Clinical science jobs in Piscataway, New Jersey (NJ) State

Position Status Full Time Posting Number 24FA0341 Posting Open Date 03/04/2024 Posting Close Date Qualifications Minimum Education and Experience The successful candidate is expected to:• Have a doctorate in clinical psychology or related social science field• Have an established, active program ...

Working with the Asset Development Team (ADT's), early- & late-stage clinical development teams, the Biomarker (BMx) leads will develop asset-specific clinical biomarker strategy by incorporating critical insight from discovery biology, clinical development, diagnostics, bioinformatics, molecular...

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...

The Clinical Project Scientist is responsible for the design, planning, implementation, monitoring, and reporting of clinical research trials. Serves as liaison to global clinical sites for medical questions related to the clinical research trial ;. Clinical Project Scientist (Oncology). Partners...

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...

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 trials including knowledge of applicable clinical research regulatory requirements; , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. BA/BS in computer science, statistics, computer science, or public health with at least years performing stat...

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...

Clinical Data Management + years' experience across Phase - clinical trials. Performs coding review for adverse events, medical history and concomitant medications and coordinate medical monitor review and approval of medical coding with the clinical study manager and Medical Monitor. Supports cl...

For more than onehundred years, L’Oréal believes that beauty needs Science. Science & Technology are allowing us to invent safe, trustable,sustainable & responsible beauty products and experiences that will changepeople’s lives. As a Scientist in our Photoprotection Clinical andInstrumental Evalu...

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...

Position Title: Senior Clinical ScientistI, Skin Clinical & Physics (Instrumental) Sciences, Evaluation Intelligence. We are seekinga Senior Scientist I with aninnovative mindset to join our SkinClinical and Physics (Instrumental) Sciences Evaluation Intelligence Teamin our Clark, New Jersey rese...

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...

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 (...

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...

Degree in life science, computer science, business administration or related field. Lead electronic submission activities and assist with response to questions and findings from Clinical Quality Assurance (Quality Assurance) and other audits at the study / vendor level. Doctorate Degree OR Master...

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...

Culture primary cells and continuous cell lines such as neutrophils, hematopoietic stem cells, immune cells, and/or relevant cell lines to support in vitro/ex vivo experiments.Perform in vitro assays including various compounds screening assays and enzymatic assays.Conduct molecular biology techn...

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...

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...

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...

Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center. The company provides 24×7 delivery globally, with teams across the world's 3 ...

Global Life Science Hub is proud to partner with a specialised Biopharmaceutical company leading ... Ensure the timely execution of engineering and clinical batches. * Develop equipment specifications ...