Clinical trials jobs in philadelphia, pa

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

Associate Director, Biostatistics

King of Prussia, Pennsylvania

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Today

Position Purpose: 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. (There are 2 positions available supporting multiple Therapeutic Areas) Work Environment: This is a hybrid position with a minimum of 3 days onsite in the designated work location weekly.

Full-time

Clinical SAS Programmer

King of Prussia, Pennsylvania

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10d ago

Design, develop, and validate statistical programs, datasets, and reporting outputs (tables, listings, and figures) for clinical trials in alignment with project requirements and regulatory standards. Build and maintain analysis datasets (ADaM) and study data tabulation models (SDTM) in compliance with CDISC standards, ensuring traceability and submission readiness. Develop, maintain, and optimize SAS programs, macros, and templates for clinical data review, reconciliation, and reporting to supp

Full-time

Director, Portfolio Development Process & Standards Lead

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 Director, Portfolio Development Process & Standards Lead? This position is located in our King of Prussia, PA Waltham M

Full-time

Compensation information provided in the description

Senior Principal EA Research Technology

Philadelphia, Pennsylvania

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Today

Description Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across all disciplines. Today at Penn Medicine, someone will make a breakthrough. Someone will heal a heart, deliver hopeful news, and give comfort and reassurance. Our e

Full-time

Depends on Experience

Director, Portfolio Development Process & Standards Lead

King of Prussia, Pennsylvania

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Today

Full-time

Compensation information provided in the description

Senior Engineer, Human Factors

Malvern, Pennsylvania

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Today

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

Full-time

Principal Engineer, Human Factors

Malvern, Pennsylvania

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Today

Full-time

USD 117,000.00 - 201,250.00 per year

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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6d ago

Director/Senior Director - CRO Solutions & Product Strategy Company: Saama Function: Product / Solutions Level: Director or Senior Director Location: Europe remoteRole Overview Saama is seeking an experienced clinical research and CRO leader to help shape the next generation of AI-powered solutions for Contract Research Organizations (CROs). This individual will serve as the vital bridge between Saama''s Product organization and our CRO customers and prospects. The ideal candidate has spent sig

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Full-time, Third Party

Depends on Experience

Product Manager - Veeva Vault

Remote

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9d 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

Contract role: Senior Clinical SAS Developer at North Wales, PA (Onsite) - C2C

Hybrid in North Wales, Pennsylvania

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Today

Senior Clinical SAS Developer Upper Gwynedd, PA (Onsite) C2C is fine Looking for SDTM experts having in-depth knowledge of SAS programming(macro's) Must have 10+ yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point of contact for biostatisticians and study teams Perform peer review of code and documentation for accuracy and traceability Review CRF (Case Report Form) annotatio

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Contract, Third Party

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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5d 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

Clinical trials jobs in Philadelphia, PA, USA