- Daiichi Sankyo, Inc. (Bernards, NJ)
- …outstanding leadership skills based on a sound knowledge of clinical research standards and GCP.Develop operational strategies for ... program. This position will require line management responsibility of Directors, Associate Directors, Clinical Study Managers, who are primarily responsibility… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: This is an ... and approvals and associated interactions with vendors. Supports regular vendor/ sponsor discussions to identify risks and ongoing study support. Identifies… more
- IQVIA (Carlsbad, CA)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Washington, DC)
- …in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- IQVIA (Philadelphia, PA)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws,… more
- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate II **Required Qualifications (as evidenced by an attached resume):** Bachelor's Degree in appropriate field. Three (3) years of ... a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines...of posting.** **Job Number:** 2503665 **Official Job Title:** : Clinical Research Associate II **Job… more
- Rush University Medical Center (Chicago, IL)
- …national origin, disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator (Oak Lawn, IL) ... works under the general direction of the Office of Research Affairs' Clinical Research Administration...and responds to questions from PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Sep 10, 2025 Requisition # 107255 ... The Stanford Stroke Center is seeking a Clinical Research Coordinator Associate to...databases, and regulatory files. + Participate in monitoring visits, sponsor meetings, and regulatory audits, serving as the study… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… more
- Ochsner Health (Covington, LA)
- …bachelor's degree. Preferred - 2 years of experience in area of assigned clinical specialty, managing clinical research and patient databases. ... all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, research ...Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Ability… more
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor /CRO regulatory correspondence. ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… more
- AbbVie (Atlanta, GA)
- …Description The CRA II advances AbbVie's pipeline by striving for excellence in clinical research , turning science into medicine for patients, and leveraging ... build meaningful, effective engagements that position AbbVie as the sponsor of choice in clinical trials. The... clinical trials. The role focuses on site clinical research by ensuring proper trial conduct,… more
- OhioHealth (Columbus, OH)
- … works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice ... regulations. This position performs basic day to day activities related to clinical research studies including: recruit and screen participants, obtains informed… more
- SUNY Upstate Medical University (Syracuse, NY)
- …of education and experience. SoCRA certified or ACRP certified Experience with clinical research protocols, knowledge of medical terminology, computer skills, ... for the clinical trial. Manage all aspects of the clinical trial at the Sponsor Level including but not limited to: Procuring study drug, site selection… more
- Cedars-Sinai (Los Angeles, CA)
- …year of experience as a clinical research coordinator or clinical research associate /assistant preferred. + Demonstrated ability to accurately ... team and contribute to groundbreaking research .** This position functions as a Clinical Research Coordinator providing support for clinical research … more
- Georgetown Univerisity (Washington, DC)
- …(eg, the study monitor appointed by the sponsor for each trial). The Associate Director and the Director of Clinical Trials rely on timely responses from ... to making a difference in the world. Requirements The Clinical Research Coordinator 2 (CRC2) is responsible...a daily basis, the CRC2 will report to the Associate Director of Clinical Trials. The CRC2...to the sponsor contact… more
- Cleveland Clinic (Cleveland, OH)
- …This role manages the full administrative and operational lifecycle of Phase I-IV clinical research trials. Acting as a central coordinator, the position ensures ... clinicians lack in-depth regulatory knowledge. You interact with physicians and investigators, clinical trial sponsors, clinical research team members,… more
- SUNY Upstate Medical University (Syracuse, NY)
- … trial. Duties include but are not limited to: coordinate all aspects of the clinical trial at the Sponsor Level including but not limited to: procuring study ... This role will act as the project manager for a large multi-site clinical trial where the clinical site is also the coordination center for the clinical… more
