- Spaulding Rehabilitation (Charlestown, MA)
- Clinical Documentation Integrity Specialist , Per Diem - ( 3303241 ) **Description** **Job Summary** Under the direction of the Clinical ... as applicable * Educates physicians and key healthcare providers regarding clinical documentation integrity and the need for accurate and complete … more
- Tufts Medicine (Burlington, MA)
- **Job Profile Summary** The role of the Clinical Documentation Integrity (CDI) Specialist III is responsible for concurrent and retrospect review and ... leadership in an acute-care hospital setting 4. Four years' experience in Clinical Documentation Improvement/ Integrity 5. Advanced clinical expertise and… more
- PaxeraHealth (Newton Center, MA)
- …Radiology Technologist experience to join our talented team of individuals as Clinical Applications Specialist . We seek a talented and qualified professional ... who will embrace our culture of excellence, service and integrity . This person will perform perform pre/post-sales presentations, training and support of our… more
- Merck (Boston, MA)
- …(Bulk Drug Product and Clinical Finished Goods). + Responsible for authoring clinical supply documentation in support of labeling and packaging activities as ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...well as supply chain documentation to support critical CMC activities. + Responsible for… more
- Center for Life Management (Derry, NH)
- …to stabilize a psychiatric crisis and initiate immediate treatment. The Peer Specialist on this multi-disciplinary team will transform our mental health system and ... by supervisor; + Function professionally and in a manner that protects the integrity , confidentiality and rights of all patients; + Execute all required services and… more
- Kelly Services (Cambridge, MA)
- Kelly Science is seeking a Principal QA Validation Specialist for a growing company located in Cambridge, MA. ** This position would be alternating between working ... Employment Type: 6+ month contract Summary: As the Principal QA Validation Specialist , you will be responsible for will be responsible for providing expertise… more
- Tufts Medicine (Tyngsboro, MA)
- …or a role that focuses on support of daily business activities (eg, technical, clinical , non- clinical ) operating in a "hands on" environment. The majority of ... the delivery of support services or activities, typically under supervision. A specialist level role that requires very advanced knowledge of operational procedures… more
- Bristol Myers Squibb (Devens, MA)
- …and other GMP processes as required. Performs review and approval of documentation associated with in-process materials, and manufactured product. Assists in the ... readiness walkthroughs per procedures as needed. + Assures all electronic and paper documentation , which requires QA review is in compliance with corporate and site… more
- Bristol Myers Squibb (Devens, MA)
- …to end user. + Create, deploy, and sustain of electronic systems documentation and Master Data. + Perform project, CAPA and deviation/ investigation related ... and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability,… more
- Capgemini (Boston, MA)
- **Job Description:** We are looking for a dedicated Veeva Clinical Operations Specialist to support the management and execution of clinical trials using the ... Vault Clinical platform. The ideal candidate will have experience in clinical operations, strong knowledge of clinical trial processes, and hands-on… more
- HealthEdge Software Inc (Boston, MA)
- **Overview** **Position Overview:** We are seeking a Senior Payment Integrity Specialist to play a key role in building and implementing proprietary healthcare ... the industry narrative, providing a more holistic approach to payment integrity that focuses on comprehensive reimbursement, agile editing, and integrated analytics.… more
- ThermoFisher Scientific (Waltham, MA)
- …step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel ... frameworks for clinical research through our PPD clinical research...to assess protocol and regulatory compliance and manages required documentation . Manages procedures and guidelines from different sponsors and/or… more
- Center for Life Management (Salem, NH)
- …beyond the immediate amelioration of the acute episode; + Provide timely documentation on each service delivered; + Engage in appropriate consultation meetings and ... by supervisor; + Function professionally and in a manner that protects the integrity , confidentiality and rights of all guests; + Execute all required services and… more
- Microsoft Corporation (Burlington, MA)
- …staff, and patients. We are looking to hire a Senior Medical Device Specialist , with a technical background and a customer-driven passion for regulatory work, to ... Each day we build on our values of respect, integrity , and accountability to create a culture of inclusion...of the Quality Management System (QMS) + Authors technical documentation , and designs and implements Medical Device validation protocols… more