Associate Director, Outcomes Research Merck & Co IncAssociate Director, Outcomes ResearchRahway, NJ$156,900–$247,000 / yearUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
NewClinical Data Manager SystImmune, Inc.Clinical Data ManagerPrinceton, NJ$100,000–$170,000 / yearIndependently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data review, and support company deliverables.
2027 Future Talent Program -Global Clinical Trial Operations (GCTO) Project Management Office (PMO) - Intern PMO Intern Merck & Co Inc2027 Future Talent Program -Global Clinical Trial Operations (GCTO) Project Management Office (PMO) - Intern PMO InternRahway, NJ$39,908–$111,111 / yearThe intern will engage with the Project Management Office (PMO) organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of clinical trials across GCTO. Required Education and Skills: Candidates must be currently enrolled in a full-time BS/BA degree program in a business or project management, continuous improvement, computer technology, or science related discipline.
NewAssociate Director, Clinical Operations PTC Therapeutics IncAssociate 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.
Student Assistant (Research) Rutgers The State University of New JerseyStudent Assistant (Research)Newark, NJAligned with Rutgers University-New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and six centers and institutes that focus on cancer treatment and research, neuroscience, clinical and translational research, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research. The Student Assistant will assist the Associate Dean with research projects addressing the mechanisms through which historically and contemporary under resourced populations experience health inequities; engaging in theoretically driven research that seeks to disentangle the effects of different social determinants of health on the outcomes of these populations.
2027 Future Talent Program - Global Clinical Trial Operations Epidemiology Operations - Intern Merck & Co Inc2027 Future Talent Program - Global Clinical Trial Operations Epidemiology Operations - InternRahway, NJ$39,908–$111,111 / yearThe intern will engage with the Epidemiology Operations organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of epidemiology trials across GCTO. Required Education: Candidates must be currently enrolled in a full-time BS/BA (or higher) degree program in a business or project management, continuous improvement, computer technology, or science related discipline.
Senior Director, Clinical Development Metabolism (MASH) Merck & Co IncSenior Director, Clinical Development Metabolism (MASH)Rahway, NJ$282,200–$444,200 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with a particular focus on MASH (Metabolic Dysfunction-Associated Steatohepatitis) and other obesity-related disorders.
NewPrincipal Scientist, Translational Clinical Biomarkers - Hematology/Oncology Merck & Co IncPrincipal Scientist, Translational Clinical Biomarkers - Hematology/OncologyRahway, NJ$190,800–$300,300 / yearRequired Skills: Biomarkers, Clinical Development, Clinical Research, Ethical Compliance, Immuno-Oncology, Mechanism of Action, Oncology, Patient Care, Pharmacodynamics, Protocol Development, Research Designs, Scientific Presentations, Scientific Writing, Strategic Thinking, Translational Medicine. For solid tumors, develop strategies addressing target expression, tumor biology, molecular subtype, immune contexture, circulating biomarkers, mechanisms of response and resistance, and potential predictive biomarkers.
Temporary Research Assistant (Junior Data Manager) Rutgers The State University of New JerseyTemporary Research Assistant (Junior Data Manager)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. Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption.
Research Project Interviewer - NJ - On Site SagoResearch Project Interviewer - NJ - On SiteIselin, NJThe Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation. Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success.
Research Associate Comparative Biosciences IncResearch Associatehamilton township, NJThe Institute for Biomarker Research (IBR), a division of GGG, is dedicated to the innovation of multi-variant-based personal diagnostics to assess disease evaluation, progression, regression, and patient stratification in order to establish a targeted, pharmacogenomic-based treatment approach tailored to every patients specific clinical situation. Job Summary: Genesis Global Group (GGG) is a consortium of entities and institutes, in the field of molecular biology, medicinal chemistry and biotechnology.
Associate Director, Clinical Operations Summit Therapeutics IncAssociate Director, Clinical OperationsPrinceton, NJ$174,000–$205,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Drafts, reviews and approves internal and external study-related plans, processes, and documents including Informed Consent Forms, Investigator Agreements (CTA), CRFs, CRF Guidelines, statistical/pharmacokinetic analysis plans, monitoring plans, data management plans, and safety monitoring activities.
Research Associate Comparitive Biosciences Inc.Research AssociateHamilton Township, NJThe Institute for Biomarker Research (IBR), a division of GGG, is dedicated to the innovation of multi-variant-based personal diagnostics to assess disease evaluation, progression, regression, and patient stratification in order to establish a targeted, pharmacogenomic-based treatment approach tailored to every patient's specific clinical situation. Job Summary: Genesis Global Group (GGG) is a consortium of entities and institutes, in the field of molecular biology, medicinal chemistry and biotechnology.
Research Associate LCMS, Bioanalysis & Microdialysis PsychoGenics IncResearch Associate LCMS, Bioanalysis & MicrodialysisParamus, NJOur mission is to provide the best validated disease models and comprehensive preclinical capabilities to help companies discover the next generation of treatments for severely disabling CNS and orphan disorders and reduce the attrition rate in clinical development. With an extensive portfolio of highly predictive disease models and unparalleled experience performing studies for biopharmaceutical companies of all sizes, we enable clients to deliver much needed superior clinical candidates to patients.
Director, Qualitative Market Research IPG MediaBrandsDirector, Qualitative Market ResearchDoylestown, PA$120,000–$150,000 / yearDemonstration of a deep understanding of the market research needs of pharmaceutical and biotech products in various stages of the product life cycle (Phase 2 through Phase 4 clinical trials, pre-launch promotional development, in-line/mature products). If you're looking for a company that strives to create a work environment that encourages and compliments you, you're curious, a critical thinker able to think outside the box, like challenges and are passionate about what you do, we definitely want to speak with you!
NewAssociate Director, Global Commercialization, Market Research Genmab ASAssociate Director, Global Commercialization, Market ResearchPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. The role will partner closely with Global Brand Teams, Regional and Local Market Research colleagues, Commercial leadership, Medical Affairs, Forecasting, Competitive Intelligence, and Alliance partners to design and execute primary market research programs that support strategic and tactical business decisions.
Senior Specialist, Research Manager Merck & Co IncSenior Specialist, Research ManagerRahway, NJ$106,200–$167,200 / yearRequired Skills: Data Analytics, Meeting Management, Observational Research, Problem Identification, Project Management, Project Team Management, Real World Data, Real World Evidence (RWE), Research Administration, Research Management. Ensure studies follow all non-interventional processes for informed consent, compliance, training, site contract and budget review/approval, protocol document review (including DRC), study registration (when applicable), adverse event reconciliation, change orders, publication submission, and study close out.
NewPrincipal Research Associate (Dr. Anita Kinney's Lab) Rutgers The State University of New JerseyPrincipal Research Associate (Dr. Anita Kinney's Lab)New Brunswick, NJEssential Duties and Responsibilities include the following: Ensures complex studies including observational, risk communication, behavioral and health services intervention research (involving biospecimens, genetic information, clinical and/or patient reported data) and implementation science projects in cancer patients and persons at risk for cancer, including socioeconomically disadvantaged and underserved racial and ethnic populations are administered as per study protocol, including enrolling and retaining study enrollees as per study timelines. MISSION: Our mission is to accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention; to provide outstanding, novel, and compassionate patient care; to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community; and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities.
Research Associate - IT Infrastructure Lead Rutgers The State University of New JerseyResearch Associate - IT Infrastructure LeadNew Brunswick, NJUnder Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. Experience working in data centers maintaining service uptime, including hardware installation and equipment moves, hardware networking, power consumption management, and interaction with data center personnel.
Clinical Trial Specialist Actalent IncClinical Trial SpecialistNew Brunswick, NJ$35–$38 / hourThis involves verifying approvals from the Scientific Review Board (SRB), Institutional Review Board (IRB), and Human Research Oversight Committee (HROC), as well as finalizing data collection plans and finance/contract approvals prior to study activation. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.