- George Washington University (Washington, DC)
- …the medical record, computer-coded or on-line data form, and appropriate research protocol forms. Pursues a program of professional development ; participates in ... cases.The National Capital Poison Center is seeking a Poison Information Specialist to provide telephone toxicologic consultations to public and health professional… more
- FUJIFILM Holdings America Corporation (Atlanta, GA)
- …observations/trouble shooting, product retirement.Work with sales/sales leadership, national business development managers, clinical specialist team, and ... heritage with cutting-edge AI innovations to inspire a new tier of clinical confidence. The In-Vitro Diagnostic portfolio provides the golden standard of molecular… more
- George Washington University (Washington, DC)
- …with Office of Research Integrity and Compliance leadership, the Office of Clinical Research (OCR) staff, Environmental Health and Safety, Office of General Counsel, ... position is accountable for employee engagement, adequate staffing levels, budget development and compliance, staffing decisions such as hiring and terminating… more
- Mayo Clinic (Rochester, MN)
- …of pre-written protocol / clinical research documents through the clinical trial development /implementation process; writing of the informed consent ... to succeed. **Responsibilities** Independently executes the overall management of the clinical trial development , maintenance, and completion process. Directs… more
- University of Maryland, Baltimore (Baltimore, MD)
- …Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPPA) protocol development and ensure compliance of research operations with ... is currently recruiting for a full-time Bone Marrow Research Specialist ( Clinical Research Specialist ).* **...them through procedures and visits required by the research protocol . The Bone Marrow Research Specialist is… more
- University of Maryland, Baltimore (Baltimore, MD)
- …Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPPA) protocol development and ensure compliance of research operations with ... Cancer Center (UMGCCC) has an exciting opportunity for a full-time Clinical Research Specialist for the Hematologic Malignancies research program.*This… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Research Specialist A/B (Infectious Disease Clinical Trials Group) Job Profile Title ... Research Specialist A: Learning and abiding by laboratory SOPs, protocol specific lab manuals, and reviewing changes as they occur. Working closely… more
- University of Maryland, Baltimore (Baltimore, MD)
- …Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPPA) protocol development and ensure compliance of research operations with ... them through procedures and visits required by the research protocol . The Research Specialist is also responsible...theCOVID-19 website. *Essential Functions* * Performs as a single Specialist in a clinical setting who is… more
- Johns Hopkins University (Baltimore, MD)
- …Experience in clinical research and regulatory affairs. + Experience in protocol and informed consent writing, data analysis, grant writing, and /or manuscript ... for other projects within our program. This includes the development of laboratory manuals and the design of biospecimen...financial management of clinical trials. Classified Title: Clinical Research Program Specialist Job Posting Title… more
- Cedars-Sinai (Beverly Hills, CA)
- …in a timely manner. Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form ... to having you join our team to collaborate on groundbreaking research!** The Clinical Research Specialist provides clinical research expertise by… more
- Edwards Lifesciences (Irvine, CA)
- …conduct literature searches and complete literature reviews for design concept, product development , protocol preparation, clinical risk assessments and/or ... in Irvine, Ca with travel up to 25% nationwide.Ensures product development includes all necessary clinical input and aspects for the best interest of patients… more
- Kelly Services (Irvine, CA)
- …+ Supports the clinical study team in the development of clinical trial documents (eg study protocol , informed consents, CRF, monitoring plan, study ... Clinical FSP is currently seeking an Associate Clinical Research Specialist for a long-term engagement...personnel, IRBs/ECs, contractors/vendors, and company personnel; + Assists the clinical study team in overseeing the development … more
- Corewell Health (Grand Rapids, MI)
- Clinical Research Specialist - All of Us Research Program. With principal investigator oversight, prepares, evaluates and implements research studies to enhance ... studies for implementation including: assessment of operational feasibility; budget development ; preparation of IRB documents; institutes protocol operations… more
- Dignity Health (Phoenix, AZ)
- …community we are proud_ _to be_ _a tobacco-free campus._ **Responsibilities** This Clinical Research Specialist (Coordinator) position is specific to the ... and additionally is a national leader in managing national and international ALS clinical trials. The ALL ALS consortium will collect clinical and biomarker… more
- Abbott (New York, NY)
- …that advance the standard of care. The job purpose and scope of the Structural Heart Clinical Lead Specialist (CLS) is an integrated part of clinical trials ... to be an extension for field preceptorship initiatives. The Clinical Lead Specialist is to support Abbott...and patient outcomes. + Providing trial site education of clinical trial protocol , inclusion, and exclusion criteria.… more
- University of Rochester (Rochester, NY)
- …equivalent clinical experience. This may be a new resident graduate or a clinical specialist in the first 3-5 years of practice. Doctor of Pharmacy degree, ... GENERAL PURPOSE: The toxicology clinical pharmacy specialist is responsible for...and maintain innovative disease or medication management programs and clinical pharmacy services. + Participates in the development… more
- Kelly Services (Irvine, CA)
- …trial sites (eg site management)** + **Contribute towards development of clinical trial documents (eg study protocol , informed consents, CRF, monitoring ... ** Clinical Research Specialist (Hybrid)** **SUMMARY:** **This...assigned projects.** + **If applicable, as part of a clinical trial, may provide on-site procedural protocol … more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trials Manager ... protocol and/or informed consent form modifications, and assisting Clinical Trials Manager and coordination team with startups and...a cure from conceptual bench research, to prototyping and development , to clinical trials and FDA approval.… more
- Cedars-Sinai (CA)
- …a timely manner. + Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form ... **Job Description** The Clinical Research Specialist I provides ...Responsible for specific and assigned aspects of research infrastructure development , coordinates projects, and communicates status and improvement areas… more
- Abbott (Chicago, IL)
- …working mothers, female executives, and scientists. **WHAT YOU'LL DO** The Leadless Clinical Specialist provides technical, clinical , educational and sales ... full life. You'll also have access to: + Career development with an international company where you can grow...adoption and growth of Abbott leadless technology. The Leadless Clinical Specialist works closely with internal and… more
