- Merck & Co. (Rahway, NJ)
- …within Fair Market Value based upon protocol design, industry benchmark data and clinical trial team feedback.Represent Global Site Budgets and Payments on ... dedicated colleagues while developing and expanding your career.The Senior Trial Initiation Specialist in Global Site Budgets...Clinical Trial Teams during trial … more
- Merck & Co. (Rahway, NJ)
- …pharmacokinetic, exposure-response, quantitative system pharmacology, and other model-based analyses.-Perform clinical trial simulations to inform dose selection ... the-Quantitative Pharmacology and Pharmacometrics --Immune/Oncology-(QP2-IO)-team in the role of-Senior Specialist .--QP2-IO team is part of the Global Clinical … more
- Merck & Co. (Rahway, NJ)
- …The Specialist will be responsible for: Authoring scientifically valid clinical trial registration and results postings on www.ClinicalTrials.gov (United ... Writing & Disclosure Department of the GCTO ( Global Clinical Trial Operations) organization prepares a variety... development portfolio and compliance in public disclosure of clinical trials and their results, document disclosure,… more
- J&J Family of Companies (New Brunswick, NJ)
- …execution of study operational plans as it relates to imaging for clinical trials . + Work closely with all cross-functions trial teams ( Clinical , Stats, ... Director, Clinical Scientist - Imaging Specialist (INTO)...+ Proven track record of successfully leading and managing clinical trials with a strong understand of… more
- Vitalief (New Brunswick, NJ)
- …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high… more
- Merck (Rahway, NJ)
- …and new indications for existing products. We ensure we conduct high-quality clinical trials by integrating state-of-the-art technology and applying rigorous ... Participate in standards data governance reviews + The Global Clinical Data Standards (GCDS) Data Standards Specialist ...Global Clinical Data Standards (GCDS) Data Standards Specialist may contribute to the definition and maintenance of… more
- Philips (New Brunswick, NJ)
- …products and company product enhancements + Provides ongoing support for company-sponsored clinical /marketing trials and registries **You're the right fit if:** ... + You've acquired 3+ years direct experience in a hospital setting + Your skills include a license as a Cardiovascular Radiologic Technologist (CRT), Cardiovascular Technologist (CVT), or Registered Nurse (RN) or CVIS, RCIS + You have a High School diploma;… more
- Vitalief (Newark, NJ)
- …weekend work could be required. Responsibilities: + Reporting to a Clinical Trial Recruitment Team Lead, the Recruitment Specialist will work with the Team ... Healthcare consulting company, focused on empowering Research and transforming Clinical Trials . We are working on a...with Rutgers University and seeking several talented and enthusiastic Clinical Trial Recruitment Specialists to join our… more
- Merck (Rahway, NJ)
- … clinical supply chain across the full company Research Laboratories portfolio of clinical trials . GCS supports more than 300 Phase I-IV clinical ... by partners, and 300+ company Investigator Initiated Studies (IIS) clinical trials . GCS is accountable for the...spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related… more
- Merck (Rahway, NJ)
- …within Fair Market Value based upon protocol design, industry benchmark data and clinical trial team feedback. + Represent Global Site Budgets and Payments ... colleagues while developing and expanding your career. **The Senior Trial Initiation Specialist in Global Site Budgets...on Clinical Trial Teams during trial … more
- Medtronic (Morristown, NJ)
- …RESPONSIBILITIES:** The following responsibilities are to be performed as appropriate in clinical trial case support and/or case support following commercial ... EKG, blood pressure, wave forms, and ancillary procedural solutions + Knowledge of Clinical trial protocols, and CoreValve and other Medtronic TAVR product IFUs… more
- Hackensack Meridian Health (Nutley, NJ)
- …for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant ... general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities**...+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist … more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …PharmD, PA, APRN, or RN depending on Industry experience. + At least 5 years of clinical trial experience + At least 5 years of medical device industry and/or ... and reports directly to the VP, GMS&G. **Responsibilities:** + Co-manage and support Clinical Safety Specialist (CSS) for their respective BU + Responsibility in… more
- Novo Nordisk (Princeton, NJ)
- …with teams in departments throughout the organization, including Medical Affairs, HEOR, Clinical Trial Management, Market Development & HCP Engagement, as well ... the head of Rapid Cycle Analytics (RCA) and functions as an analytics specialist in the Clinical Data Science & Evidence (CDSE) department. Collaborates closely… more
- System One (Plainsboro, NJ)
- …a Senior Retention Specialist to support patients enrolled in the clinical trials . Ideal candidates will have a Nursing/Physician Assistant background and ... Job Title: Senior Retention Specialist Location: Hybrid schedule onsite 3x/week in Plainsboro,...trials . + A minimum of 5 years of clinical trial experience within a pharmaceutical, biotechnology,… more
- Hackensack Meridian Health (Hackensack, NJ)
- …**Start Up Specialist ** is responsible for the oversight and management of clinical trial start-up activities and serves as a primary contact for ... A day in the life of a **Start Up Specialist ** at Hackensack Meridian _Health_ includes: + Manages all...and Execution of Confidentiality Agreements, Material Transfer Agreements and Clinical Trial Agreements. + Independently oversees … more
- Hackensack Meridian Health (Hackensack, NJ)
- …oversight and management of clinical trial regulatory for all assigned clinical trials and serves as a primary contact for investigators and research ... positive change. The **Senior Regulatory Specialist ** is responsible for the...clinical trial lifecycle for all assigned clinical trials . **Responsibilities** A day in the… more
- Actalent (Hackensack, NJ)
- …the Review and Execution of Confidentiality Agreements, Material Transfer Agreements and Clinical Trial Agreements. Independently oversees Clinical Trial ... Principal Investigator (PI) by providing administrative support to develop, implement and complete clinical trial submissions. Prepares clinical trial … more
- Actalent (Hackensack, NJ)
- …the Review and Execution of Confidentiality Agreements, Material Transfer Agreements and Clinical Trial Agreements. + Independently oversees Clinical ... Principal Investigator (PI) by providing administrative support to develop, implement and complete clinical trial submissions. + Prepares clinical trial … more
- Hackensack Meridian Health (Hackensack, NJ)
- …documentation throughout the clinical trial lifecycle for all assigned clinical trials . **Responsibilities** A day in the life of a **Regulatory ... as it relates to all regulatory aspects of assigned clinical trials conduct. This role will serve...the Medicare Coverage Analysis, budget and contract for a clinical trial in order to initiate a… more
