Clinical science jobs in Sayreville, NJCreate job alerts

If you are physically/mentally ill or healthy, get paid to trial new treatments and medications. This is a great way to earn additional income, sometimes from the comfort of your home. Participation in clinical trials can be a very rewarding experience. Not only do you get free access to cutting-...

CROs) for outsourced study activities such as CRF design, database set-up activities, database specifications, data validation process, User Acceptance Testing, training of study site personnel in CRF completion, and data clarification processes Oversee data cleaning activities and ensures protoc...

CROs) for outsourced study activities such as CRF design, database set-up activities, database specifications, data validation process, User Acceptance Testing, training of study site personnel in CRF completion, and data clarification processes Oversee data cleaning activities and ensures protoc...

We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II assigned to Early Development trials (Phase I). ICON plc is a world-leading healthcare int...

Collaborates with cross-functional groups to develop standard and custom data reports for quality data oversight / clinical data review. ...

We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II. ICON plc is a world-leading healthcare intelligence and clinical research organization. C...

Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings. Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer d...

Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Have a m...

Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations and may prepare clinical trial budgets. Experience with Good Clinical Practice (...

Our client, a global pharmaceutical organization, has engaged GForce Life Sciences to provide them with a Clinical Programmer. This SAS programmer will support an ongoing and planned 2022 clinical trial analysis, reporting, and MAA submission. Bachelor’s degree in Statistics, Mathematics, or Comp...

MS in Statistics, Computer Science or a related field with + years of relevant experience. OR BS in Statistics, Computer Science or a related field with + years of relevant experience. ...

Job Title: Business Development Manager Life Sciences Clinical Platforms, NALocation: New Jersey, USAJob OverviewPrimary responsibility will be to sell Life Sciences Clinical Platforms subscriptions to large and mid-sized pharma and medical devices companies. This platform caters to end to end ne...

POST MARKETING-PRECLINICAL-PHASE OR LATER. ...

Solid understanding of clinical research methods, Clinical Data Interchange Standards Consortium (CDISC) principles, best data management practices and technologies related to clinical trials. Review clinical study protocols and provide comments if any. Master's degree or higher in science or rel...

May act, in concert with senior clinical personnel, as the company spokesperson regarding publication of clinical research findings. Responsible for the translation and implementation of (non-medical) scientific concepts into the study design and/or program across planning, execution, and reporti...

Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource planning, vendor oversight, EDC build and study timelines, etc. Develop and manage standard operation procedures (SOP and CLPs) for ...

We have a long-term, % remote contract opportunity for a life sciences Clinical Trials Business Analyst with Study Data Tabulation Model (SDTM) experience. Our client is currently seeking a Clinical Business Analyst to support a project involving SDTM generation. ...

Minimum years of experience in Clinical Data Management. ...

Collaborates with cross-functional groups to develop standard and custom data reports for quality data oversight / clinical data review. ...

TLF) shells, SDTM/ADaM specifications, clinical study reports, and other relevant documents. Experience with different clinical phases. Knowledge of clinical trial methodology and study design. ...

Archive clinical trial data (SDTM and ADaM datasets). Master's or degree in Statistics, Biostatistics, Epidemiology, and Computer Sciences. Clinical Trial Programming or years+ if Bachelor' Degree. ...

Responsible for the initiation and approval of the building, testing and validation of clinical databases, subsequent changes in clinical databases and data validation activities. Bachelor's degree in mathematics, Science or a related field, along with at least or more years of clinical data mana...

... clinical care and academic endeavors. In the department are 124 physicians and basic scientists who conduct collaborative research with an emphasis on mechanisms of disease, novel therapies ...

Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.