- Dartmouth Health (Lebanon, NH)
- …this position collaborates with research and non-research staff, maintaining involvement throughout the clinical trial process. The role of the Clinical ... Overview The Clinical Research Nurse I performs a variety of...families, they provide care, education and support throughout the trial . Under the supervision of the PI or their… more
- Abbott (Alameda, CA)
- …or Sr. Director, Clinical + Provides input and support for planning post- trial clinical activities and product market launch. + Support all Divisional ... Assessments (NTA). Internally interfaces with data management, biostatistics, regulatory, clinical research associates, trial coordinators, field clinical… more
- BeOne Medicines (San Mateo, 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 ... **General Description:** The SCRA is primarily a site monitor and is responsible for the management and...CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes with a thorough knowledge… more
- University of Colorado (Aurora, CO)
- …protocol Inclusion/Exclusion Criteria, and confirms eligibility of subject to participate in clinical trial . Performs informed consent process or ensures that ... contacts and personal interviews + 5% - Schedules subject participation in research clinical trial , coordinating availability of necessary space, and clinical… more
- Abbott (Alameda, CA)
- …processes. This role is critical to the successful collection, reporting and analysis of clinical trial data as well as the mentorship of junior team members. ... **What You'll Work On** + Assist in translation of clinical study requirements into trial Casebook. +...to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.… more
- University of Colorado (Aurora, CO)
- …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial + Perform informed consent process or ensures that ... phone contacts and personal interviews + Schedule subject participation in research clinical trial , coordinating availability of necessary space, and clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …Job Description Summary This position will assist in the management of a clinical trial and responsibilities in specific research area. Coordinate the ... field with at least 1 year of experience conducting human subjects research, clinical trial / clinical research experience or an equivalent combination of… more
- Bristol Myers Squibb (Princeton, NJ)
- …effective data review, trial status and risk identification. Engagement of clinical trial functions for reporting and analytic needs. Technical SMEs to ... CDR&A is responsible for the ingestion, transformation and delivery of clinical data to internal stakeholders, primarily to Biometrics and Data Sciences.… more
- Cedars-Sinai (CA)
- …Description** **Are you ready to be a part of breakthrough research?** The Clinical Research Coordinator I supports clinical research protocols for the ... Coordinator will assist the Research Department with all aspects of clinical research. This individual will interact with principal investigators, subjects, clinic… more
- Lilly (Indianapolis, IN)
- …world. Purpose: The Associate Director, CTF Clinical Results Systems (as part of Clinical Trial Foundations) is a leader and key partner across the business. ... processes and technology ▪ Knowledge of emerging IT capabilities used for clinical trial data management ▪ Capacity and workload management expertise… more