LAB COORDINATOR , Koch Institute for Integrative Cancer Research Stark Lab , to play a crucial role in facilitating groundbreaking research programs on cancer immunology and immunotherapy by supporting, developing, and contributing to research projects that involve approaches from molecular and synthetic biology, immunology, glycobiology, and biological engineering. Will

Primary Work Address 300 Longwood Avenue, Boston, MA, 02115 Current HHMI Employees, click here to apply via your Workday account. We are always open to finding self motivated and highly organized Lab Manager candidates for potential opportunities within our labs in the greater Boston area. Applications are accepted on a rolling basis. You will be contacted by a member of o

Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon needs. Similarly, not all duties that have been outlined will be assigned to each position. Implementation of research protocols, including collection of 1) surveys and clinical assessments; 2) clinical, cogn

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

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

Clinical Operations Assist PI in development of protocol specific tools to aid in study documentation Collect record, evaluate, update, and store/transport pertinent data and samples in relation to protocol Schedule patient tests and/or interviews Conduct patient telephone follow up Maintain appropriate operations as needed including to stock, inventory, store, and order

Independently author, review, and manage clinical documents as the lead medical writer. Lead strategy discussions for document development and contribute to medical writing process development. Manage contract medical writers. Primary Responsibilities Independently authors high quality, scientifically accurate, complex clinical documents, ensuring consistency between rela

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

improving the quality, cost and experience of health care. Here, we focus on delivering the best patient care, rather than volume. Through innovation and superior care management, we support patients and your well being as a team member. Join a team at the forefront of value based care and discover the meaning behind Caring. Connecting. Growing together. Positions in this

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

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

No direct supervisory responsibilities but may advise the work of others Qualifications High school diploma Bachelor's degree preferred; 5 years of experience preferred. KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED Computer literacy Expert with new applications and software programs. Expertise with Excel/Google Sheets preferred Organization Extensive experience with electron

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 Uses software programs to generate gr

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.