For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career tha...
Multi-Specialty Clinical Research Coordinator. Adherence to Protocol Regulations. Scheduling of Clinical Trial Patients. Electronic Data capturing performed for various trials. Administrative Direct Patient Care. Assist Clinical Trial Physician with patient care. Conduct Phlebotomy, EKG’s, Spirometry. Work Remotely. No. Job Type: Full-time. Pay: $13.00 - $23.00 per hour. Expected hours: 40 per week. Benefits. Dental insurance. Health insurance. V...
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career tha...
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career tha...
Position Title. Study Coordinator. Job Family. Exempt. Location. Hybrid, Roslindale. Title of Immediate Supervisor. Eva Schmitt, Associate Director, Aging Brain Center. I. Position Summary. The Aging Brain Center (ABC), based at Marcus Institute for Aging Research, a Harvard Medical School affiliate, is looking for a highly motivated individual to support their dynamic research team. This is an ideal position for an individual who wants to work a...
The Bioethics Critical Care Study Coordinator will have responsibilities to support and assist the Director in administering and monitoring and daily operation of all Bioethics Critical Care research projects. This position will be fully involved in all Bioethics Critical Care studies and clinical trials, and will responsible for educating and training Bioethics Critical Care staff on the Center's studies, protocol and importance. manage mechanis...
Study Coordinator. This is a contract position and requires previous Ophthalmology clinical research experience. . Job Description. Looking to hire an. onsite full time. individual with clinical research experience to act as a. consultant CRC. to support an ongoing. Ophthalmology. clinical trial. This CRC must be experienced in being able to work independently. You will act as one of the main CRC’s for this study. Please note, as the position and...
A pioneer in K-12 education since 2000, Amplify is leading the way in next-generation curriculum and assessment. Our core and supplemental programs in ELA, math, and science engage all students in rigorous learning and inspire them to think deeply, creatively, and for themselves. Our formative assessment products help teachers identify the targeted instruction students need to build a strong foundation in early reading and math. All of our progra...
Details. Open Date. 12/07/2023. Requisition Number. PRN37127B. Job Title. PS Study Coordinator. Working Title. Study Coordinator. Job Grade. D. FLSA Code. Administrative. Patient Sensitive Job Code. Yes. Standard Hours per Week. 40. Full Time or Part Time. Full Time. Shift. Day. Work Schedule Summary. Monday Friday 8am 5pm with some flexibility according to division need for participant enrollment. VP Area. U of U Health - Academics. Departme...
Coordinates technical and administrative details involved in a clinical or research study. Assists the Principal Investigator in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.This position is eligible for a flexible and/or hybrid work schedule.The University of Utah provides a variety of employee benefits, including health care coverage, retirement plans, and paid leave t...
POSITION RESPONSIBILITIES. Assist in planning and monitoring multicenter implementation of projects• Assist in training and education of informatic tools • Assist in outreach and coordination of Community Advisory Board activities• Travel if necessary for site visits and training for projects• Collect and accurately record data and outcomes for research and monitoring• Manage study implementation at Montefiore and other sites• Coordinate efforts ...
The purpose of this position is to facilitate the conduct of oncology clinical trials, including subject and data management, according to federal regulations, Good Clinical Practice, and local and institutional policies. These responsibilities relate to the mission of the UNC/LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard instituti...
