Clinical trials jobs in madison, wi

Consultant, Clinical Supplies Management, Biopharma, Global Trials

Remote or Almont, Colorado

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Today

Description: CONTEXT & INITIATIVE DESCRIPTION Our BioPharma Client is seeking a Consultant, Clinical Supplies Management to support the planning and execution of global Phase I- clinical trials. This critical Consultant will play a key role in ensuring the timely availability, packaging, distribution, and ongoing management of clinical trial supplies across sites and depots. The ideal candidate will have strong clinical supply and trial operations experience, excellent cross-functional communi

Contract

Senior Engineer - Engineering, Equipment

Madison, Wisconsin

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Today

Senior Engineer - Engineering, Equipment Position Summary Shift: Monday - Friday 8:00am - 5:00pm100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With tim

Full-time

Engineer - Engineering

Madison, Wisconsin

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Today

Engineer (Facilities) Position Summary: Work Schedule: M-F 8am-5pm100% on-site Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex developm

Full-time

Manager - Engineering

Madison, Wisconsin

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Today

Manager - Engineering Position Summary: Work Schedule: M-F 8am-5pm100% on-site Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI,and our market leading biologics analytical services in Kansas City, MO and Res

Full-time

Associate Engineer - Engineering

Madison, Wisconsin

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Today

Associate Engineer - Engineering About Site Catalent's Madison, Wisconsin site is a state-of-the-art biologics development and manufacturing facility supporting customers from research through early- and mid-stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single-use systems to enable rapid

Full-time

Principal Process Engineer - Manufacturing Sciences & Technology, Upstream

Madison, Wisconsin

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Today

About Site Catalent's Madison, Wisconsin site is a state-of-the-art biologics development and manufacturing facility supporting customers from research through early- and mid-stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single-use systems to enable rapid scale-up and customization. The s

Full-time

Process Engineer - Engineering

Madison, Wisconsin

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Today

Process Engineer - Engineering About Site Catalent's Madison, Wisconsin site is a state-of-the-art biologics development and manufacturing facility supporting customers from research through early- and mid-stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single-use systems to enable rapid s

Full-time

Process Engineer - Manufacturing Sciences & Technology

Madison, Wisconsin

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Today

Process Engineer - Manufacturing Sciences & Technology (MS&T), Downstream Technology Transfer Position Summary: Work Schedule: Monday - Friday, core hours 8am-5pm100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufactur

Full-time

Clinical Research Scientist III - (Director/Assoc. Director level)

Remote or Hybrid in Parsippany-Troy Hills, New Jersey

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10d ago

Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. Participates in protocol review discussions concerning scientific and procedural aspects of study design. Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision. With supervision, contributes to the design and development of CRFs, Data Management Manuals and Da

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Third Party, Contract

$100 - $110

Director/Senior Director - CRO Solutions & Product Strategy

Remote

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Today

Director/Senior Director - CRO Solutions & Product Strategy Company: Saama Function: Product / Solutions Level: Director or Senior Director Location: Europe remoteSaama is an AI and advanced analytics company built for life sciences. Best known for the AI-powered clinical platform that supported the trial behind the world''s first COVID-19 vaccine, Saama works with many of the top 20 pharmaceutical companies and a large base of emerging biotechs. Alongside our clinical development portfolio, we

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Full-time, Third Party

Depends on Experience

Product Manager - Veeva Vault

Remote

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10d ago

Role: Veeva Vault Product Manager Location: Remote Job Type: FTE/ Full- Time Experience Range: 10- max 22 years Primary Skills: 1. Experience with system integrations (e.g., CTMS eTMF/EDC/Data Lakes & repositories) 2. Experience working with Siebel (CTMS) 3. Experience working with Veeva Managed Services or vendor escalations 4. Familiarity with Agile or DevOps methodologies 5. Knowledge of clinical metrics and reporting tools Required Bachelors degree in Life Sciences, Information Systems, o

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Full-time

Depends on Experience

Business Analyst – Clinical/Life Sciences

Remote

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5d ago

Business Analyst Clinical/Life SciencesIntroduction: This Business Analyst position in the Clinical/Life Sciences industry requires a professional with strong business analysis and IT delivery experience. The ideal candidate will have expertise in Life Sciences/Clinical Systems such as CRM and CTMS, along with a deep understanding of clinical trial lifecycle and site operations. This role involves translating business requirements into user stories, workflows, specifications, and actionable del

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Third Party, Contract

Depends on Experience

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 with one of our Global MedTech 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. You may also be e

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Contract

Veeva Vault Product Manager

Remote

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6d ago

Veeva Vault Product Manager Clinical SME | Remote | FTE Location: Remote Employment: FTE Experience: 1022 Years We are hiring an experienced Veeva Vault Product Manager / Clinical Systems SME with strong expertise in Veeva Vault Clinical (CTMS & eTMF) and clinical trial operations. Key Requirements: 812+ years of experience delivering/leading regulated enterprise or clinical systems initiatives Deep hands-on experience with Veeva Vault Clinical CTMS & eTMF Strong understanding of clinical tria

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Full-time

Depends on Experience

Implementation Engineer, Digital Diagnostics (DDx)

Remote or Boston, Massachusetts

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8d ago

Who We Are PathAI's mission is to improve patient outcomes with AI-powered pathology. Our platform promises substantial improvements to the accuracy of diagnosis and the efficacy of treatment of diseases like cancer, leveraging modern approaches in machine learning. Our team, comprising diverse employees with a wide range of backgrounds and experiences, is passionate about solving challenging problems and making a huge impact. Where You Fit We're looking for an Implementation Engineer to join

Full-time

USD 48,000.00 - 73,600.00 per year

Veeva Vault Adoption Specialist

Remote

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3d ago

Job Description - Title: Veeva Vault Adoption Specialist Duration: 12+ months Contract Location: Remote MOI: Video Need LinkedIn with profile pic and recent manager references with official email and LinkedIn Must have Veeva, CTMS, ETMF and training experience OBJECTIVES/PURPOSE Work with GDO, R&D and cross-functional stakeholders to collect develop and deploy effective support materials for systems in DSDS ownershipWork with the Business System Owner (BSO) for the system portfolio to identify

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Contract

$40 - $60

Senior Technical Business Analyst

Remote

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5d ago

DescriptionJob Title: Senior Healthcare Business Analyst Type: Part Time Experience Level: Senior Seeking a highly skilled and experienced Senior Business Analyst responsible for bridging the gap between business objectives and technology solutions, ensuring that our projects align with organizational goals and deliver maximum value. You will utilize your expertise in business analysis and data-driven decision-making to identify opportunities for improvement and drive successful project outcomes

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Part-time

Depends on Experience

SME - Reviewer Scientist

Remote

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6d ago

Subject Matter Expert - Reviewer ScientistThe SME - Reviewer Scientist will provide scientific and regulatory expertise in reviewing clinical and nonclinical data submitted in support of drug applications. This position will support projects within the FDA Center for Drug Evaluation and Research (CDER), Office of Computational Science, under the direction of the COR. Responsibilities: Review clinical safety and efficacy studies submitted in support of drug applications. Evaluate clinical and non

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Full-time

Depends on Experience

Clinical Research Specialist

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking a Clinical Research Specialist for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This position is hybrid. 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 ot

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Contract

Senior Director, Light-Track Delivery & AI Automation

Remote

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Today

About Parexel Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, and shared purpose -- moving with urgency to address patient needs and accelerate

Full-time

Clinical trials jobs in Madison, WI, USA