Key Responsibilities:Serve as gastrointestinal cancer clinical expert and medical monitor on key clinical trialsSupport cross-functional collaborations and provide clinical input into safety and regulatory interactionsDevelop key opinion leaders, identify new research opportunities, and support prod...
Time Type:Full timeDepartment:CC033020 Clinical Research OperationsSummary:The Research Supervisor is responsible for managing day-to-day operations of assigned research teams. Plans and manages research-related activities and ensures work is performed according to research protocol as defined per c...
Key Responsibilities:Assist investigators with submission and activation of human subject research to regulatory committeesManage initial study submissions and oversee ongoing regulatory management for assigned teamCollaborate with stakeholders for budget development, Medicare coverage analysis, and...
The Clinical Research Study Coordinator executes and coordinates daily clinical research activities according to GCP and FDA/ICH guidelines; completes and organizes all IRB/Sponsor regulatory documents; ensures IRB approved protocols are implemented and followed; conducts study specific training on ...
A company is looking for a Clinical Research Medical Director specializing in Asthma/Allergy. ...
Level III: Registered Nurse plus Five (5) years clinical research experience AND demonstrated proficiency in study planning/development, research nursing and research patient management. Serves as the general administrator and liaison for the PI, research subjects, human testing compliance, privacy/...
Position will be responsible for the coordination of research subject activities for clinical trials supported by the Translational Research Institute (TRI) Clinical Trial Innovation Unit (CTIU). This position will work independently to manage clinical trial activities under the guidance of a Clinic...
Position will be responsible for the coordination of research subject activities for clinical trials supported by the Translational Research Institute (TRI) Clinical Trial Innovation Unit (CTIU). This position will work independently to manage clinical trial activities under the guidance of a Clinic...
Provides guidance and training to research staff to ensure compliance with rules and regulations associated with the department’s clinical research studies. Collaborates with clinical trial coordinators and leadership to maintain up to date clinical trial documentation and retraining. Provides eRegu...
Level III: Registered Nurse plus Five (5) years clinical research experience AND demonstrated proficiency in study planning/development, research nursing and research patient management. Serves as the general administrator and liaison for the PI, research subjects, human testing compliance, privacy/...
Position will be responsible for the coordination of research subject activities for clinical trials supported by the Translational Research Institute (TRI) Clinical Trial Innovation Unit (CTIU). This position will work independently to manage clinical trial activities under the guidance of a Clinic...
The Clinical Research Study Coordinator executes and coordinates daily clinical research activities according to GCP and FDA/ICH guidelines; completes and organizes all IRB/Sponsor regulatory documents; ensures IRB approved protocols are implemented and followed; conducts study specific training on ...
The Clinical Research Coordinator (CRC) will be responsible for data collection and management of research related activities and manage administrative tasks for specific research projects for the Office of Community Health and Research. Level III CRCs will obtain or maintain a Certified Research Sp...
Plans and manages research-related activities and ensures work is performed according to research protocol as defined per contract, sponsor, organizational standards, and/or Institutional Review Board (IRB) guidelines. Develops work plans used to achieve research goals and performance metrics. Assis...
Springdale, AR 72762 General Purpose The Clinical Research Coordinator is responsible for following the subjects enrolled on their clinical trials in a manner consistent with Good Clinical Practice guidelines, Highlands Oncology Group policies and procedures, and sponsor requirements within the assi...
Works closely with Clinical Trials Office Leadership and research staff (clinical research nurses, research assistants, investigators, statisticians, regulatory specialists, finance, protocol sponsors, etc. Clinical Research Coordinator I- III will be responsible for data collection and management f...
Attends or facilitates meetings and other communications with investigators, research sponsors, other research staff and investigator staff members for the purposes of coordination of services to support assigned research projects. Schedules and performs initial contact with prospective research sub...
The Clinical Research Nurse (CRN) executes and coordinates daily clinical research activities according to GCP and FDA/ICH guidelines; reviews and assists in the selection of Sponsor supported clinical trials; completes and organizes all IRB/Sponsor regulatory documents; negotiates clinical trial bu...
The Director of Clinical Physics and Research manages the Physics and Dosimetry staff. Work closely with research staff on studies requiring radiation oncology participation. In collaboration with the department director and Physics director is responsible for clinical education, training, and compe...
This Clinical Research Financial Analyst is responsible for the financial management of UAMS clinical trials to include thorough and efficient budget development and negotiation during trial start-up, as well as timely and accurate accounting of clinical trial revenue and expenses throughout the cli...