Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for complex research protocols related to treatment, a

1. Competent in the Practice of Pharmacy 1.1 Does not have high error rate when entering orders, making IV medications or checking the Pyxis refill. 2. Controlled Substances Inventory and Record Keeping 2.1 Dispenses narcotics/controlled substances according to hospital policy. 3. Sterile Product Preparation 3.1 Complies 100% of time with required clean room attire and cl

Data entry of test orders, presort, pickup and delivery of processed specimens to the laboratory, centrifugation and aliquoting Process specimens to be sent out to additional facilities Prepare laboratory specimens for various analysis and testing Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands the

Data entry of test orders, presort, pickup and delivery of processed specimens to the laboratory, centrifugation and aliquoting Process specimens to be sent out to additional facilities Prepare laboratory specimens for various analysis and testing Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands the

We're offering a generous sign on bonus ($10,000) to welcome you to our team. Recognizing and valuing exceptional talent, we're eager to discuss the exciting details of this bonus during our interview process. Monday Friday evenings 3 00 pm 11 30 pm and rotating weekends and Holidays. BLOOD BANK TECHNOLOGIST A highly regulated environment (AABB, CAP, TJC, DPH, CMS), perfo

Data entry of test orders, presort, pickup and delivery of processed specimens to the laboratory, centrifugation and aliquoting Process specimens to be sent out to additional facilities Prepare laboratory specimens for various analysis and testing Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands the

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator I is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary

of Key Responsibilities Develop, implement, and oversee Alnylam's Clinical Trial Oversight strategy in alignment with ICH GCP E6 and E8 Lead, direct, and support Clinical Trial Oversight Leads (CTOLs) in assessing CRO monitoring effectiveness across the portfolio Direct day to day work activities for FSP vendor for Clinical Trial Oversight Consistently manage oversight act

Lead and manage integration of all project team activities, leveraging internal and development partner resources, expertise and knowledge, along with optimizing CRO resources, expertise and knowledge. Provide strategic input and execution of clinical trials from protocol design to the final clinical study report for specified studies Provide leadership and input into glo

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion, talented peers, c

Cath Lab Tech Facility Landmark Medical Center Location US RI Woonsocket ID 2024 158637 Category Clinical Tech Position Type Full Time Shift Days Job Type Non Exempt Overview At Landmark Medical Center, our dedicated team of professionals is committed to our core values of quality, compassion, and community. As a member of Prime Healthcare, Landmark Medical Center is acti

Aya Healthcare has an immediate opening for the following position Clinical Research Coordinator in Boston, MA. This is a 26 week contract position that requires at least one year of Clinical Research Coordinator experience. Make $3412.9/week $3570.9/week. Want a job close to home? We've got you! We'll work with you to build the career of your dreams. Aya delivers Front o

The responsibilities of the clinical research coordinator may include but are not limited to the following activities Screening, obtaining informed consent, and enrolling study participants. Maintain enrollment reports. Prepare study mailings Organizing and participating in study related meetings and study site visits. Prepare meeting agendas and minutes when applicable C

Responsible for the development and completion of the resident assessment and care planning in accordance with state and federal requirements, and policies and procedures of the facility. Required Skills Current, valid, and active license to practice as a Registered Nurse in the state of employment required. Three (3) years of experience in a healthcare setting required.

1. PATIENT SAFETY Follows established hospital and departmental precautions and procedures in the performance of all job duties to ensure a safe work environment for patients and others to include as appropriate Demonstrates appropriate hand hygiene Demonstrates use of two patient identifiers Demonstrates effective communication "hand offs" between providers, shifts, depa