Clinical trials jobs

Project Manager Clinical Trials / CRO / Pharma (Remote - EST Hrs)

Remote

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2d ago

Project Manager Clinical Trials / CRO / Pharma (Remote - EST Hrs) We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the pharmaceutical Industry. This is a Remote position. Job Summary We are seeking an experienced Project Manager with a background in clinical trials, CRO operations, and pharmaceutical programs. The ideal candidate will manage cross-functional teams, support product-related initiatives, and ensure successful execution

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Contract

$60

Clinical Research Associate 3

Sunnyvale, California

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Today

Job Description Primary Function of the Position The Senior Clinical Research Associate will play a vital role in supporting pre-market clinical studies of investigational drugs for the Fluorescence Imaging group, ensuring full compliance with regulatory requirements. The ideal candidate will have in-depth knowledge of clinical research in drug trials, including Good Clinical Practice (Google Cloud Platform) and relevant US regulations for human subjects. As a member of the Clinical Fluorescence

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Third Party, Contract

$92

Medical Writer II

Hybrid in Sunnyvale, California

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7d ago

Job Title: Medical Writer II Location: Sunnyvale, CA 94043 (Hybrid) Weekly work hours: 30 Pay Rate: $70 on W2 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.

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Contract

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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Today

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

Senior Field Clinical Specialist - Central (WI, IL, KY)

Green Oaks, Illinois

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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. Job Title Senior Field Clinical Specialist Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your f

Full-time

Compensation information provided in the description

SAS Programmer

Atlanta, Georgia

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Today

Responsibilities: The statistical programming contractor independently manages completed projects that involve global tasks, or cross functional teams. The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G In addition, providing programming support for publication for our marketed drugs Primarily works at the study, product / program level. Provides comprehensive programming support, including deve

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

SAS Programmer

Omaha, Nebraska

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Today

Roles & Responsibilities: 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 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. Create source and validation programs using SAS software for SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products. Integrates data across

Full-time

Manager Research Integrity

Kent, Ohio

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Today

Full-time, 40 Hours/Week Monday to Friday, 8am - 5pm Hybrid (Onsite 2-3 days/week) Summary: The Manager, Office of Research Integrity oversees the daily operations of the Office of Research Integrity, ensuring alignment with institutional goals and compliance with internal and external regulations. This role collaborates closely with Research Administration, Legal Services, and Compliance to support research integrity across the organization. The manager supervises staff and functions related t

Full-time

Manager Research Integrity

Brecksville, Ohio

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Today

Full-time

Manager Research Integrity

Akron, Ohio

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Today

Full-time

Manager Research Integrity

Cleveland, Ohio

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Today

Full-time

Manager Research Integrity

Doylestown, Ohio

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Today

Full-time

Engineer II

Gainesville, Florida

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Today

Engineer II Job no: 537931 Work type: Staff Full-Time Location: Main Campus (Gainesville, FL) Categories: Engineering, Physical/Mathematical Sciences Department:27280202 - HA-MBI AMRIS Classification Title: Engineer II Classification Minimum Requirements A high school diploma or equivalent and six years of relevant experience; appropriate college coursework or vocational/technical training may substitute at an equivalent rate for the required experience; or Bachelor's degree in an appropr

Full-time

USD 61,000.00 - 70,000.00 per year

Medical Writer 2

Sunnyvale, California

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Today

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, Third Party

$70

Clinical SAS Programmer

Austin, Texas

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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

Tarrytown, New York

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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.

Full-time

Clinical SAS Programmer

Irvine, California

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Today

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement progra

Full-time

Associate Clinical Site Lead - Northern California

Pleasanton, 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. Summary Under the supervision of senior colleague/manager (or delegate), the Associate Clinical Site Lead drives study execution and operational exce

Full-time

Compensation information provided in the description

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Clinical trials jobs