- LabCorp (Indianapolis, IN)
- …The Histotechnologist I is accountable for the histology handling/storing of precious clinical trial specimens. The Histotechnologist supports the various teams ... and re-embedding of human tissue specimens from patients enrolled in clinical trials. Perform routine, special stains, and advanced staining assays according… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** Reporting to the Head/Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial ... corporate functions to embed diversity into study design and site selection. The Associate Director will build...internal operations under the leadership of the Head of Clinical Trial Diversity + Primary focus is… more
- Abbott (Austin, TX)
- …and liberate more than 500,000 people with diabetes from routine fingersticks. The ** Associate Manager of Clinical Trial Reimbursement** is responsible for ... implementing and managing clinical trial reimbursement processes to secure Medicare and private payer...Informed Consent Forms (ICF) that support IDE, PAS/PMS and single- site clinical trials. + Create study-level Medicare… more
- Actalent (Lexington, MA)
- Job Title: Clinical Trial Associate As a Clinical Trial Associate , you will support clinical operations and contribute to groundbreaking ... clinical research operations and ensure compliance with clinical trial protocols. + Maintain and organize...meetings and lunch. Candidates must be local for occasional on- site meetings. The role requires flexibility for some international… more
- Bristol Myers Squibb (Princeton, NJ)
- …decision-making throughout execution. You will apply a strong foundation in both clinical trial science and applied analytics - from understanding protocol ... Lead study optimization analytics, including assessment of patient and site burden, competitive trial landscape, and other...trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision… more
- J&J Family of Companies (Jacksonville, FL)
- …are searching for the best talent to join our Vision team as a **Staff Clinical Trial Specialist** located in **Jacksonville, FL** Fueled by innovation at the ... ensuring that operating procedures and company policies are followed. The Staff Clinical Trial Specialist develops and manages timelines, resourcing, and budget… more
- Sumitomo Pharma (St. Paul, MN)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- ICON Clinical Research (NC)
- Clinical Site Associate : Looking for candidates...at ICON, you will play a pivotal role in supporting clinical trial operations by ensuring site ... to shape the future of clinical development. ** Clinical Site Associate (CSA)** **Open...+ Follow-up on action items Document Management: + Maintain Trial Master File (TMF) **Your profile** + Bachelor's degree… more
- Kelly Services (Irvine, CA)
- …analyses and publications + If applicable, as part of a clinical trial , may assist in providing on- site procedural protocol compliance and data collection ... and Clinical FSP is currently seeking a Associate Clinical Research Specialist for a long-term...trial materials + May interface and collaborate with site personnel, IRBs/ECs, contractors/vendors, and company personnel + Assists… more
- Cedars-Sinai (Los Angeles, CA)
- …Letters, etc in accordance with local and federal guidelines. + Assists with clinical trial budgets and patient billing. + Responsible for sample preparation ... **Job Description** **Come join our team!** The Clinical Research Associate II works independently...Associate II - Women's Research Program - Full-Time, On- Site **Department** : Womens Cancer Program - WCP **Business… more
- Parexel (Austin, TX)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- … Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ... IVRS set-up, central lab set-up, and other vendor selection processes. + Maintaining clinical trial management system (CTMS) information pertaining to the study… more
- ICON Clinical Research (PA)
- …a Clinical Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + Proven ability to manage multiple ... Senior Clinical Research Associate ICON plc is...and site management, with proficiency in relevant clinical trial software and tools. + Excellent… more
- IQVIA (Philadelphia, PA)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is… more
- ThermoFisher Scientific (Carlsbad, CA)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant...(comparable to **10 Months - 2 years as traveling clinical research associate ** ). Valid driver's license… more
- ThermoFisher Scientific (West Hills, CA)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC...(comparable to 10 Months - 2 years as traveling clinical research associate ). Valid driver's license where… more
- Parexel (Boston, MA)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Astellas Pharma (Northbrook, IL)
- …**Purpose and Scope:** This position is accountable for the direct management of assigned monitoring/ site management related clinical trial staff across all ... clinical monitoring staff + May lead process improvements relevant to clinical trial monitoring and site management + Contribute to development and… more
- Taiho Oncology (Princeton, NJ)
- …biological sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- AbbVie (Nashville, TN)
- …of choice in clinical trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working to improve data ... staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment...+ Ensures audit and regulatory inspection readiness at assigned clinical site at all times. + Manages… more
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