- Organon & Co. (Jersey City, NJ)
- **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more
- Parexel (Trenton, NJ)
- …requirements. **Responsibilities** + Focus on exploratory work to generate evidence supporting clinical trial design, including outcome summaries and insights + ... outcomes. We are seeking a passionate and experienced **RWE** Specialist join our team and support the design and...data standards. + Good understanding of regulatory requirements & clinical trial design is preferred. **Why Parexel?**… more
- Principal Financial Group (New York, NY)
- …detailed proprietary analysis of therapeutics companies globally leveraging: + comprehensive clinical pipeline, trial data, commercial forecasting / competitive ... market positioning assessments + relevant medical and scientific publications / meeting updates + FDA regulatory developments and policy actions / announcements + Interact frequently with company management, industry experts, and other stakeholders to gather… more
- Parexel (Trenton, NJ)
- …work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected ... Works with Precision Medicine Strategy Lead as well as clinical study teams, data management (DM) team, Samples, Kits,...stakeholders, such as working with Informed Consent Form (ICF) specialist in SKDL on ICF and other trial… more
- Parexel (Trenton, NJ)
- … clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** **Study Team Support** + ... collection procedures and presentation slides) + Manages acquisition of clinical trial samples + Provides support for...study teams + Works with Informed Consent Form (ICF) Specialist and Precision Medicine Operations Lead (PMOL) to ensure… more
- Parexel (Trenton, NJ)
- …in Lupus is preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
- Actalent (Newark, NJ)
- Job Title: Clinical Trial Specialist Job Description As a Clinical Trial Specialist , you will coordinate the initiation and activation of new ... clinical trial protocols. This role involves verifying necessary approvals from various boards and committees, preparing study tools, and ensuring that all… more
- Sumitomo Pharma (Trenton, NJ)
- …on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring ... that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and inspections....for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable… more
- J&J Family of Companies (Raritan, NJ)
- …more at https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical Trial Project Management **Job Category:** Professional **All Job ... related industries. (Required) + Strong Project Management experience (preferably in clinical trial management). (Preferred) + Experience leading without… more
- Sanofi Group (Morristown, NJ)
- …than 80 countries so that trial implementation is not disrupted. As a Clinical Supply Optimization Specialist (CSOS) within the CSC-PM team, you will be ... **Job Title:** Clinical Supply Optimization Specialist **Location** :...supplies needed to conduct any Sanofi Pharma and Vaccines clinical trial are set up, planned, ordered,… more
- Merck (Rahway, NJ)
- …as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent must ... not limited to:** + Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area representatives to… more
- Merck (Rahway, NJ)
- … **Primary activities include, but are not limited to:** - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area ... Operations etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and Global - Development Quality (GDQ)… more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …occupational series. For more information, refer to Required Documents below. The Clinical Pharmacy Practitioner functions as a therapeutic expert in drug use and ... rounds Responsible for daily performance and oversight of provider-consulted, clinical pharmacy pharmacokinetic monitoring program for hematology/oncology patients. This… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to ... adjusted when new or unanticipated issues arise once the trial has begun. **Key Responsibilities:** + Develop the Quality...with the CAPA CoE and Serious Breach pillar and Clinical Quality Assurance to gather input from audits, inspections,… more
- ICON Clinical Research (New York, NY)
- …with Echo Tech experience, looking for an exciting opportunity to work with a Clinical Trial environment? Are you looking for a role that will combine ... required for maximizing medical data and information used in clinical trials. ROLE OVERVIEW + The Imaging Specialist... clinical trials. ROLE OVERVIEW + The Imaging Specialist is responsible for daily image quality review, image… more
- Deloitte (Princeton, NJ)
- …clients within the Life Sciences & Healthcare sector, utilizing Veeva Vault Clinical Trial Management Systems (CTMS), Regulatory Information Management ( RIM) ... of health. Work you'll do As an Industry Solutions Specialist Leader you will lead the creation of innovative...Suite, and electronic Trial Master File (eTMF) + 6+ years of experience… more
- Merck (Rahway, NJ)
- …Skills:** Accountability, Accountability, Adaptability, Change Management, Clinical Development, Clinical Research, Clinical Trial Management, ... direction from the Director/Associate Director Publication Management, the Sr. Specialist Publication Manager coordinates publication planning and implementation, tracks… more
- Veterans Affairs, Veterans Health Administration (Kings County, NY)
- …for accepting this position, you will be required to serve a 2 year trial period during which we will evaluate your fitness and whether your continued employment ... efficiency of the Federal service. Upon completion of your trial period, your employment will be terminated unless you...rehabilitation. The work environment may be in an office, clinical setting, classroom, private home, VA grounds, nursing home,… more
- Norstella (Trenton, NJ)
- …& analytics **Requirements** + Deep knowledge and expertise of the pharma strategic Clinical trial landscape (Clin Dev/Ops, clinical development plan ... within Sponsor/CRO/Partner environment + Experience using data analytics and services to solve clinical trial challenges + Understanding of how, and where, AI… more
- Bausch + Lomb (Trenton, NJ)
- …ensuring alignment with global requirements. + Provide guidance on risk assessment, clinical trial design implications, and regulatory pathways. + Support ... regulatory strategies for development programs and marketed products across CMC and clinical /non- clinical , labeling, adpromo areas. Serve as a strategic advisor… more
