimary duties/responsibilities: Performs as an integrated member of the clinical team to lead, direct and contribute to, the planning, execution, and reporting of clinical trials, including estimation of clinical project timelines, protocol writing, Case Report Form (CRF) design, site selection, study drug forecasting, site and Clinical Research Organization (CRO) management, data review, and study reporting; recommends monitoring, safety, eligibility, enrollment, and data consistency strategies. Manages clinical study timelines using the appropriate project management tools; develops budgets and manages expenditures for clinical trial program, including those for investigational sites and vendors; presents project progress reports through accurate, succinct summaries of clinical study work at internal team meetings and investigator meetings.
Project Manager Medidata Solutions IncProject ManagerNew York, NY$96,000–$128,000 / yearCelebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster.
2027 Future Talent Program - QA Research Clinical Quality, Analytics & AI - Co-Op Merck & Co Inc2027 Future Talent Program - QA Research Clinical Quality, Analytics & AI - Co-OpRahway, NJThe team collaborates with business and Digital/IT partners to build dashboards, applications, analytics capabilities, and AI-enabled solutions while advancing awareness and education around analytics, data science, and emerging technologies. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
NewSenior Clinical Science Specialist, Rare Disease / Liver, North Florida Ipsen SASenior Clinical Science Specialist, Rare Disease / Liver, North FloridaBerkeley Heights, NJ$135,000–$198,000 / yearManage the assigned geography and customer accounts in an efficient manner, following principles of key physician/account prioritization, daily call reporting, and resource utilization. Knowledge & Experience: Eight years life-sciences experience, including at least five years in rare or specialty areas, and at least three years in specialty biopharma sales.
Senior Clinical Science Specialist, Rare Disease / Liver, Providence RI and Eastern CT Ipsen SASenior Clinical Science Specialist, Rare Disease / Liver, Providence RI and Eastern CTBerkeley Heights, NJ$135,000–$195,000 / yearManage the assigned geography and customer accounts in an efficient manner, following principles of key physician/account prioritization, daily call reporting, and resource utilization. This role manages complex accounts, engages diverse stakeholders, and leverages data to drive strategic decisions and outcomes.
Supervisor, Clinical Therapists - Full Time - Behavioral Health Hackensack Meridian HealthSupervisor, Clinical Therapists - Full Time - Behavioral HealthBelle Mead, New JerseyFull timeThe posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package. Responsibilities: A day in the life of a Supervisor, Clinical Therapists at Hackensack Meridian Health includes: Facilitates collaborative management of patient care across the continuum, intervening as necessary to remove barriers to timely and efficient care delivery and reimbursement.
Clinical Care Coordinator RN - Home Care- Iselin, NJ- FT Hackensack Meridian HealthClinical Care Coordinator RN - Home Care- Iselin, NJ- FTIselin, New JerseyFull timeApplies clinical knowledge and skills (i.e., administration of medications, treatments, procedures, etc.) to safely provide direct patient care in a professional, caring, culturally- sensitive, and cost efficient manner; ensuring appropriate clinical coordination and support of patients and families. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Clinical Care Coordinator RN VHS-Homecare-Woodland Park, NJ-FT Hackensack Meridian HealthClinical Care Coordinator RN VHS-Homecare-Woodland Park, NJ-FTWoodland Park, New JerseyFull timeApplies clinical knowledge and skills (i.e., administration of medications, treatments, procedures, etc.) to safely provide direct patient care in a professional, caring, culturally- sensitive, and cost efficient manner; ensuring appropriate clinical coordination and support of patients and families. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Clinical Speciality Programs & Operations Manager - NY Atria Health and Research InstituteClinical Speciality Programs & Operations Manager - NYNew York, NY$100,000–$120,000 / yearAfter successfully opening our flagship Institute in New York in 2022 and expanding to South Florida in 2024, we are now bringing the Atria experience to the West Coast with the launch of our Los Angeles Institute in late spring 2026.?. The position sits at the intersection of clinical operations, care delivery, finance, technology, and growth strategy, ensuring Atria can expand specialty programs and new markets while maintaining a high-touch member experience and operational excellence.
BMT Clinical Account Manager Omeros CorpBMT Clinical Account ManagerNY$215,000–$240,000 / yearOmeros' lead complement inhibitor YARTEMLEA (narsoplimab-wuug), which targets the lectin pathway's effector enzyme MASP-2, is FDA-approved and commercially available in the U.S. for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA) in adult and pediatric patients aged two years and older. Omeros' pipeline also includes OMS527, a phosphodiesterase 7 inhibitor in clinical development for cocaine use disorder, which is fully funded by the National Institute on Drug Abuse, and a growing portfolio of novel recombinant antibodies targeting multidrug-resistant organisms and novel molecular and cellular therapeutic programs for oncology.
Senior Manager, Clinical Data Systems AbbVie, IncSenior Manager, Clinical Data SystemsFlorham Park, NJApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
Senior Director Clinical Development, Breast Cancer BeOne Medicines AGSenior Director Clinical Development, Breast CancerNY$299,800–$369,800 / yearThe Senior Director, Clinical Development, Solid Tumors will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical scientist role.
Senior Director, Clinical Development PTC Therapeutics IncSenior Director, Clinical DevelopmentWarren, NJ$289,200–$364,000 / yearFacilitates communication and collaboration with internal, cross-functional team members including, but not limited to, research, manufacturing, drug supply, regulatory, quality assurance, marketing and external key stakeholders including, but not limited to, collaborators, KOLs, investigators and domestic and international regulatory authorities, to support CDPs, regulatory submissions and clinical development goals. Clinical Research Organizations (CROs) and other vendors, consultants, collaborators, etc.); monitors program/study budgets to ensure the timely and cost-effective implementation of CDP(s); reviews and approves contracts, work orders and invoices within grant of authority; participates in the assessment of CROs, vendors, consultants or other partners as necessary.
Sourcing Specialist-Clinical NYU Langone Medical CenterSourcing Specialist-ClinicalNew York, NY$84,577.92–$110,000 / yearMinimum of two to three years Supply Chain experience, and preferably one (1) year in strategic sourcing responsibilities for various commodities, both products and services within and outside healthcare organizations. NYU Langone Health is a fully integrated health system that consistently achieves the best patient outcomes through a rigorous focus on quality that has resulted in some of the lowest mortality rates in the nation.
Contract Manager Revolution Medicines IncContract ManagerNYRemote$129,000–$160,000 / yearManage the end-to-end lifecycle for a high volume of agreements across the company's commercial and clinical/research functions, including master services agreements, consulting and vendor agreements, amendments, change orders, clinical trial-related agreements, research collaborations, and other commercial, operational, or life-sciences contracts, in accordance with company policies and applicable regulatory, privacy, and compliance requirements. Reporting to the Associate Director, Contract Management, this role will support contracts across the entire company, spanning the full spectrum of commercial activities-including marketing, sales, corporate and vendor matters, procurement, and IT-as well as clinical and research activities, including clinical trial-related, research collaboration, and other life-sciences agreements.
Clinical Data Manager (STEM-Focused) System OneClinical Data Manager (STEM-Focused)New York, New York$50–$60 / hourThis role is ideal for someone who can operate as a true partner to cross-functional teams, bringing both technical expertise and scientific insight to clinical data management activities. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
Executive Director, Geo Lead & Global Capability Lead, Clinical Data Management Services (US) Merck & Co IncExecutive Director, Geo Lead & Global Capability Lead, Clinical Data Management Services (US)Rahway, NJ$231,900–$365,000 / yearNetworking & Partnerships | Proactively builds and sustains strategic internal and external relationships (cross-functional leaders, service providers, alliance partners, customers) to accelerate functional area and geography-specific objectives. Jointly accountable with Portfolio & Resource Operations and non-GDMS leaders for planning, resourcing, and operational governance across regions; set priorities for resource allocation, capability development, and continuous improvement or process innovation to achieve strategic and operational goals.
Manager of Orthopedic Lab Research Maimonides Medical CenterManager of Orthopedic Lab ResearchBrooklyn, New York$56,000–$66,000 / yearFull timeThe system is anchored by Maimonides Medical Center, one of the nation’s largest independent teaching hospitals and home to centers of excellence in numerous specialties; Maimonides Midwood Community Hospital (formerly New York Community Hospital), a 130-bed adult medical-surgical hospital; and Maimonides Children's Hospital, Brooklyn's only children's hospital and only pediatric trauma center. We uphold and maintain Honesty, Empathy, Accountability, Respect, and Teamwork to empower our talented team, engage our respective communities and adhere to Planetree's philosophy of patient-centered care.
Senior Proposal Manager Clinilabs IncSenior Proposal ManagerNY$115,000–$125,000 / yearThis role manages the proposal process from initial RFP intake through final submission, working cross-functionally with Business Development, Operations, Finance, Legal, Contracts, and other subject matter experts to ensure proposals are accurate, competitive, compliant, and aligned with sponsor requirements. Ability to review and interpret protocols/SOAs, RFP materials, sponsor requirements, bid grids, assumptions, scopes of work, vendor inputs, and operational feedback to support accurate pricing, comprehensive budget development, risk identification, proposal strategy, and alignment with clinical trial operational requirements.