- IQVIA (Parsippany-Troy Hills, NJ)
- …inspection readiness, and uphold GCP, SOP, and local regulatory standards.Two years of clinical trial management experience is required within a role that is ... Trial Managers are an integral part of clinical trial delivery, liaising with clinical...activities to bring revenue forward in partnership with the senior project leader.Identify changes in scope and partner with… more
- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …4 Year Degree Salary Range $85000.00 - $110000.00 Salary Description Job Title: Senior Associate , Clinical Research Supervisor/Manager Title: Senior ... Manager, Clinical Affairs Job Description Summary: The Senior Clinical Research Associate will...Required Education and Experience: 2+ year of experience in clinical trial research is required (preferred in… more
- Amgen (Washington, DC)
- …clinical trial experience OR + Bachelor's degree and 6 years of statistical clinical trial experience OR + Associate 's degree and 10 years of ... clinical trials safety assessment. As a Safety Statistician, Senior Manager, your key activities will include: + Represents...Qualifications:** + Doctorate degree and 2 years of statistical clinical trial experience + Master's degree and… more
- ICON Clinical Research (New York, NY)
- Senior Clinical Research Associate ...Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + ... clinical development. We are currently seeking a Senior Clinical Research Associate (CRA)...will play a critical role in overseeing and managing clinical trial activities to ensure they are… 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 ... . **Position Summary** The TAIP Principal Analyst is a mid- senior level role within Bristol Myers Squibb's Trial...trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Sr . Principal Associate Quality Excellence and Inspection Readiness is responsible for partnering with the Compliance Leader to provide technical… more
- University of Miami (Miami, FL)
- …institutional guidelines, tissue dissection, primary tissue culture. Assists in Phase I clinical trial related sample receipt, handling and documentation with ... SCCC has an exciting opportunity for a Full Time Sr . Research Associate 3 to work at...of our lab is to generate preclinical data for clinical translation. Relevant experience in immunology, cell biology, molecular… more
- Penn Medicine (Philadelphia, PA)
- …our future each day. Are you living your life's work? Job Title: Sr Administrative Services Associate Department: Otorhinolaryngology Location: Hospital of the ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
- Penn Medicine (Philadelphia, PA)
- …shape our future each day. Are you living your life's work? Job Title: Sr Administrative Services Associate Department: EPS Lab Location: Hospital of the ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
- Amgen (Washington, DC)
- …development and execution of the patient recruitment & retention (PRR) and decentralized clinical trial (DCT) strategies in partnership with clinical program ... the lives of patients while transforming your career. **Patient Recruitment & Retention Senior Manager** **What you will do** Let's do this. Let's change the world.… more
- IQVIA (Overland Park, KS)
- …Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and ... phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local… more
- ThermoFisher Scientific (Indianapolis, IN)
- …team, you will timely and accurately assemble and/or label pharmaceutical clinical trial treatments and supplies following all associated manufacturing ... Information:** Indianapolis, Indiana Thermo Fisher Scientific run's the World's largest clinical packaging operation. Our Clinical Trials facilities are… more
- BeOne Medicines (Emeryville, CA)
- …with CRAs to ensure data collection is met per contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to ... Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes with a thorough knowledge of ICH and… more
- IQVIA (Carlsbad, CA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- AbbVie (Montgomery, AL)
- …issues that could affect timelines and develop alternative solutions. + Ensure clinical trial management systems containing all site-specific information are ... Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Senior CRA will enable AbbVie' s emergence as a world class R&D… more
- IQVIA (Philadelphia, PA)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within...activities to bring revenue forward in partnership with the senior project leader. + Identify changes in scope and… more
- Hartford HealthCare (Hartford, CT)
- …they turn to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal ... for the overall design, conduct, and management of the clinical trial , the SrCRA leads, facilitates and...all aspects of study activity as required of a Clinical Research Associate This is a grant… more
- Abbott (Minneapolis, MN)
- …Summary Under the supervision of senior colleague/manager (or delegate), the Associate Clinical Site Lead drives study execution and operational excellence ... (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and ...a level that allows for appropriate collaboration with Abbott clinical staff, eg Site CRA, Site Contract Associate… more
- Merck (Upper Gwynedd, PA)
- …way we approach serious diseases. The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial … more
- Abbott (Alameda, CA)
- …members, peers, and management. + Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical ... procedures and applicable regulatory requirements. + Responsible for assisting senior staff in planning study conduct, designing case report...required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and… more
