- ThermoFisher Scientific (Boston, MA)
- …maintenance, close out, and database lock, depending on the client's needs. Client-dedicated Clinical Trial Associate (FSP CTAs) work directly with clients ... clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy… more
- US Tech Solutions (Cambridge, MA)
- …on TMFs to ensure completeness and readiness for audit/inspection + Contributes to clinical trial excellence initiatives **Main responsibilities and tasks** + Be ... responsible for **setting-up, monitoring verifying and archiving** the ** clinical Trial Master File (TMF)** + In... study creation and set-up for the country and site binders and the trial milestones. +… more
- Lilly (Indianapolis, IN)
- …proofs. + Review/approve allowable dating, stability justifications and retest dating for clinical trial (CT) Materials. + Provide Quality oversight for ... for providing quality oversight of all materials used in clinical trials. PRD QA CT Packaging is responsible for...as needed. + Assist with regulatory body audits and site self-inspections to ensure cGMP compliance. + Provide guidance… more
- Eurofins (West Point, PA)
- …with us today! POSITION SUMMARY: We have an exciting opportunity for a leader with a clinical trial background to help stand up a lab in collaboration with our ... team of ~60 PSS employees for a PSS client site . POSITION RESPONSIBILITIES: + Support Associate Technical...years of experience + Management and training experience + Clinical trial experience + Experience working with… more
- Actalent (New York, NY)
- …creation, and ensure compliance with quality measures and timelines. + Monitor clinical trial performance and quality metrics, escalating issues and proposing ... and provide expert-level guidance. The position reports to an Associate Director and involves both strategic planning and operational...Qualifications + 7+ years of experience as a GLOBAL Clinical Trial Manager with a pharmaceutical or… more
- Cedars-Sinai (Los Angeles, CA)
- …patients with cancer! **Join our team and contribute to groundbreaking research!** The Clinical Research Data Associate II manages the data for assigned research ... analysis, and work with bioinformatics to develop and maintain trial management systems. Ensures compliance with all federal and...and beyond. **Req ID** : 8440 **Working Title** : Clinical Research Data Associate II - The… more
- J&J Family of Companies (Santa Clara, CA)
- …more at https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical Trial Project Management **Job Category:** Professional **All Job ... Description:** Johnson & Johnson is hiring for a **Principal Clinical Research Associate - Shockwave Medica** l...study preparation activities, as applicable. + Develops and revises clinical trial documentation including clinical … more
- AbbVie (Chicago, IL)
- …This role will be assigned investigative sites in the Chicago, IL area. Focus on site clinical research that ensures appropriate conduct of the trial while ... 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 investigator… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …& Logistics (SP&L) function with assigned tasks related to steady supply of Clinical Trial Materials (CTM). **Responsibilities** + Lead the authoring, revising, ... authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will… more
- Taiho Oncology (Princeton, NJ)
- Study Associate I, Clinical Operations Princeton, NJ,...Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site ... 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
- Takeda Pharmaceuticals (Boston, MA)
- …(CRO) (ie, the Clinical Research Associate (CRA)). The Associate Director, Study Site Engagement establishes communication with regional/country Medical ... specific strategies. + The Associate Director, Study Site Engagement supports study teams with trial ...the direction of Clinical Programs. + The Associate Director, Study Site Engagement supports Takeda… more
- Mount Sinai Health System (New York, NY)
- …Experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is highly desirable. **Responsibilities** ... Research Associate I monitors all aspects of clinical research trial (s) Clinical study life-cycle responsibilities including site management, ongoing… more
- Abbott (Alameda, CA)
- …members, peers, and management. + Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical ... business needs. + Conduct single or multi-center medical device clinical studies. + Perform study site visits...required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and… more
- Danaher Corporation (Chaska, MN)
- …degree in the life sciences or related field required with 5+ years of clinical trial experience in vitro diagnostics (IVD), medical device, or healthcare ... diagnostic tools that address the world's biggest health challenges. The Senior Clinical Research Associate for Beckman Coulter Diagnostics is responsible for… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- **Job Description Summary** Associate Clinical Project Manager / Senior CRA collaborates with the core tea, clinical and medical affairs associates ... candidate to join our team! The role of the Associate Clinical Project Manager/Senior Research Associate...for the coordination and management of all aspects of clinical trial conduct including (but not limited… more
- Avania (OR)
- …you will be the lead for several studies running in parallel, in all associated clinical trial phases, from regulatory submissions to close out visits, from ... Avania are hiring for the key role of experienced Clinical Research Associate (CRA) or Senior ...communication and comradery. We offer a full range of clinical trial services in the Asia Pacific… more
- Allogene (South San Francisco, CA)
- … Clinical Operations, to oversee the successful completion management of all clinical trials and related clinical trial milestones within established ... development of study protocols, oversee and manage CROs, manage clinical study start-up and execution including site ...Operations experience, with a minimum of 5 years leadership clinical trial management experience * Cell therapy… more
- WuXi AppTec (Austin, TX)
- …position within the Operations team and is assigned as a study lead to manage clinical trial studies. The Senior CRA will partner with a Project Manager to ... CRA will work to manage, oversee and may monitor/co-monitor clinical trial sites. **Essential Job Functions:** +...Education:** + Minimum of 4 years experience as a Clinical Research Associate in the pharmaceutical/biotech or… more
- Lilly (Indianapolis, IN)
- …compliance oversight and batch release for Product Research and Development (PR&D) Clinical Trial activities manufactured at Collaboration Partners (CPs). The ... other quality related activities. **Scope:** Large and Small Molecule products, clinical trial manufacturing and associated collaboration partners, Product… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Position is Project Manager for a large multi- site clinical trial . Train and oversee CRA's on the project. Clinical Site is also ... Coordination Center for the clinical trial . Manage all aspects of the clinical...Level including but not limited to: Procuring study drug, site selection and management, vendor selection, consent form development,… more