On-site Clinical Research Associate Protagonist TherapeuticsOn-site Clinical Research AssociateNewark, New JerseyThe Company also has a number of clinical and preclinical programs based on clinically and commercially validated targets and addressing unmet medical needs, including an oral IL-17 antagonist peptide, anti-obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin discovery programs. Clinical Research Associate About Us Protagonist Therapeutics is a biopharmaceutical company built on a proprietary peptide technology platform that has now produced two FDA-approved, first-in-class medicines, generating royalties and milestones from global commercial partnerships with Johnson and Johnson and Takeda Pharmaceutical Company Limited.
Home Care Clinical Supervisor Honor Health NetworkHome Care Clinical SupervisorRidgefield Park, New JerseyRemote$50,000–$70,000 / yearTech-Savvy: Proficiency with Home Health Electronic Medical Record (EMR) software (e.g., Axxess, Homecare Homebase, KanTime) and digital communication tools (Slack, Zoom, Microsoft Teams). We are a premier skilled nursing home care agency seeking a Lead Nurse Scheduling & Clinical Coordinator to oversee our field nursing schedules, streamline our human resources onboarding, and drive clinician retention.
Clinical Research Coordinator - Albuquerque, NM IQVIAClinical Research Coordinator - Albuquerque, NMParsippany, New MexicoAs a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study‑related procedures, and ensuring adherence to study protocols and regulatory requirements. This role is well‑suited for a detail‑oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high‑quality clinical research within diverse communities.
Licensed Clinical Supervisor Community Psychiatric InstituteLicensed Clinical SupervisorEast Orange, NJ$70,000–$90,000 / yearFull timeCommunity Psychiatric Institute, a leader in Behavioral Healthcare and Chemical Dependency treatment for over 54 years in Essex County, is seeking an innovative & dedicated individual to work full-time as the Clinical Supervisor in our adult psychiatric Partial Care program. CPI’s mission is to provide evidenced-based, person centered care in order to improve the quality of life for individuals struggling with mental health and substance use disorders.
Clinical Research Assistant Adams ClinicalClinical Research AssistantNew York, NY$24–$29 / hourWorking under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
Neurologic Music Therapist - Clinical Internship - Burke MEDRhythmsNeurologic Music Therapist - Clinical Internship - BurkeWhite Plains, NYFounded in 2015, MedRhythms has partnered with leading rehabilitation hospitals, including Spaulding Rehabilitation Hospital, Burke Rehabilitation Hospital, and JFK Johnson Rehabilitation Institute, to build some of the nation's most comprehensive NMT programs. As we continue to grow our clinical services and innovative rehabilitation technologies, we remain committed to clinical excellence, collaboration, and expanding access to life changing neurologic care.
Patient Recruiter/Clinical Research Prism Vision GroupPatient Recruiter/Clinical ResearchNew Providence, New JerseyThe CRR partners with research coordinators, physicians, office staff, and sponsors to identify potential clinical trial participants, conduct preliminary qualification reviews, and facilitate timely referral of eligible patients to site research teams. The Clinical Research Recruiter I (CRR) is responsible for supporting centralized patient recruitment and pre-screening activities across Prism Vision Group's network of ophthalmology research sites.
Lead Clinical Application Analyst Macpower Digital Assets Edge Private LimitedLead Clinical Application AnalystNew York City, NY$97,000–$145,000 / yearProvides programming support for the relevant departmental systems, subsystems, and related software products, in supports of clinical and operational clients. Develops, test, documents and implements changes and enhancements to existing interfaces, supports scripts, or other changes to the interface engine environment.
Global Clinical Study Senior Manager BeOne Medicines AGGlobal Clinical Study Senior ManagerNY$136,400–$181,400 / yearEnsures that the clinical study is operationally feasible in all regions, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders. This role serves as the primary global operational owner, responsible for aligning cross-functional stakeholders, managing global study strategy execution, and driving performance against timelines, quality, and budget.
Clinical Laboratory Technologist - Biochemistry New York University School of MedicineClinical Laboratory Technologist - BiochemistryNew York, NY$101,555.94–$127,619.35 / yearFollows approved guidelines in approaches to problem solving and devises appropriate courses of action when patient results, control values and instrument function parameters are inconsistent or invalid: including investigation of possible sources of variance/interference, by taking appropriate action and/or performing additional testing as necessary to assure the accuracy of the reported patient value. Bachelors Degree in Clinical Laboratory Technology from a program registered by the NYS Department of Education or Bachelors Degree in the major of biology, chemistry or physical sciences from an accredited college or university or education requirement grandfathered by the NYSOP.
Clinical Database Designer I Everest Clinical ResearchClinical Database Designer INew JerseyRemoteEverest Clinical Research (“Everest”) is a full-service, global, contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Follow up on regulatory requirements, industry trends, benchmarking, and best working practices in data management and database design by reading, participating in relevant training, and/or associated activities.
Clinical Pharmacotherapy Specialist - Adult Transplant Services New York University School of MedicineClinical Pharmacotherapy Specialist - Adult Transplant ServicesNew York, NY$195,889.94–$218,517.47 / yearhas ranked NYU Langone the No. 1 comprehensive academic medical center in the country for three years in a row, and U.S. News & World Report recently placed nine of its clinical specialties among the top five in the nation. With $14.2 billion in revenue this year, the system also includes two tuition-free medical schools, in Manhattan and on Long Island, and a vast research enterprise with over $1 billion in active awards from the National Institutes of Health.
Clinical Research Nurse Adams ClinicalClinical Research NurseNew York, NY$90,000–$110,000 / yearThis position will also involve general research-related responsibilities like facilitating the informed consent process, administration of screening procedures, data entry, maintenance of regulatory binders, and other nursing functions as required in support of the clinical trial. As a member of our clinical team, you will work under the supervision of our physician principal investigators and clinical nurse manager on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines.
Clinical Laboratory Technologist - Part Time New York University School of MedicineClinical Laboratory Technologist - Part TimeNew York, NY$55.80–$69.55 / hourFollows approved guidelines in approaches to problem solving and devises appropriate courses of action when patient results, control values and instrument function parameters are inconsistent or invalid: including investigation of possible sources of variance/interference, by taking appropriate action and/or performing additional testing as necessary to assure the accuracy of the reported patient value. Bachelors Degree in Clinical Laboratory Technology from a program registered by the NYS Department of Education or Bachelors Degree in the major of biology, chemistry or physical sciences from an accredited college or university or education requirement grandfathered by the NYSOP.
Clinical Research Coordinator - Somerset, NJ IQVIAClinical Research Coordinator - Somerset, NJParsippany, New JerseyThis role plays a critical part in the successful execution of clinical trials, combining hands-on clinical procedures, patient interaction, and study coordination to ensure compliance, data integrity, and participant safety. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that accelerate innovation and improve patient outcomes worldwide.
Clinical Lab Technologist - Part Time - Biochemistry New York University School of MedicineClinical Lab Technologist - Part Time - BiochemistryNew York, NY$55.80–$70.12 / hourIn this role, the successful candidate performs all routine and complicated laboratory procedures including specimen processing and handling, testing of patient specimens, calculating and reporting of results, performance of quality control procedures, operation and maintenance of instruments and equipment. Bachelors Degree in Clinical Laboratory Technology from a program registered by the NYS Department of Education or Bachelors Degree in the major of biology, chemistry or physical sciences from an accredited college or university or education requirement grandfathered by the NYSOP.
NewClinical Research Associate - Sponsor Dedicated IQVIAClinical Research Associate - Sponsor DedicatedParsippany, KansasIn this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.
Clinical Resource Nurse, Mother/Baby, Night Shift *experience required* New York University School of MedicineClinical Resource Nurse, Mother/Baby, Night Shift *experience required*New York, NY$132,017.38–$156,767.38 / yearAs a member of the interdisciplinary healthcare team, formulates the initial plan of care with the provider (physician or nurse practitioner) and collaborates with them to implement a comprehensive patient-centered plan of care to achieve expected outcomes; utilizes principles of assignment and delegation consistent with the NY State Nurse Practice Act. Minimum Qualifications: To qualify you must have a Current Registered Professional Nurse in New York, Bachelors degree in Nursing from an accredited institution required, Basic Life Support Certification through the American Heart Association, Fluent written and spoken English language skills.
Clinical Research Coordinator - Union, SC IQVIAClinical Research Coordinator - Union, SCParsippany, South CarolinaThe actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Director/Sr. Director/Executive Director, Clinical Regulatory Affairs Systimmune IncDirector/Sr. Director/Executive Director, Clinical Regulatory AffairsPrinceton, NJ$200,000–$300,000 / yearThe Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department in all aspects of global regulatory affairs related to development of novel oncology therapeutics (multiple modalities such as ADCs, bispecific antibodies and T-cell engagers etc.). Own/drive the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: BLA/INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator's Brochure.