Responsibilities: Collect, enter, and manage clinical trial data using electronic data capture (EDC) systems... in collaboration with clinical staff. Generate data listings and summaries for interim and final study reports. Ensure data handling...
Description & Requirements Maximus is seeking a Clinical Assessment Coordinator to support the Iowa PASRR program... appropriate level of care and services. The Clinical Assessment Coordinator serves as a key point of contact, supporting assessors...
. Responsible for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously... completed. Qualifications Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience...
POSITION SUMMARY: The Nursing Clinical Coordinator is responsible for coordinating clinical activities, ensuring high...-quality patient care, and supporting the orthopedic staff in their clinical practices. The role is focused on ensuring the...
6-12 Month Project - Hybrid in Boston / 4x per week as needed with patients $30/HR W2 Clinical Research Coordinator... appropriate EMR and eCRF systems Maintaining on-going communications with research managers and PIs for data collection needs...
supervision of the Program Director, this Clinical Administrative Coordinator position is responsible for providing technical... and administrative support for clinical year operations of the Tufts Physician Assistant Program. The Physician Assistant Program...
Investigator for assigned research studies, the Clinical Research Coordinator II (CRC-II) is an experienced-level position... projects, and CH-CRP patient and community engagement efforts. Position: Clinical Research Coordinator II, Cancer...
Investigator for assigned research studies, the Clinical Research Coordinator II (CRC-II) is an experienced-level position... projects, and CH-CRP patient and community engagement efforts. Position: Clinical Research Coordinator II, Cancer...
Investigator for assigned research studies, the Clinical Research Coordinator II (CRC-II) is an experienced-level position... projects, and CH-CRP patient and community engagement efforts. Position: Clinical Research Coordinator II, Cancer...
. Responsible for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously... completed. Qualifications Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience...
, the Clinical Research Coordinator (CRC) will perform research activities using approved techniques. The CRC procures..., maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks...
POSITION SUMMARY: The Clinical Coordinator, Controlled Substances is responsible for controlled substances management... across the hospital and affiliated clinics. The Clinical Coordinator will ensure our policies and procedures meet all federal...
more about Care Access, visit . How This Role Makes A Difference The Travel Clinical Research Coordinator primary responsibilities...' decentralized clinical research process, the Travel Clinical Coordinator will be able to assume a greater study workload, overall...
, data management, and methodological support in the development of clinical research protocols and data management tools..., data management, and methodological support to PIs in the development of clinical research protocols and data management...
General Summary: This position will assist the Principal Investigator (PI) in planning and implementing clinical... spans federally funded (NIH) grants, foundation-supported initiatives, and industry-sponsored clinical trials, reflecting...
Job Overview This position will assist the Principal Investigator (PI) in planning and implementing clinical research.... Monitors the occurrence of clinical adverse events, reporting any to the (PI), the study sponsor and Institutional Review Board...
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific... Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management...
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific... Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management...
protocol implementation, completing required forms, reporting results and regulatory submission. Creates study-specific data... collection and statistical and analytical reports. Responsible for managing and coordinating the clinical studies as members...
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific... Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management...