- Medtronic (New York, NY)
- **Careers That Change Lives** In this exciting role as a Principal Field Clinical Specialist , you will provide day-to-day field clinical study support, ... years of clinical support ( _e.g., field clinical specialist / clinical engineer or relevant...Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials + Proficient in MS Office… more
- Actalent (Basking Ridge, NJ)
- Job Title: Clinical Trials SpecialistJob Description Our Clinical Trials Specialist will play a key role in supporting Clinical Study Leads with ... the execution of global clinical trials . This includes both internally sourced studies and those...will track site activation, monitor updates, and assist with clinical trial registry postings. The role also… more
- Rockefeller University (New York, NY)
- …and new investigator audits, tracks deviations for early intervention, and supports clinical trial registration in Good Clinical Practice (GCP) ... For more information,please see the hospital website at: http://www.rucares.org/ Overview The Clinical Research Specialist serves as a regulatory expert and… more
- Vitalief (Newark, NJ)
- …is an innovative Healthcare consulting company, focused on empowering Research and transforming Clinical Trials . As a result, we are seeking a talented and ... enthusiastic Clinical Pharmacist Specialist to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our… more
- Merck (Rahway, NJ)
- …stakeholders including the Global Project Manager, Alliance Manager, Global Trial Manager, Clinical Sub Team, Clinical Trial Team, Outsourced Trial ... **Job Description** **Position Description:** **Senior Specialist , Oncology Clinical Development Finance** Under the guidance of the Oncology Clinical … 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)
- …full our company's Research Laboratories (Research and Development Division) portfolio of clinical trials . GCS is accountable for the planning, sourcing, ... serves as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent is… more
- Merck (Rahway, NJ)
- … supply chain across the full company's Research Laboratories (MRL) portfolio of clinical trials . GCS is accountable for the planning, sourcing, labelling, ... include, but are not limited to:** + Participates on the Clinical Trial Team(CTT)and collaborates closely with other functional area representatives to negotiate… 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
- Kelly Services (Bridgewater, NJ)
- …* Ensure compliance with regulations, all SOPs and partner agreements. * Review of Clinical trial protocols Phase I Phase III to ensure consistent and proper ... letters for IND Safety reports generated from company sponsored clinical trials . * Analyze metrics for critical...and post-marketed safety data; recommend changes to labelling and Clinical Trial Investigator Brochure as needed. *… 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
- Abbott (Hoboken, NJ)
- …heart arrhythmias, or irregular heartbeats. **WHAT YOU'LL DO:** The Regional Leadless Specialist provides technical, clinical , educational and sales support to ... ensure adoption and growth of Abbott leadless technology. The Regional Leadless Specialist works closely with internal and external customers to drive therapy… 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
- 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 (Paramus, 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
- Merck (Rahway, NJ)
- …GDO focuses on data collection, data review and integrity throughout the lifecycle of clinical trials . Clinical trials provide the required data ... a diverse, cross-functional team of individuals who execute our clinical trials . The Fellowship will include progressive...tools critical to the oversight and conduct of a clinical trial . Participate in team meetings… more
- Hackensack Meridian Health (Hackensack, NJ)
- …**Research Billing Compliance Specialist ** reviews, adjusts, and reports on clinical trials charges and claims representing research while working closely ... for ensuring research charges are posted in accordance with Medicare's Clinical Trial Policy, federal regulations and pharmaceutical/third party contracts.… more
- Merck (Rahway, NJ)
- …Department of the GCTO organization focuses on the planning, execution and close out of clinical trials within a program. Clinical trials provide the ... the scientific planning and execution of one or more clinical trials . You will assist the Lead...tools critical to the oversight and conduct of a clinical trial . . Participate in team meetings… more
- IQVIA (Parsippany, NJ)
- …in the development of safe, efficient, and effective investigational product (IP) preparation in clinical trials . The PIPS will be the key internal and external ... **Job Summary:** The Pharmacy Investigational Product Specialist (PIPS) will serve as a subject matter...intravenous, subcutaneous, and intramuscular. * Experience in the (virtual) clinical trial setting. * Experience in working… more
- Actalent (Hackensack, NJ)
- …Description The Research Compliance Specialist reviews, adjusts, and reports on clinical trials charges and claims representing research. This role involves ... that research charges are accurately posted in compliance with Medicare's Clinical Trial Policy, federal regulations, and pharmaceutical/third party contracts.… more