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

The Senior RA's specific duties may include Supervise other study research assistant staff who are involved in the intervention delivery and/or outcome assessment Manage communication, reports and tracking of deliverables for the research funders across both projects Manage the development of case record forms and study databases, in collaboration with biostatistics team

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

TheCTA is responsible forsupporting the Clinical program teams and may assist the teams across multipleclinical studies. The CTA would also participate in broader clinical operationsactivitiesand initiatives such as the development and refinement of new processes. Responsibilities Clinical Study and Program Support ~70% Support clinical study teams in the delivery of key

Supervisor, Immunohematology Reference Lab Job Locations US RI Providence ID 2024 6191 Category Clinical Laboratory Type Regular Full Time Overview In 1979, the Rhode Island Blood Center was established by the hospitals in Rhode Island as a private, not for profit agency to collect, test, and distribute blood products. Today, the Rhode Blood Center is a division of New Yo

1. Develops and fosters effective and trusting relationships with Thought Leaders and identifies and engages other appropriate (allied) HCPs and other stakeholders involved in clinical practice decision making with regards to managing conditions associated with pain, resulting in scientific engagement with a large network of stakeholders involved in affecting care of pati

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Analyze specimens using approved testing procedures. Review and release test results. Follow CLIA, HIPAA, OSH

Laboratory Tech I or II Third Shift Job Locations US RI Providence ID 2024 5987 Category Clinical Laboratory Type Regular Full Time Overview In 1979, the Rhode Island Blood Center was established by the hospitals in Rhode Island as a private, not for profit agency to collect, test, and distribute blood products. Today, the Rhode Blood Center is a division of New York Bloo

Provide expert guidance to healthcare professionals on cleaning, disinfection, and sterilization processes, including best practices, regulatory compliance, and the use of our products. Utilize scientific methods to draw fact based conclusions during testing for design verification or for troubleshooting and problem solving. Collaborate with the director CDS to ensure the

Accurately fills medication orders under direction of a pharmacist Reviews and ensures accuracy of dosage and medication for each patient Delivers narcotics and stock medications to the units in a timely manner Inspects medication rooms on an ongoing basis, reporting findings monthly Maintains pharmacy inventory at a proper level Returns medications of discharged patients

As it pertains to the service area in the pharmacy department, responsible for the optimization of drug therapy by identification, resolution, and prevention of drug related problems and improving therapeutic outcomes. Responsible for providing direct or indirect patient care according to the laws and regulations governing pharmacists and the practice of pharmacy by the a

Great long term contract opportunity for a Clinical Trial Manager with a local pharmaceutical company in Waltham MA. Looking for 5+ years clinical research experience in a pharmaceutical/biotech, CRO setting. Strong knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials. Will be responsible for the oversight, coordination, and execution of clinic

of Role The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction of the manufacturing manager and on the floor guidance of the team lead, the manufacturing technician II will become qualified and independently capable

1. Professional and Technical Competence 1.1 Communicates well with pharmacy staff on pharmacy issues, and responds appropriately to problem situations. 2. Maintains Appropriate Inventory Levels 2.1 Orders medications and other supplies from vendors as needed. 3. Controlled Substance Inventory and Record Keeping 3.1 Verifies daily controlled substance count in Pyxis durin

Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position. Collects & organizes patient data Maintains records and databases Assists with recruiting patients for