- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and immune disorders. Summary This position supports the strategy for driving global Clinical Study Start -Up activities for PV Safety Operations. This ... clinical study safety reporting and activities.Global Clinical Study Start -Up Documentation: Reviews... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to ... Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction with key… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the TMF document… more
- Merck & Co. (Rahway, NJ)
- …for the execution of the Merck clinical research portfolio. The Clinical Sciences & Study Management Department of the GCTO organization focuses on the ... for a single study or across multiple studies (eg, operational deliverables, clinical & ancillary...intends to: Develop an understanding of the phases of clinical research . Develop an understanding of the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …assigned clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and review Statistical Analysis Plans (SAPs) and statistical ... Summary This position supports proactive safety surveillance and risk management for assigned clinical studies in partnership with Clinical Safety Scientist… more
- Merck & Co. (Rahway, NJ)
- …for the execution of the Merck clinical research portfolio. The Clinical Sciences & Study Management Department of the GCTO organization focuses on the ... study team with the scientific conduct of clinical studies . In this position, you will...intends to: Develop an understanding of the phases of clinical research . Develop an understanding of the… more
- Merck & Co. (Rahway, NJ)
- …in 47 countries, responsible and accountable for the execution of the Merck clinical research portfolio. The Global Clinical Operations (GDO) department ... study sites, vendors, committees, etc.) in support of clinical study objectives.--You will be part of...intends to:- Develop an understanding of the phases of clinical research -- Develop an understanding of the… more
- Merck & Co. (Rahway, NJ)
- …curious, join us-and start making your impact today.--Overview:-- -Merck Research Lab's (MRL) Pharmaceutical Sciences & Clinical Supplies (PSCS) organization ... Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company Research Laboratories portfolio… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …or indirectly support Feasibility and/or additional related areas (eg study start up, protocol development) to ensure Global Clinical Operations (GCO) goals ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....reaches out and build relationship with key program and study staff at clinical development and operational… more
- Kelly Services (New York, NY)
- ** Clinical Research Study Start Up Manager** **Position: Clinical Research Start -Up Manager - Hybrid** **Job description** : The Clinical ... research network based out of Brooklyn, New York with an immediate need for a Clinical Research Start Up Manager for their clinical trials. As part of… more
- Merck (Rahway, NJ)
- …for the execution of the Merck clinical research portfolio. The Clinical Sciences & Study Management Department of the GCTO organization focuses on the ... for a single study or across multiple studies (eg, operational deliverables, clinical & ancillary...to: . Develop an understanding of the phases of clinical research . . Develop an understanding of… more
- Vitalief (New Brunswick, NJ)
- …departments as needed. + Facilitates clinical trial billing administrative start -up, insuring clinical research billing and regulatory compliance. ... beginning of protocol submission to the end of the study utilizing OnCore CTMS system. + Performs regular audits... of financial data and transactions. + Experience in clinical research administration; knowledge of regulatory, financial… more
- The Mount Sinai Health System (New York, NY)
- …to assist in the daily activities of clinical research studies , including collection and organization of study information. Assists in preparing grant ... Advancing medicine. Healing made personal._** **_Roles & Responsibilities:_** The ** Clinical Research Coordinator (CRC)** at the **Alzheimer's...at Icahn School of Medicine at Mount Sinai, assists clinical studies sponsored by the NIH and… more
- HSS (New York, NY)
- …Previously worked with industry sponsored/funded studies (specifically independent execution of study start up to close out) + Previous management experience ... can be part of our transformation across the enterprise. Clinical Research Manager - Industry Full-Time Summary:...will be responsible for submitting all visits required for study milestones (eg start -up/initiation, quality & audit… more
- Vitalief (New Brunswick, NJ)
- …is 100% on-site in New Brunswick, NJ Responsibilities: + Under the direction of the Clinical Research Study Site Leader, this resource will be responsible ... new clinical trial protocols assigned utilizing Oncore Study - start up task list. + Collaborate with...start up task list. + Collaborate with the clinical research team to ensure timely prescreening… more
- IQVIA (New York, NY)
- IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- Actalent (New York, NY)
- …Data verification + Data management Qualifications: + Minimum of three years in a Study Coordinator or Clinical Research Coordinator role + Oncology ... Clinical Research Coordinator *This is a...act as one of the main CRC's for this study . Please note, as the position and study...normal business hours Hourly pay range: $30-33 per hour Start date: 2-3 weeks About Actalent Actalent is a… more
- New York University (New York, NY)
- …of contact to the principal investigator, study sponsor and IRB for multiple research studies . Candidate will be responsible for coordinating all aspects of ... of CRFs, recruitment strategies, IRB submissions, informed consent process, collecting clinical research data and maintaining accurate regulatory binders and… more
- Merck (Rahway, NJ)
- …for the execution of the Merck clinical research portfolio. The Clinical Sciences & Study Management Department of the GCTO organization focuses on the ... study team with the scientific conduct of clinical studies . In this position, you will...to: . Develop an understanding of the phases of clinical research . . Develop an understanding of… more
- Merck (Rahway, NJ)
- …Description** This position drives scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the Program Lead, you will ... collaborate with global, cross- functional team members including clinical directors and study managers to lead/support...+ Participates in the set up and design during study start up (eg, database set up)… more
