- Eisai, Inc (Los Angeles, CA)
- …confidence in discussing drug information/ disease state management. Prior experience in clinical research , drug development and/or clinical pharmacy ... MSL , 8+ years of overall experience in Oncology with relevant combination industry/ clinical / research / academia; at least 5 years as an MSL in Oncology… more
- Washington University (St. Louis, MO)
- …Summary Under the direction of a Research Coordinator or PI, participates in clinical research study activities; screens, obtains consent, and enrolls in ... variety of duties involved in the collection, documentation, and reporting of clinical research data. Job Description Primary Duties & Responsibilities:… more
- Atlantic Health System (Morristown, NJ)
- …files. Documents subject progress according to good clinical practices in research records. Maintains study drug /device accountability records as ... events per regulatory requirements, sponsor requirements and policies and procedures. Writes study drug prescriptions for trial subjects in accordance with… more
- Merck & Co. (North Wales, PA)
- …Material(s):n/aRequired Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research , Clinical Study Design, ... team, country teams, vendors, committees) in support of clinical study objectives.Accountable for managing any ... specific partners and/or vendors.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and… more
- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability ... PowerPoint, Word, Outlook, etc.)Education/ExperienceBachelor's Degree +9 years of pharmaceutical, clinical drug development, project management, and/or medical… more
- Merck & Co. (Rahway, NJ)
- … to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal ... biomedical research experience in academiaDemonstrated success in overseeing clinical studies and protocolsDemonstrated record of scientific scholarship and… more
- Saint Louis University (St. Louis, MO)
- …JOB SUMMARY Under the direction of the Principal Investigator or designee, the Nephrology Clinical Research Nurse I is responsible to carry out all delegated ... tasks related to complex protocols testing investigational drugs, devices, or research interventions. The Clinical Research Nurse I is aa member of the team… more
- Northwestern University (Chicago, IL)
- …: Technical: Plans, develops & implements new processes & protocols to support research studies & maximize/extend study capabilities. Oversees completion of ... data. Job Summary: Manages all activities associated with biomedical &/or social-behavioral research studies considered very complex by the inclusion of several… more
- Hackensack Meridian Health (Paramus, NJ)
- …with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and ... . Reviews study with principal investigator and/or clinical research nurses to a budget outlining...attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. Collaborates with… more
- Cedars Sinai (West Hollywood, CA)
- …To learn more, please visit: MIRIAD IBD Biobank & Database | Cedars-Sinai. The Clinical Research Associate I works under the direction of a Clinical ... supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies . Supports objectives of research studies… more
- Loyola University Chicago (Chicago, IL)
- Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR II Position Number 8150021 Job Category University Staff Job Type Full-Time FLSA Status ... Is this split and/or fully grant funded? Yes Duties and Responsibilities The Clinical Research Coordinator II is responsible for the overall management and… more
- Eli Lilly and Company (Indianapolis, IN)
- …of clinical trial data in Clinical Trial Registry activities. Clinical Planning Collaborate with Clinical Research Scientists (CRSs), regional ... to investigators and site personnel. Serve as resource to clinical research site monitors, investigators and ethical...as requested Contribute to global alignment of Phase 3b/4 clinical studies (and Phase I and II… more
- Mount Sinai Hospital (New York, NY)
- … Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ... work laboratory, other vendors, and CROs; consultant agreements; investigative device/ drug labels; clinical study worksheets;...Clinical Research . Experience in Phase I-IV clinical studies as a clinical … more
- Baylor Scott & White Healthcare (Plano, TX)
- …mechanisms are in place for research charges related to research studies . Requires familiarity with research study budgets and provides feedback on ... JOB SUMMARY The Clinical Research Coordinator 1 assists various...study -monitoring visits. Conducts audits and quality checks of research studies to check the accuracy, integrity… more
- Merck & Co. (North Wales, PA)
- …with the Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets.Supports ... of country specific HTA/reimbursement needs for the product and gain input on research design and implementation of retrospective database studies , assessment of… more
- Cedars Sinai (Los Angeles, CA)
- … Research Program Administrator or Research Nurse to coordinate/implement study . Evaluates and abstracts clinical research data from source ... investigators continue to advance the field with groundbreaking, life-saving research . From genetic counseling and targeted drug ...Are you ready to be a part of breakthrough research ? The Clinical Research Associate… more
- The University of Chicago (Chicago, IL)
- …on data collected. Oversees and participates in the coordination and conduct of complex clinical research studies and ensures compliance with federal and ... studies . Assists with or plans and implements the clinical study 's goals and objectives; organizes patient... studies to coordinate the collection of analyzable clinical research data and/or samples with a… more
- Sanofi (Cambridge, MA)
- Job Title: Clinical Research Director, I and I, IBD...studies and to create an abbreviated and full clinical study protocol Oversee the execution of ... be critical in helping our teams accelerate progress. The Clinical Research Director (CRD), Immunology & Inflammation...the CDP through internal management review Leads a clinical subteam to design clinical … more
- Washington University (St. Louis, MO)
- Scheduled Hours 40 Position Summary Oversees and coordinates complex or multi-site clinical research studies ; serves as a resource to provide comprehensive ... and performs all duties associated with the coordination and implementation of clinical research study /projects, data collection, and the management… more
- Cedars Sinai (Beverly Hills, CA)
- Job Description Come join our team! The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for ... patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug . Maintains accurate source documents related to all … more
Related Job Searches:
Clinical,
Clinical Research,
Clinical Research Drug,
Drug,
Research,
Research Drug,
Study,
Study Drug