- Merck & Co. (Rahway, NJ)
- … database design and development activities supporting startup of a clinical trial .Activities supported may include standards technical component development ... and the design and implementation of the clinical study database.Reviews technical feasibility of proposed forms, edit...capabilities used for review, cleaning and verification activities of clinical data captured in clinical trials and… more
- Merck & Co. (Rahway, NJ)
- …understanding of the systems and tools critical to the oversight and conduct of a clinical trial - Participate in team meetings to develop an understanding of the ... different skills and expertise of data management within a clinical trial team-- - Benefits of Fellowship...Transition Opportunities: This Fellowship will be geared towards a Specialist position and aligns to a full time transition… more
- Merck & Co. (Rahway, NJ)
- …understanding of the systems and tools critical to the oversight and conduct of a clinical trial . Participate in team meetings to develop an understanding of the ... and expertise of the cross functional members of a clinical trial team. -Benefits of Fellowship Mentoring...Transition Opportunities: This Fellowship will be geared towards a Specialist position and aligns to a full time transition… 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...Specialist may occasionally prepare plain language (lay) summary trial results at a 6-8th grade reading level and… more
- Merck & Co. (Rahway, NJ)
- …internal and external stakeholders (eg, study team, vendors, committees) in support of clinical trial objectives. You will be part of a diverse, cross-functional ... tools critical to the oversight and conduct of a clinical trial . Participate in team meetings to...Transition Opportunities: This Fellowship will be geared towards a Specialist position and aligns to a full time transition… 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 ... with Rutgers University and seeking several talented and enthusiastic Clinical Trial Recruitment Specialists to join our...areas that are underrepresented in research. As a recruitment specialist , you will play a vital part in these… 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
- Actalent (Basking Ridge, NJ)
- …! This company has great culture and is rapidly growing! Summary: The Clinical Trial Specialist /In-house CRA provides technical and administrative support ... 3 IMMEDIATE CLINICAL TRIALS SPECIALIST OPPORTUNITIES IN ONCOLOGY...to the clinical study team(s) responsible for clinical trial execution. This person may be… 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
- 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
- Actalent (Basking Ridge, NJ)
- …at least 6-8 years of experience in clinical research. + Experience in clinical protocol and trial document development. + Solid knowledge of Good ... Job Title: Clinical Research Manager We have openings for a Project Manager, Clinical Operations with the largest, most comprehensive and integrated health care… more
- Merck (Rahway, NJ)
- … clinical database design and development activities supporting startup of a clinical trial . + Activities supported may include standards technical component ... development and the design and implementation of the clinical study database. + Reviews technical feasibility of proposed...capabilities used for review, cleaning and verification activities of clinical data captured in clinical trials and… 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
- System One (Plainsboro, NJ)
- …quality, performance, regulatory compliance, and patient safety related to managing assigned clinical trial sites and document handling. + Attends and ... the main goal. They are seeking a Senior Retention Specialist to support patients enrolled in the clinical... trials. + A minimum of 5 years of clinical trial experience within a pharmaceutical, biotechnology,… more
- Actalent (Hackensack, NJ)
- … clinical staff, PFS, registration and third parties to ensure adherence to clinical trial billing workflows. + Provide guidance and serve as a resource ... for clinical trial regulations and best practices to...global functioning details. POSITION OVERVIEW: + The Research Compliance Specialist reviews, adjusts, and reports on clinical … more
- Hackensack Meridian Health (Hackensack, NJ)
- …for ensuring research charges are posted in accordance with Medicare's Clinical Trial Policy, federal regulations and pharmaceutical/third party contracts. ... a leader of positive change. The **Research Billing Compliance Specialist ** reviews, adjusts, and reports on clinical ...PFS, registration and third parties to ensure adherence to clinical trial billing workflows. + Provides guidance… more
- Medtronic (New Brunswick, 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 (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
- Northwell Health (Lake Success, NY)
- …meetings This position primarily reviews complex medical oncology histories for clinical trial eligibility and professionally communicates eligibility criteria, ... collaborating with members of the research team to provide an efficient clinical trial enrollment process for the patient, maintaining a waitlist of referred… more
