clinical trials Jobs

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Clinical Operations Lead

Cosmic-I LLC DBA Northern Base

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Mississauga, Ontario, Canada

Contract

About the Role: As a Clinical Operations Lead, you will play a pivotal role in the successful execution of clinical studies within Canada. You will be responsible for the end-to-end management of study activities, from initial site start-up, ongoing study conduct and close-out ensuring data quality and regulatory compliance. This highly impactful role requires a deep understanding of local regulations, strong leadership skills, and a collaborative mindset to drive timely and high-quality study
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Posted 6 days ago | Updated 5 hours ago

Clinical Associate Consultant

Avance Consulting

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Richardson, Texas, USA

Full-time

Job Title:- Clinical Associate ConsultantLocations:- Indianapolis, IN/ Raleigh, NC/ Hartford, CT/ Richardson, TX/ Tempe, AZRequired Qualifications:At least 2 Years of experience in information technology.Experience and detailed understanding of Products like Veeva.End-end Clinical trial management process and related applications.Experience/knowledge on clinical reporting (internal, FDA) during study start to closeout phases.Experience/knowledge in Computer systems Validation activitiesFamiliari
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Posted 1 day ago

Senior Biostatistician

Radiant System, Inc

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Remote

Contract

Role: Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program.Will closely collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissionsWill report to a franchise team leader, within the Biostatistics and Statistical Modelling organisationWill carry out functional responsibilities in accordance with
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Posted 12 days ago | Updated 1 day ago

Lead Clinical Research Coordinator - Onsite

Nicklaus Children's Hospital

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Miami, Florida, USA

Full-time

Description Job Summary Under direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children's Research Institute. Ensures processes are in place and roles are defined in order fo
Posted 1 day ago | Updated 9 hours ago

Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLC

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Remote

Contract

Job Title: Sr. Principal StatisticsLocation: Remote Duration: 6 MonthsEmployment Type: W2 ContractExperience Level: Mid-SeniorEducation Required: Ph.D. or MS in Statistics or BiostatisticsIndustry: Pharmaceuticals Job Summary:The Sr. Principal Statistician will lead statistical activities in clinical trials, from protocol development to final study reporting. The role will also contribute to regulatory filings, in-licensing evaluations, and marketing support. Key Responsibilities:Review protocol
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Posted 21 days ago

Labware LIMS Specialist

Quantum World Technologies Inc.

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Kent, Connecticut, USA

Full-time, Contract, Third Party

Be Labware certified Strong Concepts of LIMS LabWare V6 V7V8 Detailed knowledge on Labware LIMS Architecture Labware Database Structures SAP Crystal Reports Oracle PLSQL Experience on implementing top tier LabWare LIMS implementation Hands on Experience in LIMS application development LIMS basic Language Subroutines Interfacing Upgrade and validation Experience in Labware Modules like LIMS Stability EM Inventory Storage Location Management Instrument Interfaces Lot Sample Management for Cli
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Posted 5 days ago | Updated 3 hours ago

Pharmaceutical Engineer

Afton Scientific

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Charlottesville, Virginia, USA

Full-time

Pharmaceutical Engineer Providing reliable pharmaceutical services and lasting relationships within the industry for over 30 years. Afton Scientific is a contract development and manufacturing organization (CDMO) in Virginia that specializes in small-batch filling of injectables from clinical trials to approved commercial drugs. Utilizing 35,000 Sq. Ft of manufacturing, lab, warehouse, and administrative space, Afton provides custom, innovative solutions for clinical to commercial sterile man
Posted 34 days ago | Updated 8 hours ago

Statistical Programmer

Georgia IT

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Remote

Contract

Job Title: Statistical Programmer Location: Remote Key Responsibilities Develop, validate, and maintain SAS programs for statistical analysis, regulatory submission, and reporting deliverables. Create analysis datasets (ADaM) and tables, listings, and figures (TLFs) for clinical trial data analysis. Collaborate with statisticians and data managers to define specifications for datasets and statistical outputs. Ensure compliance with CDISC standards, internal SOPs, and regulatory guidelines (FDA,
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Posted 4 days ago

Global IT Compliance Sr Specialist

Thermo Fisher Scientific

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Pennsylvania, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing so
Posted 16 days ago | Updated 10 hours ago

RN - HIV Medicine Office

Albany Medical Center

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Albany, New York, USA

Full-time

Job DescriptionDepartment/Unit: HBD - Aids Program Work Shift: Day (United States of America) Salary Range: $60,028.00 - $99,023.00 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, medical case management,
Posted 49 days ago | Updated 10 hours ago

Senior Manager, Global Agile Communications

Johnson & Johnson

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Remote or Raritan, New Jersey, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m
Posted 2 days ago | Updated 10 hours ago

Principal, Electronic Data Capture Developer

Takeda pharmaceutical

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Massachusetts, USA

Full-time

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 Privacy Notice and Terms of Use. 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 Princip
Posted 11 days ago | Updated 10 hours ago

Development Engineer (R2-R3)

Eli Lilly and Company

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Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined
Posted 44 days ago | Updated 10 hours ago

Engineering Documentation Expert- Medical industry

DBSI Services

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Fort Worth, Texas, USA

Full-time

Job Title: Engineering Documentation Expert- Medical industry Location: Fort Worth, TX Bachelor's or master's degree in mechanical Engg. with 10+ years of clinical trials experience Engineering documentation/ technical writing Expert in Ophthalmic Domain An engineering technical writing resource to help with documentation of multiple complex integrated systems. The role would be full-time for 12 weeks, and ideal candidates would have a mechanical engineering background with experience reading en
Posted 60+ days ago | Updated 10 hours ago

Research Engineer

University of Pittsburgh

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Pittsburgh, Pennsylvania, USA

Full-time

Job Summary Assists with designing, fabricating, and maintaining research instrumentation. Assists with the development of conceptual project design and instrumentation, software programs, and data collection methods. Assists with conducting research. Conducts laboratory procedures, develops software for analysis, and implements robotic equipment protocols. Coordinates work of students and interns. Essential Functions The University of Pittsburgh Department of Neurological Surgery is in searc
Posted 13 days ago | Updated 10 hours ago

Associate Manager, Data Validation Engineer

Takeda pharmaceutical

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Boston, Massachusetts, USA

Full-time

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 Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by
Posted 14 days ago | Updated 10 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Cambridge, Massachusetts, USA

Full-time

Responsibilities: Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal al study data as tables, listings, and graphs for electronic submission to regulatory agencies. Attending multi-disciplinary team meetings, representing the programmi
Posted 4 days ago | Updated 10 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Newark, New Jersey, USA

Full-time

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.
Posted 2 days ago | Updated 10 hours ago

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

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Durham, North Carolina, USA

Full-time

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming support i
Posted 8 days ago | Updated 10 hours ago

Sr. Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Newark, New Jersey, USA

Full-time

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and ADaM specifications. Create and validate SDTM data sets. Create and validate analysis data sets. Create and validate patient profiles. Program and generate tables, figures, and listings (TFLs). Validate and document SAS programs and outputs. Fulfill ad-hoc analysis requests. Provide other services. Requirements: Ba
Posted 12 days ago | Updated 10 hours ago