- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine interaction with key ... and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily a...and delivery of study team plan and milestones (eg protocol , eCRF/EDC, IXRS, Clinical Study Oversight Plan… more
- Eisai, Inc (NJ)
- …is your profile, we want to hear from you. Job Summary The Senior Manager , Medical Writing will be the designated Lead Medical Writer for approximately 3-4 Programs. ... Writer, the incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds' life cycle… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol , Good Clinical Practices (GCPs), ... appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH)… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol , Good Clinical Practices (GCPs), ... appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH)… more
- MD Anderson Cancer Center (Houston, TX)
- …and TMC regulatory area to be aware of upcoming protocols. . Participate in protocol -specific clinical tasks as needed. . Oversee activities of HAL clinical ... professionals, employees and the public. **JOB SPECIFIC COMPETENCIES** **1.** ** Administration and Management** **50%** . Provides administrative management of the… more
- MD Anderson Cancer Center (Houston, TX)
- …meetings. . Responsible for notifying in writing all relevant personnel (ie PIs, Manager , Clinical Protocol Administration , Regulatory Program ... settings for minimal risk studies. . Assesses patients in the inpatient/outpatient clinical setting for follow up appointments per protocol requirements .… more
- University of Southern California (Los Angeles, CA)
- …/Off Study of patients. 9. Assists in training of other Coordinators. B. Protocol Administration 1. Determines patient eligibility a. Schedules necessary tests. ... experienced Registered Nurse and has a strong interest in clinical research. The role of the protocol ...for reporting to the IRB and promptly notifies Data Manager of occurrence of SAE. 5. Interacts with the… more
- University of Colorado (Aurora, CO)
- Clinical Science Program Manager - 33067 University Staff **Description** **University of Colorado Anschutz Medical Campus** **School of Medicine | Department of ... Medicine** **Job Title:** ** Clinical Science Program Manager ** **Position: #00821011 -...coordination and regulatory processes, procedures as defined in study protocol and in compliance with regulating bodies, including but… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (Surgery Research Administration ) Job Profile Title ... Description Summary This position will assist in the management of multiple clinical trials and responsibilities in specific research area. Coordinate the screening… more
- Veterans Affairs, Veterans Health Administration (St. Cloud, MN)
- …professional mental health counselor (LPMHC) assigned to the Mental Health Integrated Clinical Community (MH ICC) spending a portion of time providing various ... i. The incumbent will provide a full range of clinical services which includes case work, individual, family and...assignments, as deemed necessary by the MH Special Programs Manager . n. The incumbent will maintain data and statistical… more
- Albany Medical Center (Albany, NY)
- …DUTIES AND RESPONSIBILITIES - and as supervised under PI / Research Manager /RN oversight where appropriate: Complete and submit protocol specific research ... soundness and logistical capabilities as appropriate Knowledgeable on each protocol 's specific inclusion, exclusion, therapy, clinical monitoring oversight,… more
- University of Rochester (Rochester, NY)
- …of Pulmonary Critical Care, at The University of Rochester is seeking a full-time Clinical Research Manager oversee and manage clinical research. The ... Fibrosis and Lung Scarring, Pulmonary Embolism and Hypoxemic Respiratory Failure. This Clinical Research Manager is responsible for the day-to-day oversight and… more
- University of Colorado (Aurora, CO)
- Clinical Trials Operations Manager - 33671...and Project). + A strong working knowledge of Good Clinical Practices (GCP), US Food and Drug Administration ... of Colorado Anschutz Medical Campus** **Department: Gates Institute** **Job Title: Clinical Trials Operations Manager ** **Position #:00822863 - Requisition… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Manager (CRM) is responsible for the day to day oversight and management of Clinical Trials Office clinical ... activity to ensure compliance with Standard Operating Procedures and Good Clinical Practices. **JOB DUTIES AND RESPONSIBILITIES:** **Oversight of assigned study… 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 ... financial management of clinical trials preferred. Classified Title: Clinical Research Program Manager Role/Level/Range: ACRP/04/MD Starting Salary Range:… more
- Rush University Medical Center (Chicago, IL)
- …while ensuring the protocol is conducted in a high-quality manner. Educates clinical staff and physicians regarding study. Updates clinical staff on study ... while ensuring the protocol is conducted in a high-quality manner. Educates clinical staff and physicians regarding study. Updates clinical staff on study… more
- Children's Hospital Boston (Boston, MA)
- 74507BRJob Posting Title: Clinical Research Manager IDepartment:Medicine-Hematology/OncologyAutoReqId:74507BRStatus:Full-TimeStandard Hours per Week:40 Job ... the Dana-Farber/Boston Children's Cancer and Blood Disorders Center is seeking a clinical research manager . Ground-breaking research within the group focuses on… more
- University of Colorado (Aurora, CO)
- …clinical tasks and job functions. + Performs additional duties as assigned by clinical manager and/or clinical operations director. **20% Team quality ... a regular basis. + Assists in completion of Internal Protocol Amendment Review forms. + Helps with amendment treatment...job functions. + Performs additional duties as assigned by clinical manager and/or clinical operations… more
- University of Pennsylvania (Philadelphia, PA)
- … trial meets expectations and that they are conducted in accordance with the specific clinical protocol as approved by the Sponsor, study team and in accordance ... and resources, and much more. Posted Job Title Project Manager A/B (Penn Infectious Diseases Clinical Research...performance management, and development of key study documents including protocol , consent, and CRFs. The Project Manager … more
- Emory Healthcare/Emory University (Atlanta, GA)
- …health-related or business administration program required and seven (7) years of clinical research experience, with at least four (4) years of Clinical ... DESCRIPTION: + Responsible for directing and managing large and highly complex clinical research groups. + With support from operational leadership, assesses team… more
