Research Coordinator Salary at Semel Institute For Neuroscience BETA

Job Description Job Description Job Summary We are seeking a motivated and detail-oriented Research Coordinator to join our team. The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies. Responsibilities · Provide clinical research support to investigators to prepare for and execute assigned research studies, including: · Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data; · Attend all relevant study meetings; · Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research; · Recruit and screen patients for clinical trials and maintain subject screening logs; · Orient research subjects to the study, including the purpose of the study, p

Job Title Research Coordinator Job Description Summary The Data Specialist reports to the Local Manager. The Data Specialist is responsible for supporting the development of local research output and data collection. Specifically, this position provides support for gathering and entering local market data into Cushman & Wakefield's proprietary database. The Data Specialist is accountable for accurate and proactive maintenance of proprietary and third-party databases with local market data, as well as pulling data from said systems to support the business's needs. This position is not specific to a service line but may specialize by property type. Job Description Responsibilities: Perform primary research on buildings that are built, under construction, proposed or under renovation Call and/or inquire on available properties, update proprietary database as applicable Track new construction, renovations, and completions, leases and sales, tenant movements (tenants in the market), direct

Essential Duties and Responsibilities: Recruit subjects for research Provides programmatic, data management, and research study support. Assists community program staff and clinical partner organizations coordinate a study of a patient education course and related research activities. Conducts literature reviews, carries out educational health intervention protocols. Assists with computer aided survey implementation and supports human subjects protection documentation and reporting. Facilitates interviews and meetings for project activities. Ensures intervention logistics are implemented properly. Assists in the collection and management of project related data. Provides support preparing educational and dissemination materials for clinical providers, health administrators, and lay persons. Aids in developing Standard Operating Procedures. Serves as liaison for key function areas including interfacing with clinics and hospitals, Health Information Technology and Bio-medical Informatics

Job Description Job Description National Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a Clinical Research Coordinator with 2 or more years of experience. Duties for this position will include managing the study from placement to completion of the final study report. The CRC is responsible for the conduct of quality and efficient clinical trials. REQUIREMENTS: A minimum of 2 years of clinical research experience is preferred. In-depth knowledge of the clinical research process, including Good Clinical Practices and ICH guidelines; Strong interpersonal and communication skills; excellent attention to detail; exceptional organizational and planning skills. Able to project and coordinate study needs in advance. Candidate needs to have good troubleshooting and conflict-resolution skills. Being bilingual in English/Spanish is a plus! NICR is an independent, multi-site clinical trial management organization (SMO).

Clinical Research Coordinator Great opportunity to work with a big name sponsor on an Ophthalmology study 100% ON SITE Position Summary: The candidate will be coordinating clinical research protocols from study start up to close out. This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices. Responsibilities: May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO Participates in the identification of potential clinical trial participants, screens them for eligibility, Coordinates the schedule of events for clinical trial participants from screening to follow up according to protocol Collects, verifies, organizes and records clinical information and data in elec

Responsibilities/ Job Duties: Contract clinical research coordinator assignment coordinating complex ophthalmology trials. Employee will assist with Study Visits, sample collection and processing - excluding venipuncture and study drug administration - audit preparation, monitoring visits, consenting, query resolution, data entry and data migration, AE monitoring, prescreening for eligibility, as well as scheduling appointments and sending appointment reminders. Minimum Education and Experience Qualification Requirements: Minimum 2 years clinical trial coordination experience Experience with EDC data entry/management, query resolution required Experience with study visit management including screening, enrollment, consenting, etc. required Experience managing regulatory documentation including managing regulatory binders required Ophthalmology experience preferred Bachelors degree preferred Schedule/ Shift: Full time (40 hours a week), M-F, between 8-5 Benefits (full time only): Paid S

Responsibilities/ Job Duties: This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices. Responsibilities - May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO Collects, verifies, organizes and records clinical information and data in electronic data capture systems EDC. Abstracts data from necessary sources to complete the EDC and resolve queries. Performs the following data related activities: EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding Minimum Education and Experience Qualification Requirements: Minimum 1 year experience with clinical trial coordination required Minimum 1 year EDC data entry

TITLE: Clinical Research Coordinator RN LOCATION: Newport Beach, CA (Onsite) SCHEDULE: 8:30 AM – 5 PM PAY: $99K - $152K Annual DOE This is the pay range that BAHAMA Consulting reasonably expects to pay someone for this position. SUMMARY: The Clinical Research Coordinator RN - Start-Up will support and participate in the overall startup activities for the Center for Clinical Research within the hospital. Provides support and coordination for FDA regulated research including drug/device/biologic studies that may involve industry-sponsored Phase I, II, III and IV clinical trials, government funded clinical research and investigator initiated clinical research. RESPONSIBILITIES: This role will help support clinical start-up activities by ensuring timelines for study activation are met. The Clinical Research Coordinator RN – Start-up will participate in the study feasibility process working closely with department leaders to assess operational and financial feasibility. This will include th