Clinical trials jobs

Hybrid in Foster City, California

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11d ago

About Nexinfo: NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challeng

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Contract

$60 - $70

Data Scientist

Remote or Hybrid in Novato, California

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Today

Data ScientistJob Summary: Talent Software Services is in search of a Data Scientist for a contract position in Novato, CA. The opportunity will be for three months with a strong chance for a long-term extension.Position Summary: Client's Data Science is responsible for designing, capturing, analyzing, and presenting data that can drive key decisions for Clinical Development, Medical Affairs, and other business areas of Client. With a quality-by-design culture, Data Science builds quality data t

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Contract

BASED ON EXPERIENCE

RN - HIV Medicine Practice

Albany, New York

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Today

Department/Unit: HBD - Aids Program Work Shift: Day (United States of America) Salary Range: $83,200.00 - $128,960.00 Salary range: $33/hr. - $47.60/hr. Registered Nurse (RN) ? Full Time HIV Medicine Clinic - Albany, NY We have an exciting part time opportunity for a caring and compassionate RN to join our HIV Medicine Clinic team of dedicated healthcare providers! The Albany Medical College Division of HIV Medicine (DHIVM) offers comprehensive HIV services including primary medical care, me

Full-time

Compensation information provided in the description

Data Scientist / ML Specialist (Pharma Domain) - Barcelona SPAIN

Barcelona, Catalonia

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23d ago

Essential Education & background o MSc or PhD in Statistics, Biostatistics, Data Science, Mathematics or related quantitative field. o Strong foundation in probability, statistical inference, and regression modelling. Technical skills o Proven experience with multivariate linear regression (incl. diagnostics, handling multicollinearity, transformations, interaction terms, model selection). o Hands-on experience with survival analysis, especially Cox proportional hazards models (assumption checki

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Full-time

$20 - $60

Clinical Study Administrator

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose fr

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Contract

eCOA Build Programmer

Remote

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11d ago

Handson experience as programmer in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementationDesign of electronic CRF screens to capture Clinical data and build on required validationsUnderstanding of Clinical Protocol and interpretation of the Clinical terminologies to create or design specificationsFamiliarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of systemAnalyse

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Full-time

$140,000 - $180,000

CLINICAL DATABASE DEVELOPER - Hybrid - Secret (preferred) or higher

Hybrid in Thurmont, Maryland

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4d ago

TheOffice of Regulated Activities (ORA)is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA providesfull-service, oversight,andconsultationfor regulatory, clinical, non-clinical, manufacturing, data management, biostatistics, product technical, safety monitoring.How a Clinical Database Developer will make an Imp

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Full-time

Depends on Experience

3rd party data acquisition Study Analyst

Boston, Massachusetts

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Today

Roles & Responsibilities: Serve as the subject matter expert for planning, setup, and acquisition of external clinical data at the study level, managing study startup, conduct, and closeout activities. Create external data transfer agreements, ensuring alignment with company standards and specifications to support data integration, analysis, and reporting. Provide guidance in setting up infrastructure for external data flow into company clinical data pipelines. Oversee the validation of all thir

Full-time

Senior Clinical Research Program Manager

Westbury, New York

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Today

Job Description Provides management of research administration at a clinical site(s) including monitoring the quality and accuracy of clinical trial data. Follows the established monitoring Standard Operating Procedures (SOP) and protocol- specific monitoring plan. Participates in site initiations and trainings. Job Responsibility 1.Trains, coaches, supports and mentors Site Clinical Research Managers and other team members. 2.Manages the clinical research sites including, but not limited to

Full-time

USD 66,220.00 - 108,180.00 per year

Clinical Study Assistant

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking a Clinical Study Assistant for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from.

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Contract

Medical Writer 2

Sunnyvale, California

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Yesterday

Primary Function of Position: This position reports to Manager, Medical Science and requires a strong candidate with experience in medical writing of clinical regulatory documents. The position will mainly focus supporting the inhouse team with the Clinical Evaluation Reports (CERs), with potential for future additional responsibility for development of other clinical evidence documents. The purpose of this job is to support clinical evaluation reports (CERs) per Medical Device Regulation (MDR

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Contract

$70

Clinical SAS Programmer

Newark, New York

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Today

Responsibilities: Engage directly with cross-functional teams and contribute to high-visibility clinical initiatives Work on-site in a collaborative setting that encourages knowledge sharing and technical excellence Lead programming efforts supporting clinical studies and regulatory deliverables Develop and validate SDTM and ADaM datasets in alignment with CDISC standards Produce high-quality analysis outputs, including tables, listings, and figures for trials and publications Create, maintain,

Full-time

Clinical SAS Programmer

Boston, Massachusetts

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Perfo

Full-time

Director of Data and Biostatistics (Only W2, No C2C)

Acton, Massachusetts

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Yesterday

Job Title: Director of Data and Biostatistics (Only W2, No C2C) Job Location: Acton, MA (Hybrid)Job ID: 407 Job Location: 12 Months Must be local to Acton, MA and available for onsite meetings Description: The Director of Data and Biostatistics will lead data operations for our Clinical Affairs team focused on medical devices. This role will be responsible for overseeing the design, implementation, and maintenance of clinical data systems, ensuring data integrity, and supporting regulatory co

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Contract

$130 - $145

Clinical SAS Programmer

Santa Clara, California

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Today

Responsibilities: The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures (TLFs) that support clinical trial reporting, regulatory submiss

Full-time

Clinical SAS Programmer

Omaha, Nebraska

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements Provides input in the design and development of case report forms and clinical databases Performs

Full-time

Senior Clinical Research Specialist

Remote or Irvine, California

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Today

Senior Clinical Research Specialist Kelly Science and Clinical FSP is currently seeking a Senior Clinical Research Specialist for a long-term engagement in Irvine, CA with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vison, 401K,

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Contract

Medical Director, Clinical Science - Solid Tumor

Boston, Massachusetts

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Today

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Medical Director, Clinical Scien

Full-time

USD 228,200.00 - 358,600.00 per year

Data Scientist II, O'Donnell Brain Institute

Dallas, Texas

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Today

WHY UT SOUTHWESTERN? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report , we invest in you with opportunities for career growth and development to align with your future go

Full-time

Senior Medical Director, Clinical Science -Solid Tumor

Boston, Massachusetts

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Today

Full-time

USD 257,600.00 - 404,800.00 per year

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Clinical trials jobs