Bilingual Clinical Research Coordinator Actalent IncBilingual Clinical Research CoordinatorNew Brunswick, NJ$25–$33 / hourThis role offers an opportunity for an experienced bilingual Clinical Research Coordinator to support a clinical trial at a research site by managing patient recruitment, conducting chart reviews, and ensuring accurate and timely data entry and query resolution. 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.
Senior Clinical Research Scientist Legend Biotech CorpSenior Clinical Research ScientistSomerset, NJ$127,313–$167,099 / yearHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. Contribute to the planning and execution of external meetings and internal stakeholder meetings (e.g., Ad Boards, IMs, Governance, DMCs, Regulatory Authority, Dose Escalation meeting); responds to or triages questions for appropriate escalations.
Executive Medical Director Summit Therapeutics IncExecutive Medical DirectorPrinceton, NJ$291,000–$364,000 / 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. He/she will be responsible for obtaining scientific advisory input, work with biostatisticians for Phase 3 design and analyses, support regulatory interactions for product advancement, and work closely with clinical operations to provide advice and decision making regarding medical input to achieve operational excellence.
Clinical Trial Specialist Actalent IncClinical Trial SpecialistNew Brunswick, NJ$35–$38 / hourCoordinate the initiation and activation of new clinical trial protocols, ensuring all required approvals are in place before study activation, including Scientific Review Board, Institutional Review Board, Human Research Oversight Committee, data collection plans, and finance/contract approvals. This role ensures that all regulatory, ethical, and operational requirements are met, while working closely with research nurses, physicians, and study sponsors to deliver high-quality, compliant research that advances cancer care.
Assistant/Associate Professor Behavioral Neurology Rutgers The State University of New JerseyAssistant/Associate Professor Behavioral NeurologyNew Brunswick, NJThe specific benefits vary based on the position and may include: • Medical • Prescription drug and dental coverage • Paid vacation • Holidays • Various leave programs • Competitive retirement benefits including defined contribution plans and voluntary tax-deferred savings options • Employee and dependent educational benefits when applicable • Life insurance coverage • Employee discount programs. Immunization Requirements 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.
Division Chief, Surgical Oncology (Associate Professor - Professor Rank) Rutgers The State University of New JerseyDivision Chief, Surgical Oncology (Associate Professor - Professor Rank)New Brunswick, NJTo 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. The Division Chief will work under the direction of Rutgers Cancer Institute's Chief Surgical Officer and Director on mutually agreed upon areas and serve as the liaison to Robert Wood Johnson University Hospital and the RWJBarnabas Health Oncology Service Line for all operational and programmatic matters regarding surgical oncology programs for the Rutgers Cancer Institute.
Tumor Immunology - Tenure Track (Assistant Professor Rank) Rutgers The State University of New JerseyTumor Immunology - Tenure Track (Assistant Professor Rank)New Brunswick, NJTo 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. Rutgers Cancer Institute invites applications for a tenure-track assistant professor faculty position with a research focus in tumor immunology including cancer immunotherapy, immunometabolism, CAR-T therapy, checkpoint blockade, T cell biology, tumor antigens, tumor immune evasion, and viral and non-viral gene transfer and gene editing.
Associate Scientific Director Clinical Development - Endocrinology Recordati SpAAssociate Scientific Director Clinical Development - EndocrinologyBridgewater, NJThey are involved in delivering almost all aspects of externally facing medical communications and serve as subject matter expert for other roles in medical affairs (MA).\n \nEssential Duties and Responsibilities\n \nThe Associate Scientific Director is directly responsible for delivering the following:\n\n Contributing to the Clinical Development plan, including identifying critical data gaps, defining evidence needs to support scientific objectives and key messages, and proposing data generation strategies that feed into the Scientific Data Evolution Plan.\n Supporting clinical trial protocol development as an endocrinology subject matter expert (SME), providing scientific and clinical guidance to ensure robust study design, methodological rigor, and alignment with clinical development objectives.\n Unlocking the full potential of life.\n \nThis position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati.\n \nRecordati Rare Diseases, Inc. (RRD) develops high-impact therapies for rare diseases, focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, better diagnoses, and improved treatment access in endocrinology, metabolic, hematology and oncology franchises.
Executive Director, Pipeline Clinical Lead Legend Biotech CorpExecutive Director, Pipeline Clinical LeadSomerset, NJ$294,483–$386,511 / yearHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. This role provides strategic and operational leadership across first in human through proof of concept studies, with accountability for clinical strategy, trial design, execution, interpretation, and regulatory interactions.
Assistant /Associate Professor Movement Disorder Rutgers The State University of New JerseyAssistant /Associate Professor Movement DisorderNew Brunswick, NJESSENTIAL DUTIES AND RESPONSIBILITIES The faculty member will: • Be Board-certified or -eligible in neurology • Have completed a fellowship in movement disorders and be eligible for a New Jersey license • Maintain a practice in the full range of adult movement disorders neurology • To maintain a full schedule while building a referral network, the faculty member may be required to see some patients with neurological conditions other than movement disorders • Have skills in botulinum treatment for movement disorders and include such patients in the practice • Have skills in evaluation and medical management of patients who are candidates for deep brain stimulation and ablative surgery for movement disorders and in their postoperative management and stimulator programming • Must coordinate care with neurosurgery, psychiatry, and other disciplines as needed • Perform night call and weekend inpatient coverage at Barnabas-Robert Wood Johnson University Hospital in equal proportion with the other faculty in rotation • Participate in the teaching mission of RWJMS to the extent determined in consultation with the Department Chair • This may include teaching and mentoring medical students, neurology residents, movement disorder fellows, and rotators from other departments • The teaching will take place in inpatient and outpatient settings and in seminars and occasional formal lectures in the pre-clinical setting • It may also include supervising a weekly resident Continuity Clinic • Participate as site principal investigator or sub-investigator in clinical trials sponsored by industry and other sources • Perform and publish other research to the extent consistent with the track of the appointment Professional Practice Clinical Educator or Clinical Scholar • Refer patients as appropriate to clinical trials and other research activity in the department and otherwise participate in the scholarly productivity and culture of the department • Participate in community service responsibilities of the department in such areas as providing neurological care for indigent patients and teaching or advising lay community groups in multiple areas relating to movement disorders, including deep brain stimulation, in coordination with the Department of Neurosurgery • Participate in the administrative tasks of the department and medical school • This will include membership in standing or ad hoc departmental and institutional committees as determined in consultation with the Chair and according to RWJMS By-Laws and attending departmental and institutional faculty meetings • Maintain knowledge through continuing education and by maintaining Board certification in neurology and any relevant subspecialty certification. The specific benefits vary based on the position and may include: • Medical • Prescription drug and dental coverage • Paid vacation • Holidays • Various leave programs • Competitive retirement benefits including defined contribution plans and voluntary tax-deferred savings options • Employee and dependent educational benefits when applicable • Life insurance coverage • Employee discount programs.
Postdoctoral Associate (Singson) Rutgers The State University of New JerseyPostdoctoral Associate (Singson)New 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. The Singson laboratory at the Waksman Institute of Microbiology is seeking a postdoctoral associate to participate in our studies of reproductive biology in the C.elegans model system.
NewSenior Clinical Trial Manager Genmab ASSenior Clinical Trial ManagerPrinceton, 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. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.
New2nd Shift Laboratory Specialist - Extractions Actalent Inc2nd Shift Laboratory Specialist - ExtractionsPiscataway, NJThe position provides professional-level technical support in a high-throughput molecular biology and clinical research environment, performing and overseeing multistage purifications, nucleic acid extractions, and related assays to support genetic and biochemical studies. At least three months of documented laboratory training in each specialty in which the individual will perform high-complexity testing, or willingness to complete a three-month training period prior to independent sign-off if such training is not already documented.
NewLaboratory Specialist - Extractions Actalent IncLaboratory Specialist - ExtractionsPiscataway, NJThe position provides professional-level technical support in a high-throughput molecular biology and clinical research environment, performing and overseeing multistage purifications, nucleic acid extractions, and related assays to support genetic and biochemical studies. At least three months of documented laboratory training in each specialty in which the individual will perform high-complexity testing, or willingness to complete a three-month training period prior to independent sign-off if such training is not already documented.
Senior Manager, Field Medical Affairs-Neurology (mid-Atlantic states) Regeneron Pharmaceuticals IncSenior Manager, Field Medical Affairs-Neurology (mid-Atlantic states)Trenton, NJ$150,500–$245,500 / yearSupport clinical research activities throughout the life cycle (phase 1-4), as well as Investigator Initiated Studies, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ experts and sites in alignment with Medical Affairs objectives. To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) along with a minimum of 3-5 years related work experience preferred (clinical, managed care, or industry experience) including experience as a Medical Science Liaison.
Associate Director, Compliance & Ethics Investigations Bristol-Myers Squibb CoAssociate Director, Compliance & Ethics InvestigationsPrinceton, NJ$157,080–$190,344 / yearProven successful investigation/project management in developing and executing all phases of an investigation plan including: collection, review and analysis of data, information and records; conducting interviews; documenting work completed; drafting findings and conclusions; accountability for successful completion. 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.
Director/Senior Director, Clinical Development SystImmune, Inc.Director/Senior Director, Clinical DevelopmentPrinceton, NJ$230,000–$300,000 / yearSystImmune is seeking an experienced Director/Senior Director of Clinical Development to lead the direction, planning, execution, and interpretation of clinical trials within the Clinical Development program. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Director Biostatistics in Princeton, New Jersey, United States of America | Development Operations at Genmab Government of DenmarkDirector Biostatistics in Princeton, New Jersey, United States of America | Development Operations at GenmabPrinceton, NJDirector Biostatistics in Princeton, New Jersey, United States of America | Development Operations at Genmab Skip to main content Skip to main content Healthcare Professionals Patients & Care Partners Partnerships Contact Working at Genmab Career Areas Application Process Locations Talent Community Job Search Corporate Sign in Close the popup Sign in to Phenom Careers Enjoy a personalized jobs search Sign in with Google Employee Login Sign in with Google Sign up Saved jobs (0) Healthcare Professionals Patients & Care Partners Partnerships Contact Saved jobs (0) Toggle navigation - - Recruitment Fraud Warning: Please note that Genmab never requests payment, banking details, or Social Security numbers during the recruitment process. Close Covid-19 banner Director Biostatistics Category Development Operations Job Id R17259 Remote This job available in 3 locations Princeton, New Jersey, United States of America Copenhagen, Capital, Denmark Utrecht, Netherlands Save Apply Now We are extra[not]ordinary*(ex· tra· not· or· di· nary |\ ik- str-not- r-d - ner- ) Adjective: A unique word for Genmab meaning to go way beyond what is usual; to be remarkable; proudly unique and authentic Back to search results Previous job Next job JOB DESCRIPTION At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases.
Global Head, Scientific Communication and Publications - Oncology Johnson & JohnsonGlobal Head, Scientific Communication and Publications - OncologyRaritan, New JerseyThe position partners closely with Global Medical Affairs Leaders (GMALs), Strategy & Execution Leads (SELs), Clinical Development Teams (CDTs), R&D, Market Access, and regional leadership to integrate scientific communications with evidence generation and medical strategy, supporting engagement with internal stakeholders (e.g., Field Medical, Market Access) and external stakeholders (e.g., healthcare professionals, investigators). Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Digital Culture, Digital Literacy, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Process Optimization, Product Strategies, Stakeholder Analysis, Strategic Thinking .
Clinical Research Nurse VitaliefClinical Research NurseNew Brunswick, NJFull timeDeliver high-quality, compassionate, hands-on oncology nursing care while coordinating closely with investigators, clinical teams, and ancillary departments (e.g., pathology, radiology, clinical laboratory, surgery, infusion services) in accordance with study protocols, treatment plans, and Good Clinical Practice (GCP) guidelines. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.