Senior Clinical Research Associate - CNS - Midwest (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS - Midwest (Remote)NYRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Lead Clinical Research Associate Integrated Resources, IncLead Clinical Research AssociateRaritan, New JerseyFull timeThe LCRA acts as a primary liaison between Field Based CRAs and the Clinical Project Lead (CPL).Additional responsibilities include:• Implementation of enrollment and recruitment strategies• Assistance in vendors' selection processes• Development, execution, management and compliance assurance of the Monitoring Plan• Review and approve trip reports, track scheduling, report submission metrics, site deviations and action items• Oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions.• Job DescriptionTitle: Lead Clinical Research AssociateLocation: Raritan, NJ 08869Responsibilities:Lead Clinical Research Associate:Under supervision of Clinical Project Lead, oversees performance of assigned field monitors and site activities in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal regulations.
Sr. Clinical Project Manager Integrated Resources, IncSr. Clinical Project ManagerSouth Plainfield, New JerseyContractorIt is a Contract-to-Hire position (the contract will last 90 days, after which the position will turn permanent provided the contract period is successfully completed).Will manage several (4-5) projects simultaneouslyMust have Pharma / BioPharma experience (any blood-based experience a plus)Able to interface with Clinicians, MD's, Finance and managementTrack/manage resources and project tasks and report status to managementMust have good communication skills to interface withMinimal US-based travel (10-15%).Job Clinical Project ManagerA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Sr. Director, Clinical Research Colgate-Palmolive CoSr. Director, Clinical ResearchPiscataway, NJ$250,000–$275,000 / yearEstablished in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such internationally recognized brand names as Colgate, Palmolive, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom's of Maine, Sanex, Ajax, Axion, Soupline, Haci Sakir, Suavitel, PCA SKIN, EltaMD, Filorga and Hello as well as Hill's Science Diet and Hill's Prescription Diet. Develop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products.
Senior Scientist, Clinical Research Merck & Co IncSenior Scientist, Clinical ResearchRahway, NJ$117,000–$184,200 / yearCo-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.
Senior Clinical Research Associate Zp Group LlcSenior Clinical Research AssociateNY$155,000–$175,000 / yearKeywords: clinical research, clinical trials, CRA, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk-based monitoring, therapeutic areas. The Senior Clinical Research Associate (CRA) will join a remote, contract-based team supporting Phase II and Phase III studies across a variety of general medicine indications within a full-service clinical research environment.
Phase I Oncology Clinical Research Associate Zp Group LlcPhase I Oncology Clinical Research AssociateNY$110,000–$140,000 / yearKeywords: Phase One Oncology CRA, Clinical Research Associate, Phase I Oncology, First-in-Human Trials, Dose Escalation, Oncology Clinical Research, GCP, FDA Regulations, Clinical Monitoring, Biotechnology, Pharmaceutical. Piper Companies is seeking a Phase I Oncology Clinical Research Associate to support early-phase oncology clinical trials within the biotechnology and pharmaceutical industry.
Clinical Project Lead, Oncology IQVIAClinical Project Lead, OncologyParsippany, GeorgiaIn this remote role you will serve as the primary country-level leader for clinical trial delivery , ensuring studies are executed efficiently from start-up through closeout. Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.
Oncology Clinical Research Nurse - JS Hope Tower - F/T Days Hackensack Meridian HealthOncology Clinical Research Nurse - JS Hope Tower - F/T DaysNeptune, New JerseyFull timeResponsibilities: Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.
Senior Program Manager - Medical & Clinical Affairs ConvaTec Group PlcSenior Program Manager - Medical & Clinical AffairsBridgewater, NJRemotePosition Overview: As part of the Project and Portfolio Management team for Medical and Clinical Affairs, the Sr Program Manager oversees the project management, planning, execution, tracking, and reporting of clinical studies and/or research projects in accordance with agreed upon resourcing, timing, and budget. Leader and team-worker who actively looks to develop themself and others; proactively networks across a complex organizational hierarchy and works cooperatively and effectively with others to set goals and resolve problems.
Senior Clinical Research Director SanofiSenior Clinical Research DirectorMorristown, NJ$236,250–$393,750 / yearCollaborates with other CRDs within the project, ensures leadership, builds consensus, coordinates action plans with stakeholders to resolve project-related study issues, anticipates potential issues (sharing lessons learned) across the project or study teams. Collaborate with other CRDs within the project, ensure leadership, buildsconsensus, coordinate action plans with stakeholders to resolve project-related study issues, anticipate potential issues (sharing lessons learned) across the project or study teams.
Senior Clinical Research Associate (Remote - Field Based) Novartis AGSenior Clinical Research Associate (Remote - Field Based)NYRemote$108,500–$201,500 / yearKey ResponsibilitiesLead assigned sites as the primary point of contact throughout study deliveryBuild strong relationships to ensure site performance, quality, and milestone achievementManage Phase I to Phase IV trials per monitoring plans and company proceduresConduct site initiation visits and deliver ongoing training for site personnelPerform remote and on-site monitoring to ensure compliance and patient safetyMaintain accurate documentation and update all clinical systems in a timely mannerIdentify risks, resolve issues, and escalate concerns as neededCollaborate with cross-functional teams to drive efficient study executionSupport timely data query resolution and ensure data accuracyAct as a subject matter expert across study activities when requiredEssential RequirementsMinimum of three years of clinical site monitoring experienceMinimum of Bachelor's degree in science, healthcare, or a related fieldStrong understanding of clinical research and drug development processesKnowledge of ICH/GCP and 21 CFR regulatory requirementsAbility to manage multiple priorities and work independentlyStrong site management, communication, and problem-solving skillsFluency in English, written and spoken, Spanish highly desiredAbility to drive and travel extensively, up to 80%, in a company vehicleDesirable RequirementsExperience in multiple therapeutic areas and Veeva Vault CTMS is a plus Advanced knowledge and use of AI The salary for this position is expected to range between $108,500 and $201,500 per year. Assigned to complex trials and/or less experienced sites, you may also act as a Subject Matter Expert, support audit and inspection readiness activities, ensure timely implementation of corrective actions, and collaborate with local and global cross-functional teams to drive process improvements that help bring innovative therapies to patients faster.
Senior Manager, Clinical Scientist Gan & Lee PharmaceuticalsSenior Manager, Clinical ScientistNJFull timeExperiences in metabolic diseases (Diabetes, Obesity, NASH, NAFLD, etc.), Endocrinology (CKD, CRF, etc.), and Nutrition and Weight Management related drug development are a plus. The position will work with Gan & Lee clinical program lead(s) to provide the scientific and clinical leadership and inputs in meeting the development objectives for the program.
Clinical Research Director - Rare Diseases SanofiClinical Research Director - Rare DiseasesMorristown, NJ$178,500–$257,833.33 / yearExperience / Skills: MD or MD/PhD in a relevant scientific discipline, preferably pulmonology, with at least 2 years relevant experience in clinical development within the pharmaceutical industry, academia, or government agencies such as the NIH, FDA, or other equivalent national or international public health and regulatory organization. On Clinical Development, the CRD: Designs the global clinical development strategy (in close cooperation with other members of the team, particularly Regulatory Affairs end Health Economics) and leads the clinical development with regard to ongoing development activities and planned LCM for labelling changes.
Clinical Research Director, Rare Diseases SanofiClinical Research Director, Rare DiseasesMorristown, NJ$206,250–$343,750 / yearExperience / Skills: MD or MD/PhD in a relevant scientific discipline, preferably pulmonology, with at least 2 years relevant experience in clinical development within the pharmaceutical industry, academia, or government agencies such as the NIH, FDA, or other equivalent national or international public health and regulatory organization. On Clinical Development, the CRD: Designs the global clinical development strategy (in close cooperation with other members of the team, particularly Regulatory Affairs end Health Economics) and leads the clinical development with regard to ongoing development activities and planned LCM for labelling changes.
Clinical Research Associate II/III Novotech Health Holdings Pte LtdClinical Research Associate II/IIINY$70,000–$140,000 / yearPreferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience (CRA II fast track) in other roles in the Clinical industry. Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs.
Sr. Director, Clinical Research (Piscataway, NJ, US) Colgate-Palmolive CompanySr. Director, Clinical Research (Piscataway, NJ, US)Piscataway, NJ$250,000–$275,000 / yearDevelop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products. The ideal candidate is an internationally renowned expert in oral health and dental clinical research, with substantial industry and/or academic experience, a proven track record of leading clinical programs, and demonstrated strength in people leadership and collaborative partnerships.
Principal Scientist, Clinical Research - Immunology/Dermatology Merck & Co IncPrincipal Scientist, Clinical Research - Immunology/DermatologyRahway, NJ$255,800–$402,700 / yearAssist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead in ensuring that appropriate corporate personnel is informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.
Clinical Project Associate OrganOxClinical Project AssociateMadison, NJRemote$60,000–$75,000The CPA contributes to ongoing studies by performing on-site monitoring visits and remote monitoring visits (with oversight); centralized monitoring, following up on monitoring visit action items; maintaining in-house study files; providing day-to-day study management and site support; interfacing with site coordinators, investigators, field clinical staff, and other company representatives. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant.
Clinical Research Associate (CRA) Zp Group LlcClinical Research Associate (CRA)NYRemote$155,000–$175,000 / yearThe Clinical Research Associate (CRA) role is ideal for an experienced monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol compliance across multi-site trials. Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry.