- UPMC (Cumberland, MD)
- …with Radiologists regarding protocol development . + Performs or assists Clinical Specialist in performing QA, regulatory testing, and other technical and ... based on their individual experience and education. **Responsibilities:** + Maintains clinical competency for all exams and equipment. + Identifies all patients… 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 ).* Following...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 ... Center (UMGCCC) has an exciting opportunity for a full-time Clinical Research Specialist for the Solid Tumor...them through procedures and visits required by the research protocol . The Research Specialist is also responsible… 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
- 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
- Edwards Lifesciences (Irvine, CA)
- …conduct literature searches and complete literature reviews for design concept, product development , protocol preparation, clinical risk assessments and/or ... journey. **How you'll make an impact:** + Ensures product development includes all necessary clinical input and aspects for the best interest of patients… 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
- 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
- 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
- Medtronic (Mounds View, MN)
- … clinical trial budgets. + Participates in overall clinical management plan, protocol and case report form development . + May be responsible for ... Change Lives** In this exciting role as an Associate Clinical Research Specialist within the Cardiac Rhythm... clinical study site management on a key clinical program to support the development and… more
- Cedars-Sinai (Beverly Hills, 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
- Cleveland Clinic (Cleveland, OH)
- The Clinical Specialist will be responsible for rounding with the inpatient Lymphoma/Myeloma services and for rotation into the outpatient Lymphoma and Multiple ... a post-graduate year 1 residency (PGY-1) plus 3 years of experience as a clinical specialist or equivalent role which includes providing pharmaceutical care and… 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
- Community Health Network (Indianapolis, IN)
- …a career with Community. **Make a Difference** The Clinical Research Specialist will be responsible for the development and implementation of recruitment ... Clinical Research Specialist Job Ref 2402890...associated data entry and source documentation in accordance with protocol guidelines, GCP, ICH, local, state and federal standards… more
- Cedars-Sinai (Los Angeles, CA)
- …a timely manner. + Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form ... use your skill with an organization known nationally for excellence in research!** The Clinical Research Specialist I provides clinical research expertise by… more