Clinical Research Coordinator II-Pittsburgh Wound Healing Centers. Maintains research practices using Good Clinical Practice (GCP) guidelines. Clinical Research Coordinator II. Conducts research assessments on study participants. ...
Previous experience in study set up / site initiation / study start up experience or equivalent experience in clinical research environment, with understanding of clinical trials methodology and terminology. Initiation Clinical Research Associate. This role involves performing all study start up act...
Scheduling/Appointment Reminders.Minimum Education and Experience Qualification Requirements: .Monday through Friday business hours....
Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure the efficient and compliant clinical operation of the Early Phase Clinical Unit (EPCU). Parexel Early Phase Clinical Unit. You work as part of a team and will collaborate with other departme...
Posted Job TitleClinical Research Nurse B Job Profile Title Clinical Research Nurse BJob Description SummaryThe landmark DCCT study (1983-1993) demonstrated the benefits of intensive therapy aimed at near normal glycemia versus conventional therapy (as practiced in 1982) in reducing the risk of micr...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
We are seeking a problem-solving oriented, “hands-on” strategic solutions leader to head our exceptional Client Services Delivery team, that has a passion for working closely with our business development team to gain credibility with our clients by identifying and recommending innovative ways of de...
The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...
Promote good clinical practice in the conduct of clinical investigations, including possessing and in depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Coordinate and conduct clinical studies, including subject recruit...
The Manager of Clinical Research Operations of the Office of Clinical Research (OCR) will support the Director and VP of Clinical Research by supervising the job functions of Clinical Research Team Leads and Team Lead RNs and CRAs. This role will work with the manager of the Clinical Research Unit o...
Performs a variety of research, data base and clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data. Works under direct supervision and assists research coordinators with organizing, gathering and compiling clinical resear...
Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. Coordinate and facilitate the conduct of clinical research protocols which may be supported by ...
Schedule: varied including evening, overnight, and weekend hours Type: Direct Hire Overview: A top-ranked research university is currently searching for a Clinical Research Coordinator for one of its growing departments to be responsible for assisting in the operations of ongoing clinical trials....
Oncology Clinical Research Nurse. Work closely alongside PI and clinical research coordinators. Minimum of 3 years of Clinical Research Nurse experience. If no Clinical Research Nurse experience, must have a minimum of 1 year of Oncology experience AND 3 years of nursing experience in a clinic setti...
Organize and maintain subject research charts, ensure study documentation is complete and accurate, including provider documentation of study visits in the EMR, collect and enter study data into study databases such as REDCap, PennCTMS, Oracle Clinical, and LabVantage, complete case report forms per...
The CRC-B will work closely with a cross-departmental research team and will be responsible for all phases of study management including: assisting in the development of research materials, maintenance of study records and data, submission of IRB modification and other regulatory documentation, data...
Clinical Manager Research Project A. Clinical Manager Research Project B. Manage single and multi-site clinical trials (including study start up, regulatory submissions, daily operations, external site communications (including DSMB members) and troubleshooting, recruitment and enrollment; QA& QC; S...
The job functions include source documentation generation in startup, maintain DOA log, contacting patients/caregivers to schedule research visits / tracking enrollment progress; Organizing and coordinating research visits; Run the study visit (cog testing, collect/process/ship biosamples, image tes...
Under the direction of the Cancer Center Clinical Trials Office Administrative Director, the Clinical Research Cancer nurse will lead day-to-day operations of clinical research studies conducted by principal investigator(s) at Penn State Cancer Institute Clinical Trials Office. The RN Clinical Resea...
Provide supervision and support for other clinical research coordinators and or/ monitors who are assigned to specific protocols and who will help with the overall clinical research of the program. Applied knowledge of Good Clinical Practice (GCP) guidelines including protection of human research su...
Clinical Research Coordinator- Pool-(24003069). ...
The Research RN will direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. The Research RN will plan, direct, or coordinate clinical research projects. The research nurse may evaluate and analyze clinical data. Exp...
The Clinical Research Coordinator will work under the direct supervision of the Director, CRORA in collaboration with the Principal Investigators to provide research support requiring the application of standard clinical research practices. The Clinical Research Coordinator will be responsible for t...
Job Title: Clinical Research Coordinator II Location: Pittsburgh, 15213 Schedule: M-F 8:30AM-5PM varied, including evening, and weekend hours Hourly rate: $25-$27/hour, Mileage reimbursement for travel to East Palestine, OH Type: 3-6 month Contract Overview: A top-ranked research university is cur...
He or she will perform a preliminary protocol assessment with the Supply Chain Lead (SCL), Clinical Research Pharmacist (CRP) and clinical team members (e. IRT strategy for clinical customer, investigator site, Global Clinical Supply, and ultimately for the patient. Job Title: Interactive Response T...