01/07 | Primary Role: Manage experienced data management staff (2 to 4). Provide functional line management for multiple projects and programs. Participate in cross-functional team and committee meetings, as needed, and serve as an escalation point for troubleshooting and resolving issues. Responsibilities: % of Time / Job Duty and Description 5% Participate in the evaluation, integration, and implementat | | Lexington, MA, 0... | | map | | | action |
02/09 | Outcome is seeking an experienced Clinical Data Manager to join the Data Management department to assist with meeting Outcome’s data management needs by m anaging database development and data review for clinical trials and patient registry programs in compliance with standard operating procedures, client guidelines, contractual obligations and regulatory agency guidelines Responsibilities : Revie | | Cambridge, MA, 0... | | map | | | action |
02/03 | For over 25 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and me | | Lowell, MA, 0185... | | map | | | action |
01/19 | RESPONSIBILITIES: • The main responsibility of this position is to manage the data management tasks requested by clients. Candidate must be able to take a clinical trial from beginning to end. • Develop data management plans including required supporting documentation. Manage development of the specification documents for database tables, data entry screens, data derivations and edit check program | | Boston, MA | | map | | | action |
01/20 | Chiltern International is a well established global contract research organization with offices throughout Europe, North America and India. We were established in 1982 and have served pharmaceutical, biotechnology, and device companies in over 38 countries worldwide. Due to our continued growth, Chiltern is seeking a highly motivated individual to join us as a Senior Clinical Research Associate wo | | Cambridge, MA, 0... | | map | | | action |
02/09 | Description: General Summary/Overview Statement The Clinical Lab Systems Analyst Intern position is a beginner analyst position that will assist with key system and business analyst activities primarily focused around the clinical lab and research lab at Dana-Farber. S/he will participate in both projects and system support/maintenance for the labs. Under the guidance of the Clinical Lab Systems T | | Boston, MA, 0211... | | map | | | action |
02/09 | Description: In collaboration with Director of Patient Safety and Quality and other NSPG administrative staff, the Clinical Best Practice Program Manager is responsible for the management and administration of the Medical Assistant training program supported by the Partners Community Healthcare Primary Care Redesign Grant. The Clinical Best Practice Program Manager will develop and implement a pro | | Salem, MA, 01970 | | map | | | action |
02/08 | The Clinical Research Administrator will be responsible for the following tasks: Research Coordination and Implementation: • For research projects, set up, plan, and implement each new study. For some studies, these and steps list below will require collaboration and coordination with co-investigators. • For project start-up, work with the Program Director to develop and refine research designs an | | Boston, MA, 0221... | | map | | | action |
02/05 | The goals of the Clinical Science lab are to understand fundamental mechanisms of engraftment of stem and progenitor cells into lung, and the effect of therapeutic delivery of cells on organ (lung) repair and regeneration. Ultimately, this research will be translated into therapies for chronic lung diseases such as emphysema and pulmonary fibrosis using stem/progenitor cells. The lab is NIH funded | | Grafton, MA, 015... | | map | | | action |
02/05 | New England Rehabilitation Hospital, A Five Star Quality Care Hospital - 2 Rehabilitation Way, Woburn, MA 01801 At New England Rehabilitation Hospital, we recognize that when it comes to healthcare, it is the people providing that care who make the difference. Since it’s establishment in 1969, we have enjoyed a distinguished reputation as the area’s premier provider of physical rehabilitation serv | | Woburn, MA, 0180... | | map | | | action |
02/05 | Job Description: Sr. Developer - Clinical Systems Summary: This position is responsible for implementation of database management activities in support of clinical trials, including: development of programs to generate data tables, listings and reports in support of clinical trial management or departmental initiatives; assist with design and maintenance of clinical study databases using Medidata R | | Marlborough, MA,... | | map | | | action |
02/04 | With minimal direction, the Senior Clinical Project Manager is responsible for management of all clinical aspects of domestic and international clinical trials to ensure compliance with the Clinical Protocol, Standard Operating Procedures (SOP’s), Good Clinical Practices (GCPs) and other applicable regulations. The Senior Clinical Project Manager will: -Manage multiple clinical trials within a the | | Hopkinton, MA, 0... | | map | | | action |
02/04 | Our Lowell, MA based client is seeking an experienced Clinical Logistics Assistant to perform a variety of activities related to Logistics Services such as document and material management, shipment control, or data management to meet the company's standards of quality, customer service, safety, productivity and confidentiality. Key Accountabilities: Provides assistance to Clinical/Technical Logis | | Lowell, MA | | map | | | action |
02/04 | Description: Partners HealthCare offers paid 12-week summer internships in the Information Systems department. This is an excellent opportunity to acquire IT experience while contributing to a leading healthcare organization. The Clinical Informatics Research and Development (CIRD) group's mission is to improve the quality and efficiency of care for patients at Partners HealthCare System by assuri | | Wellesley, MA, 0... | | map | | | action |
02/02 | Medical Writer with Clinical / Regulatory Documentation Experience (Partial Telecommute) Keywords: documentation specialist, clinical writer, clinical data writer, AMWA, project manager, regulatory documents, regulatory medical writer, regulatory writer, regulatory documentation, clinical documentation, medical writing, IBs, CSRs, We are working with our client in locating 2 Medical Writers to wri | | Boston, MA | | map | | | action |
02/02 | The Assistant Director of Clinical Services is responsible for assisting in the implementation of the Melmark Ne w England Behavior Intervention Strategies: Policies and Procedures. This role will assist in the development of all clinical services within the school and residential settings. In addition, the Assistant Director of Clinical Services will ensure that all requirements are met for manag | | Andover, MA, 018... | | map | | | action |
01/29 | The main objective of the position is to implement agreed upon -strategies for the management of clinical projects with pre-specified timelines and budgets. The CPM leads the project team and is responsible for the successful conduct and completion of the project to the contracted budge and timelines and for ensuring the quality of the project according to ICH/GCP, Averion and/or Sponsor SOPs, gui | | SOUTHBOROUGH, MA... | | map | | | action |
01/29 | **Positions can be regional or office based** With minimal supervision, the CRA II performs clinical monitoring activities to assure site compliance with study protocols and GCP. ESSENTIAL DUTIES AND RESPONSIBILITIES INCLUDE THE FOLLOWING: • Independently performs monitoring visits, including Pre-Study, Study Site Initiation, routine/interim Monitoring and Study Site Closure visits in accordance t | | SOUTHBOROUGH, MA... | | map | | | action |
01/29 | POSITION SUMMARY Plans and manages clinical operations for assigned clinical project(s) including timelines, budgets, personnel resources, investigational sites, vendors and key project deliverables; manages, mentors and provides professional development guidance to assigned clinical operations staff members<br/><br/>DUTIES & RESPONSIBILITIES <br/>-Provides strategic planning expertise, drafts the | | CAMBRIDGE, MA, 0... | | map | | | action |
01/29 | Chiltern International is a well established global contract research organization with offices throughout Europe, North America and India. We were established in 1982 and have served pharmaceutical, biotechnology, and device companies in over 38 countries worldwide. Due to our continued growth, Chiltern is seeking a highly motivated individual to join us as a Senior Clinical Research Associate wo | | Cambridge, MA | | map | | | action |
01/29 | Thoughtful Science. Tailored Solutions. NERI is a full-service Contract Research Organization that provides customized, global clinical trial solutions and registry services to pharmaceutical, biotechnology, biomaterial, and medical device companies. NERI also has notable experience collaborating on federally-funded research with organizations like the National Institutes of Health. Since its foun | | Watertown, MA, 0... | | map | | | action |
01/28 | -Works with the Manager, Clinical Operations, the Clinical Research Manager II and other members of the clinical project team to ensure the execution of assigned clinical trials in accordance with Clinical Operations Plans<br/><br/>-Trains and provides oversight to CRA teams including TCR and trip report review, co-monitoring and mentoring<br/> -Convenes and leads the cross-functional, matrix clin | | CAMBRIDGE, MA, 0... | | map | | | action |
01/27 | Chiltern International is a well established global contract research organization with offices throughout Europe, North America and India. We were established in 1982 and have served pharmaceutical, biotechnology, and device companies in over 38 countries worldwide. Due to our continued growth, Chiltern is seeking a highly motivated individual to join us as a Senior Clinical Research Associate wo | | Cambridge, MA, 0... | | map | | | action |
01/25 | Primary Role: Responsible for assisting and providing support to the members of the clinical project team (i.e. Clinical Research Associates and Project Managers) with planning and implementing clinical research projects; and evaluating and analyzing clinical data. The Clinical Trials Coordinator (CTC) is responsible for providing daily support to the Clinical Project Managers in all aspects of cl | | Lexington, MA, 0... | | map | | | action |
01/21 | Primary Role: Responsible for assisting and providing support to the members of the clinical project team (i.e. Clinical Research Associates and Project Managers) with planning and implementing clinical research projects; and evaluating and analyzing clinical data. The Clinical Trials Coordinator (CTC) is responsible for providing daily support to the Clinical Project Managers in all aspects of cl | | Lexington, MA, 0... | | map | | | action |