- Merck & Co. (Rahway, NJ)
- …in quality management or business management is preferred.Prerequisites:Minimum of 6 years in clinical research including at least 2 years with developing and ... Accountability, Adaptability, Clinical Data Management, Clinical Development, Clinical Quality Management, Clinical Research , Clinical … more
- Merck & Co. (Rahway, NJ)
- …and key strategic engagements. This includes the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in...(eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data collection… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our ... pharmacy services, including: + Drug therapy design and monitoring , patient medication counseling, and participation in Collaborative Drug...+ Located at 1275 York Avenue + Reporting into: Manager , Oncology Clinical Pharmacy **Please submit a… more
- Parexel (Trenton, NJ)
- …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years ... (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study...relevant experience in clinical research site monitoring (preferably 2 years in… more
- Parexel (Trenton, NJ)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... delivery of the study. The CRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Trenton, NJ)
- …processing cycle + Provide input as necessary to Feasibility Studies, Data Monitoring Committees (DMCs), Clinical Endpoint Committees (CECs) + Provide medical ... + Perform review and summarization of literature citations including epidemiology background research + Provide safety content review of clinical protocols,… more
- Parexel (Trenton, NJ)
- …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and… more
- Parexel (Trenton, NJ)
- …work remotely. The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will ... randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents + Perform sample-size… more
- Edwards Lifesciences (Trenton, NJ)
- …subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good ... skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical...cardiology trials + Master's Degree in related field + Clinical research certification (ACRP or SoCRA … more
- Mount Sinai Health System (New York, NY)
- …in strategic research goals, and implements best practices in clinical trial management, monitoring , vendor oversight, data quality, and regulatory ... **Job Description** The ** Clinical Trial Manager ** provides leadership and...etc) required. Master's degree or equivalent advanced training in clinical research or project management preferred. +… more
- Mount Sinai Health System (New York, NY)
- … Manager II** will oversee the entire portfolio of Investigator-Initiated Clinical Trials (IICTs)/ Clinical Research Sponsor Collaboration (CRSC) within ... among multidisciplinary teams to meet project goals. The Project Manager II will work closely with investigators, research...overseeing comprehensive training programs for new staff within the clinical research teams. This role ensures that… more
- Taiho Oncology (Princeton, NJ)
- …transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager , Clinical Research Scientist, you will play a pivotal role ... of cancer research . Position Summary: The Senior Manager , Clinical Research Scientist has...execution of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting… more
- Parexel (Trenton, NJ)
- The Manager , Central Monitoring is accountable for centralized monitoring activities for global and/or complex trials, analytical data review of key risk ... data and presenting as an integral member of the Clinical Study team for clinical development studies....interpreted, reported and presented to the study teams. The Manager , Central Monitoring , will be responsible for… more
- AbbVie (New York, NY)
- …of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials. (CRA ... Description The CRA II advances AbbVie's pipeline by striving for excellence in clinical research , turning science into medicine for patients, and leveraging… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown, NJ **About the Job** Join the engine of Sanofi's mission - where deep ... the impossible into possible for millions. As the **Senior Clinical Research Director** (Senior CRD) within the...review of data within the scope of the Centralized monitoring , clinical and medical information for the… more
- Mount Sinai Health System (New York, NY)
- …data submission, workflows and specimen handling. * Under the supervision of the clinical research manager , the coordinator maintains procedures necessary ... of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists… more
- Vitalief (New Brunswick, NJ)
- …in New Brunswick, NJ. Job Responsibilities: + Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you will be responsible ... and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs...Minimum of 1 to 2 years of experience in Clinical Research as a Clinical … more
- Mount Sinai Health System (New York, NY)
- …of cancer as a disease process, cancer treatment modalities, and the process of conducting clinical research . The CPM will follow a caseload of patients in the ... **Job Description** The Clinical Program Manager is responsible for...This position will be primarily assigned to our Downtown Clinical Research Programs which operate at Mount… more
