clinical trials Jobs

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Python Developer - (clinical data)

Radiant System, Inc

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Remote

Contract

Seeking a Python Developer with strong experience in clinical data standards (SDTM/CDISC) and a background in the pharmaceutical industry. Role involves developing automation pipelines and AI/ML models to transform clinical trial data into SDTM-compliant datasets. Must-Haves: 8+ years in pharma/clinical domain 3+ years Python development SDTM, CDISC, ADaM, raw datasets Experience with AI/ML (NLP, classification) Tools: Pinnacle 21, Define.xml Nice-to-Have: Metadata-driven automation Knowledge of
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Posted 12 hours ago

Sr. Regulatory affairs Consultant-W2 ONLY

VetForce Solutions

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Remote

Contract

Sr. Regulatory affairs Our client is a rapidly expanding biotech company based in China that recently partnered with a major pharmaceutical company for research collaboration efforts, in hopes of discovering and developing novel oral drug candidates across multiple therapeutic indications (oncology, immunology, etc.) Our client is looking to bring on a Senior Regulatory Affairs Consultant (Senior/Director Level), who will provide strategic regulatory guidance as the client navigates the regulato
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Posted 14 hours ago | Updated 14 hours 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 7 days ago | Updated 1 day ago

Clinical Services Project Manager

Software Guidance & Assistance

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Tucson, Arizona, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Services Project Manager for a contract assignment with one of our premier Pharmaceutical clients in Tucson, AZ. Responsibilities : Manages multiple clinical and lab services projects of less complex nature from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interacti
Posted 7 days ago | Updated 4 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 16 days ago

Labware LIMS Specialist

Quantum World Technologies Inc.

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Kent, Connecticut, USA

Full-time, Third Party, Contract

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 11 hours ago

Sr Product Architect - Veeva Vault (ISG)

Cognizant

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Chicago, Illinois, USA

Full-time

Job Title - Sr Product Architect - Veeva Vault Job Summary The Sr Product Architect in ISG will be responsible for designing and implementing robust solutions using Veeva Vault for eTMF and CTMS. With a focus on Cheminformatics and Bioinformatics, the role requires a deep understanding of these domains. The candidate will work in a hybrid model, ensuring seamless integration of systems to enhance business processes and drive innovation. Responsibilities - Design and implement scalable solutions
Posted 18 days ago | Updated 6 hours 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 11 days ago | Updated 6 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 44 days ago | Updated 6 hours ago

RN - HIV Medicine Practice

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 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 medi
Posted 60+ days ago | Updated 6 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 6 days ago | Updated 6 hours ago

Analyst, External Data Acquisition Expert

Johnson & Johnson

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Remote or Pennsylvania, 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 11 days ago | Updated 6 hours ago

Associate Director - Hematology, Oncology Data Sciences & Digital Health

Johnson & Johnson

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Remote or New Brunswick, 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 34 days ago | Updated 6 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 39 days ago | Updated 6 hours ago

Associate Director, Biotherapeutic Engineering & Bioconjugation

Novartis

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San Diego, California, USA

Full-time

Job Description Summary As Associate Director of Biotherapeutic Engineering & Bioconjugation, you will have an opportunity to join the Biologics Research Center (BRC) as a leader at the cutting edge of discovery and development of innovative medicines to address unmet medical needs. BRC builds the biologics pipeline in collaboration with Biomedical Research (NBR) Disease Areas and Platforms via a breadth of technologies for discovery of antibody, protein, gene therapy and RNA-based therapeutics.
Posted 18 days ago | Updated 6 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 6 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 8 days ago | Updated 6 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 9 days ago | Updated 6 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 3 days ago | Updated 6 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Minneapolis, Minnesota, 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 18 hours ago | Updated 6 hours ago