- 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
- 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
- Boehringer Ingelheim (Ridgefield, CT)
- … clinical programs across Therapeutic areas, ie, Clinical Associates (CAs), Clinical Trial Operations Specialist (CTOS), Regulatory Start Up ... for forecasting and providing oversight of resources supporting US Clinical Trial Managers (CTMs)and managing the Site...Specialist (RSUS), Informed Consent Specialist (ICS) Site Activation Manager (SAM), Establishes standards. This… more
- Boehringer Ingelheim (Ridgefield, CT)
- …to work on one or more clinical trials under the supervision of an experienced Clinical Trial Manager (CTM) and/or Clinical Trial Leader (CTL). The ... + Select sites for study conduct and deliver the trial according to the clinical trial...CRAs, investigators and site staff + In collaboration with Trial Resource Specialist and with support from… 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
- Weill Cornell Medical College (New York, NY)
- …and coordinates site initiation visits, regulatory monitoring visits, and assists with clinical trial audits or inspections. + Maintains and disseminates ... Title: Regulatory Specialist -CCTO Location: Lower East Side Org Unit: Regulatory...Summary** Under general direction, oversees the regulatory aspects of clinical trials from start-up through study closeout. **Job Responsibilities**… more
- Lilly (Stamford, CT)
- …be accountable for compliance of team members. + Lead completion of clinical trial documents including protocols, amendments, investigator brochures, informed ... input for site selection, investigator meetings, steering committees, and clinical trial training. + Participate in data...graduate degree such as, PharmD, PhD, MSN with advanced clinical specialty ( Clinical Nurse Specialist /Nurse… more
- Veterans Affairs, Veterans Health Administration (New York, NY)
- …complete review of the EDRP application. Responsibilities Major Duties Include - Clinical Laboratory Scientist works throughout the lab as a generalist and works ... will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness...given by ASCP BOR or AMT. Categorical certification or Specialist certification by ASCP or AMT. May qualify based… more
- Hackensack Meridian Health (Hackensack, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Education, Knowledge, Skills and ... field. + Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the… more
- Pfizer (New York, NY)
- …deliverables including SCE and SCS + Support appropriate interpretation and communication of clinical trial data. + Review and approve submission level safety ... opportunities in support of the Obesity portfolio. This may include responsibilities for trial design, execution and reporting of clinical trials for other… more
- Boehringer Ingelheim (Ridgefield, CT)
- …under their responsibility as delegated by TA HoEM. + Review and approve final Clinical Trial Reports, Clinical Trial Protocols, scientific publications ... + Ensures the review of the Master Plans, related Clinical Development plans and Clinical Trial...(IND enabling activities through Proof of Concept studies), ideally clinical specialization hematology, oncology or organ specialist .… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Evidence needs is defined and the optimal source of evidence defined (Randomized Clinical Trial , Real-World Evidence, Market Research and others). + Brings the ... Profile is validated with external experts and reflects patient's needs and inform Clinical Trial Protocols). This includes services and solutions beyond the… more
- Boehringer Ingelheim (Ridgefield, CT)
- …all relevant internal global functions (eg Epidemiology, early and late-stage Clinical Development teams, Regulatory Affairs, Drug Safety, Marketing, PPSS (Product ... + In collaboration with the matrix team, plans for phase IV trial program and non-interventional studies; where applicable coordinates and provides guidance for… more
- Edwards Lifesciences (New York, NY)
- …+ Nurse Practitioner or Physician Assistant in structural heart + Experience as a Clinical Specialist , Therapy Development Specialist , Clinical Education ... you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality… more
- Weill Cornell Medical College (New York, NY)
- …MCC CCTO representative, in the absence of the Research Nurse Administrator. Serve as clinical trial operations expert in clinical research policies and ... Nurse Administrator assists with the day-to-day management of the Research Nurse Specialist and Medical Assistant. **Job Responsibilities** + Serves as a resource to… more
- BMO Financial Group (New York, NY)
- …for covered companies, including ratings and target prices + Ability to analyze clinical trial design and data across early and late-stage oncology trials ... external stakeholders. The ideal candidate can translate scientific analysis and clinical data into differentiated and actionable investment theses for buy-side… more