- Abbott (New York, NY)
- …of the Clinical Sales Specialist (CSS) role is to provide TAVI clinical trial and commercial case support, trial enrollment & education initiatives ... accounts within a defined region. In this role, the Clinical Sales Specialist will be an integrated...On** This position is responsible for the following TAVI clinical trial & commercial activities with key… more
- Edwards Lifesciences (New York, NY)
- …**Case Support** + Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff and clinical ... research coordinators by providing on-site, real-time guidance during clinical trial implants, including contingency planning to address unforeseen occurrences… more
- Medtronic (New York, NY)
- …systems by being accountable, having a voice, and taking action. In this clinical specialist role, you will have additional responsibility providing support for ... within assigned territory(** **ies** **). To find all CRDN Clinical Specialist roles available please use #CRDNCS... clinical evaluation strategy; may provide input to clinical trial design + Identify potential evidence… more
- Merck (Rahway, NJ)
- …activities include, but are not limited to:** + Participates on the Clinical Trial Team(CTT)and collaborates closely with other functional area representatives ... Trade, Distribution, Operations etc.) as well asother organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and Global Development… 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
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …ISO 14971, EU MDR/IVDR, China FDA, JGCP, ICH E6) + Knowledge and understanding of clinical development programs and clinical trial processes as well as ... best self. Become a **maker of possible** with us. The **Sr. Clinical Quality Specialist ** is responsible for supporting the Global Clinical Research… more
- Abbott (New York, NY)
- …maintaining relationships with key physicians and site-specific stakeholders to achieve clinical trial enrollment objectives. This individual will be ... treating structural heart disease. As the Senior Therapy Development Specialist , you'll have the chance to work closely within...therapy development. + Define strategies to drive enrollment at clinical trial sites within assigned territory to… more
- IQVIA (Bayonne, NJ)
- …variance analysis, unbilled/unearned and cash flow management, backlog forecasting, and clinical trial forecasting. * Knowledge of Peoplesoft Project. * ... Overview The person providing these services is involved in clinical out of pocket (OOP) planning from the concept...phase through execution and closeout and is responsible for clinical out of pocket cost forecasting and supporting budget… more
- Merck (Rahway, NJ)
- … Specialist will be responsible for: + Authoring scientifically valid clinical trial registration and results postings on www.ClinicalTrials.gov (United ... Specialist may occasionally prepare plain language (lay) summary trial results at a 6-8th grade reading level and...Familiarity with United States and/or European Union legislation for clinical trial registration and result disclosure. MW20… more
- Hackensack Meridian Health (Hackensack, NJ)
- … trials. + Responsible for editing, negotiating, and executing industry sponsored clinical trial contracts. + Provides professional consultation, advice, and ... of positive change. The fundamental mission of a **Contract Specialist ** is to facilitate and promote the research endeavors...staff and corporate sponsors regarding contracting issues such that clinical trial contracts will best meet legal… more
- Hackensack Meridian Health (Paramus, NJ)
- …audits, as well as ensuring ongoing compliance of study-related documentation throughout the clinical trial lifecycle for all assigned clinical trials. ... serve as a leader of positive change. The **Regulatory Specialist ** is responsible for ensuring compliance with Federal, State,...the Medicare Coverage Analysis, budget and contract for a clinical trial in order to initiate a… more
- Actalent (Hackensack, NJ)
- …awareness in clinical research through ongoing education. Requirements + 2+ years clinical trial regulatory experience + IRB and GCP experience + Maintaining ... Clinical Practice (GCP), and Institutional policies. The Regulatory Specialist will serve as a liaison to investigators, collaborating...components of clinical trial + Bachelors degree preferred Soft… more
- Actalent (Hackensack, NJ)
- …- Assist in developing procedures to ensure regulatory compliance. Hard Skills + Clinical trial regulatory experience + Dealing with IRB + Maintaining components ... Job Title: Regulatory Specialist Job Description The Regulatory Specialist ...Clinical Practice (GCP), and Institutional policies. The Regulatory Specialist will serve as a liaison to investigators, collaborating… more
- Weill Cornell Medical College (New York, NY)
- …for this role when Hired for NYC Offices **Position Summary** Oversees the clinical trial regulatory maintenance from study submission through closeout. **Job ... Title: Regulatory Specialist Location: Upper East Side Org Unit: Geriatrics...projects. Prepares and submits all necessary documents to the Clinical Science Evaluation Committee (CSEC), the Institutional Review Board… more
- Hackensack Meridian Health (Paramus, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** A day in the ... on each protocol and each patient participating in a clinical trial protocol in the clinical...+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist … more
- Pfizer (New York, NY)
- …inspection experience + Process and system management experience + Detailed knowledge of clinical trial processes and relationships required + Knowledge of GCP ... **The Root Cause Analysis Specialist will be responsible to:** + Lead the...This role will involve working with Vendor Quality and Clinical Quality colleagues. + Work with Vendor Quality and… more
- Vitalief (Newark, NJ)
- …leading site solutions partner focused on improving the value and contribution of clinical trial sites across the drug development lifecycle. We offer integrated ... Workforce Solutions (training and career pathing), and Site Networks that enhance clinical trials and improve patient outcomes. We are seeking a problem-solving,… more
- Mount Sinai Health System (New York, NY)
- …federal government officials and drug and device manufacturers. 11. For Contracts Negotiates clinical trial agreements and amendments on behalf of Mount Sinai ... field or equivalent combination of education and relevant experience. + Clinical trials negotiation training (MAGI, etc.) desirable. + Certified IRB Professional… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …amendments, IRB/IEC submissions and regulatory submissions * Accountable for timely clinical trial execution, reviewing adverse events, monitoring patient ... delivering genetic medicines for patients with serious diseases * You have specialist postgraduate clinical training and practice, and/or scientific research… more
- ThermoFisher Scientific (New York, NY)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... FSO, FSP, Government, etc.). Acts as a site processes specialist , ensuring that the trial is conducted...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more