Clinical trials jobs

Hybrid in Foster City, California

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5d 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

Research And Development Technician

Miramar, Florida

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13d ago

We are looking for Research And Development Technician for our client in Miramar, FL Job Title: Research And Development Technician Job Location: Miramar, FL Job Type: Contract Job Description: Essential Functions: Performs conduct procedures in strict compliance to the study protocol, Good Clinical.Practice standards, Standard Operating Procedures (SOP's), QA/QC procedures, OSH guidelines and other state and local regulations as applicable.Provides assistance in the execution of clinical trial

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Contract, Third Party

Depends on Experience

Senior AI Architect

Jersey City, New Jersey

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20d ago

Senior AI Architect Location: NJ Fulltime Key Responsibilities Design, build, and deploy robust ML/AI models for applications in drug discovery, clinical trials, bioinformatics, or operational excellence. Develop and maintain scalable data pipelines for processing large volumes of structured and unstructured scientific and clinical data. Collaborate with data scientists and domain experts to translate scientific problems into machine learning solutions. Evaluate and implement state-of-the-art

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Full-time

150,000 - 200,000

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

Clinical Research Leader (Hybrid) (No C2C or H1B)

Irvine, California

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4d ago

Please note that this position is a long-term contract role with benefits. This position is a hybrid role - onsite Tuesday and Thursday and every other week Friday onsite. Position requires 15% of travel with plenty of notice prior to travel. EXPERIENCE AND EDUCATION - Minimum of a Bachelor's Degree, preferably in Life Science, Physical Science, Nursing, or Biological Science, required. - BS with at least 6 years, MS with at least 5 years, PhD with at least 3 years of relevant experience preferr

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Contract

Depends on Experience

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

Barcelona, Catalonia

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17d 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

eCOA Build Programmer

Remote

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5d 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

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

Associate Director, Biostatistics

King of Prussia, Pennsylvania

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Today

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Main Responsibilities: Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical

Full-time

Associate Director, Biostatistics

King of Prussia, Pennsylvania

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Today

Full-time

Medical Writer 2

Sunnyvale, California

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6d ago

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

Clinical SAS Programmer

Baltimore, Maryland

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Today

Responsibilities: Perform data manipulation, analysis and reporting of primarily clinical trial data. Create SDTM data sets. Create analysis data sets. Program and generate tables, listings and graphs (TLGs). Validate and document SAS programs and output. Fulfil ad-hoc analysis requests. Other services as needed. Requirements: Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or related applicable field. Minimum of 5 to 8 ye

Full-time

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

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

Acton, Massachusetts

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2d ago

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

Principal Biostatistician

King of Prussia, Pennsylvania

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Today

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Principal Biostatistician? The job is in our King of Prussia, PA, Waltham MA and Maidenhead UK office. This is a hybrid

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

Clinical SAS Programmer

Dallas, Texas

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Today

Responsibilities: Develop and maintain SAS programs to import, clean, and validate clinical trial data. Use R for data manipulation, analysis, and visualization. Perform statistical analyses in accordance with study protocols and analysis plans. Generate tables, listings, and figures (TLFs) using SAS and R. Create and QC statistical outputs and clinical study reports for regulatory submissions. Document programming activities and ensure compliance with Standard Operating Procedures (SOPs). Work

Full-time

Clinical Lead Specialist, Structural Heart, TAVI (Sacramento / San Francisco / Seattle)

San Francisco, California

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Today

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life

Full-time

Compensation information provided in the description

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Clinical trials jobs