PPD is seeking an experienced Clinical Research Associate to support an Alzheimer’s clinical research program. The role involves clinical monitoring and site management, ensuring protocol and regulatory compliance, data quality, audit readiness, and effective collaboration with investigational sites and project teams. Tags Health Care Life Science Pharmaceutical Artificial Intelligence (AI) Accounting Human Resources
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26 roles found
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Clinical Research Coordinator B/C
$53K/yr – $63K/yr
The University of Pennsylvania, a prestigious Ivy League institution, is seeking a Clinical Research Coordinator B/C to manage clinical trials in the department of Radiation Oncology. This role involves coordinating trial activities, ensuring regulatory compliance, and supporting patient enrollment and data collection. Responsibilities Coordinate trial related activities to ensure the execution of the trials adheres
Clinical Research Coordinator B/C (Abramson Cancer Center)
$53K/yr – $61K/yr
The University of Pennsylvania is a prestigious institution known for its leadership in education and research. The Clinical Research Coordinator B/C will play a vital role in executing clinical trials at the Abramson Cancer Center, ensuring compliance with protocols and federal regulations while supporting the research team in various capacities. Responsibilities Plan, organize, and contribute to study-related meeti
FSP Clinical Research Associate
Competitive
ClinLab Solutions Group is hiring a field-based FSP Clinical Research Associate to monitor clinical trial sites from qualification through close-out. The role ensures protocol compliance, data quality, subject safety, site performance, and audit-ready documentation, with heightened vigilance for CNS and psychiatry trials. Responsibilities Conduct site qualification, initiation, interim monitoring, and close-out visit
Product Owner with Clinical Trial domain
Competitive
Iris Software is recruiting for an unnamed client seeking a Product Owner for a clinical trial platform. The role defines product vision and roadmaps, leads feature development, and supports end-to-end clinical trial workflows while ensuring compliance and measurable product value. Tags Analytics Big Data Information Technology Software Hiring Manager Ankit Grover Insider Connection @Iris Software Inc. 2 email credit
Senior Clinical Research Associate
Competitive
ICON plc is hiring a Senior Clinical Research Associate or Clinical Research Associate II to support clinical trials. The role conducts site visits, ensures protocol compliance, data integrity, and patient safety, collaborates with study sites, reviews clinical data, and contributes to study documentation. Responsibilities Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
CMC Regulatory Affairs Associate (M3 Authoring experience for Biological products ) Tags 63 FAIR MATCH Experience Level 100 Skill 49 Industry Exp. 68 Clinical Trials Pharmaceutical Biotechnology Consulting Responsibilities The Senior Regulatory Associate will author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs, including responses to Health Authority requests Responsibil
Senior Clinical Research Associate (level dependent on experience) jobs in United States Tags 25+ applicants Original Job Post CTI Clinical Trial and Consulting Services 65 FAIR MATCH Experience Level 100 Skill 27 Industry Exp. 76 Pharmaceutical Responsibilities Manages investigative site activity for multiple protocols / indications and provides ongoing updates of site status to Project Manager / sponsor Creates and
Parexel is a clinical research organization supporting clients and advancing clinical research projects. The Project Leader or Senior Project Leader will lead global clinical trial project teams, manage day-to-day operations, and deliver studies on time, within budget, and to high-quality standards while exceeding client expectations. Responsibilities Individuals selected for these roles will provide leadership to pr
(Senior) Program Manager - Toxicology
$110K/yr – $130K/yr
WuXi AppTec is a leading global pharmaceutical and medical device technology platform. The Program Manager/Sr. Program Manager will support and manage Toxicology BU clients’ IND programs, overseeing drug development progress while collaborating with various teams across the U.S. and Europe. Responsibilities Work independently or under supervision in a highly motivated program management team and dynamic environment P
Project Leadership – Biotech (clinical trials) – Immunology / Infectious Disease - Home Based
Competitive
Project Leadership – Biotech (clinical trials) – Immunology / Infectious Disease - Home Based Tags 62 FAIR MATCH Experience Level 72 Skill 46 Industry Exp. 68 Clinical Trials Pharmaceutical Biotechnology Consulting Responsibilities Provide leadership to project teams and manage the day-to-day operations Strive to achieve operational excellence through on time delivery within budget and to the highest quality Exceed c
Project Leadership – Biotech (clinical trials) –Respiratory - Home Based jobs in United States Tags < 25 applicants Original Job Post Parexel 65 FAIR MATCH Experience Level 72 Skill 52 Industry Exp. 68 Clinical Trials Responsibilities Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time deliv
Clinical Research Associate II or Senior
Competitive
Parexel is a clinical research organization specializing in delivering life-changing medicines through clinical research. The Clinical Research Associate II or Senior will monitor clinical trial sites, build investigator and site relationships, manage study documentation, collaborate with cross-functional teams, and maintain compliance and study integrity. Responsibilities Monitor clinical trial sites through on-site
Clinical Trial Manager - USA
$100K/yr – $135K/yr
Linical is seeking a Clinical Trial Manager to oversee clinical study activities and deliverables. The role manages study start-up, clinical monitoring, regulatory compliance, CRA performance, vendors, budgets, milestones, and communications while ensuring adherence to protocols, ICH GCP, SOPs, and applicable regulations. Responsibilities Develops the Site Activation Plan and customizes study start-up documents as ne
Project Leadership – Biotech (clinical trials) –Dermatology - Home Based jobs in United States Tags 75+ applicants Original Job Post Parexel 77 GOOD MATCH Experience Level 72 Skill 84 Industry Exp. 68 Clinical Trials Responsibilities Provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest qualit
Clinical Research Associate II/Sr. Clinical Research Associate - West Coast - FSP Tags 83 GOOD MATCH Experience Level 100 Skill 81 Industry Exp. 68 Clinical Trials Pharmaceutical Biotechnology Consulting Responsibilities Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and qu
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available
$67K/yr – $125K/yr
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available Tags $67K/yr - $125K/yr 78 GOOD MATCH Experience Level 100 Skill 64 Industry Exp. 70 Health Care Life Science Biotechnology Responsibilities Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site process
Clinical Research Associate
Competitive
Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies to improve outcomes for patients with blood cancer. The Clinical Research Associate will monitor clinical studies at investigative sites or remotely, ensuring trials are conducted, documented, and reported according to protocols, SOPs, ICH-GCP, and applicable regulations. Responsibilities May serve as the primary monitor an
Sr./Clinical Trial Manager
$180K/yr – $195K/yr
Responsibilities Support the development, maintenance, and execution on detailed study operational plans, timelines, enrollment projections, and tracking tools in alignment with program strategy and Director guidance Responsible for vendor oversight activities, for assigned vendors, including deliverables, performance metrics, issue resolution, meeting governance, invoices, and scope tracking; supports vendor selecti
Project Leadership – Biotech (clinical trials) – Oncology - Home Based jobs in United States Tags 50+ applicants Original Job Post Parexel 74 GOOD MATCH Experience Level 72 Skill 76 Industry Exp. 68 Clinical Trials Responsibilities Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery
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