Trabajos clinical science en Livingston, New Jersey (NJ) State

Our individualized treatment is supported by clinical research and translational science. License/Certification: • DEA Certification (Preferred) • Certified Nurse Practitioner (Required) • ...

As New Jerseys only National Cancer Institute (NCI) designated Comprehensive Cancer Center, Rutgers ... of research discoveries in basic, clinical, and population science as well as the ability to ...

Functional Area DescriptionThe Clinical Scientist Team Lead reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. DMC) activitiesClinical contributions to clinical study reports (CSRs) and clinical portions...

BS/MS in Statistics, Biostatistics, Computer Science, Mathematics or Life Sciences. Clinical Programmer, Consultant. Experience with all clinical phases I, II, III and IV of trails is desirable. Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA, WHODRUG...

Functional Area DescriptionThe Clinical Scientist Team Lead reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. DMC) activitiesClinical contributions to clinical study reports (CSRs) and clinical portions...

This role is a member of the Clinical Records leadership team to ensure optimum implementation of the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program. The Associate Director, Clinical Records & Inf...

BA / BS computer science/information technology or life sciences from a year accredited university. Designs and creates clinical databases. Minimum years clinical database programming experience preferred in the device / pharmaceutical / CRO industry. Experience with development, validation, exec...

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...

Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products. C...

Develop and maintain global clinical data standards, including operational (eCRF and external), post-process, Study Data Tabulation Model (SDTM), controlled terminology, external data mappings (, lab or ECG), and other applicable standards. Act as an expert on operational data standards, SDTM and...

In partnership with Clinical Research, Medical Affairs and Development functions, ensures that all clinical trial activities are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global ...

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...

Adequate knowledge in clinical trial research methodology, ICH, GCP and regulations. ...

Clinical operations representative on early development teams (EDT) and/or oversees direct reports serving on EDTs, ensuring clinical operations strategic and operational input to clinical development programs. Strong collaboration and partnership with cross functional colleagues globally (Clinic...

Clinical operations representative on early development teams (EDT) and/or oversees direct reports serving on EDTs, ensuring clinical operations strategic and operational input to clinical development programs. Strong collaboration and partnership with cross functional colleagues globally (Clinic...

Clinical Trials Manager, Clinical Operations - Oncology (CTM). We are seeking a talented, experienced, and highly motivated candidate to join the Oncology Clinical Operations team. Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monit...

Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products. C...

Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products. C...

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation...

Master's degree in health economics and outcomes research, statistics, mathematics, psychology, epidemiology, computer science, or related fields. Demonstrate knowledge of real-world evidence (RWE) databases and clinical trial data. Apply various statistical methods to real-world research and cli...

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...

Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products. C...

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Undergraduate degree or international equivalent in clinical, science, or health-related field from an accredited institution; health c...

... Clinical Trial Application (CTA) queries on new protocols and protocol amendments in compliance with HA deadlines. Degree Requirements Solid scientific background, Ph.D., M.D., PharmD, MS, or BS ...