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clinical research in Boston

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  1. Clinical Operations Data Specialist

    Hello,   My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Clinical Operations Data Specialist position for a prominent client of ours.  This position is located in Cambridge, MA. Details for the positions are as follows:   Job Description:   Job Purpose       Experienced clinical operations team member with a special focus in clinical aspects of data cleaning and data trend identification.  Could also include other aspects of ...

  2. Lupus Program Manager

    Our client is a Boston based company that employs a novel approach to systems biology and utilizes systems engineering and bioinformatics modules to cross-validate biological output. They are currently seeking a Lupus Program Manager for this location. Our client is initiated extensive collaborative and research agreements (CRADA) with academic & government organizations and is actively recruiting a Program Manager to oversee the implementation of one of the on-going projects on both research and ...

  3. (2) Technical Lab Services - Technologist (3427314)

    Duties and Responsibilities: 1. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result; 2. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; 3. Analyze specimens using approved testing procedures (see department SOPs). 4. Review and release test results. 5. Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective ...

  4. $5K Sign On Bonus- CRA  Monitors Needed - Set Yourself Up for Success

    CRAs - Join Covance and receive a $5000 Sign On Bonus! Meet the CRA hiring team at the ACRP conference - email [email removed].   Set yourself up for SUCCESS with Early Clinical Development! Now is the time to join our growing business where you have supportive management and a cohesive team. At Covance, you are not just a number. We value you and your hard work...we want you to succeed.   URGENT Need for Oncology Monitors! Calling all Experienced Clinical Research Associates / CRAs / Monitors ...

  5. Health Information Coding Manager

    Sidra’s Health Information Management Department ensures information management standards are consistently applied across systems to maintain the level of data integrity, quality, and privacy necessary for clinical, demographic, financial, evidentiary and administrative data to facilitate real-time healthcare deliver. Responsible for planning, organizing, directing and controls day-to-day operations in the HIM Coding department. Collaborates with and educates clinical staff on coding and ...

  6. FT EM Pediatric Opportunity Qatar (Doha)

    Facility: Sidra Medical & Research Center Opportunity: FT ED Pediatric Physician 400-bed Facility Sidra is part of a dynamic research and education environment in Qatar that includes leading international institutions, such as Sidra’s academic partner Weill Cornell Medical College in Qatar, and Qatar Science and Technology Park. At its core, Sidra will have a unique working structure with inter-professional collaboration, providing the best holistic care for patients and an unparalleled learning ...

  7. Director of Health Information Management

    Sidra’s Health Information Management Department ensures information management standards are consistently applied across systems to maintain the level of data integrity, quality, and privacy necessary for clinical, demographic, financial, evidentiary and administrative data to facilitate real-time healthcare delivery. The Director-Health Information Management (HIM) is responsible for leading and directing health information management services across the multi-facility academic healthcare ...

  8. Quality and Improvement Lead

    The Quality and Improvement Lead is responsible for the implementation and ongoing development of the NSQIP Program within the Department of Surgery. The QI Lead will collaborate with all stakeholders, especially IT to ensure a robust infrastructure is established that allows for concise data extraction, report analysis and a robust interaction with medical records. Crucial to the success of the program is the development of program related policies and procedures coupled with the ability to identify ...

  9. Supervisor of Occupational Therapy

    The Supervisor of Occupational Therapy will be responsible for leading and demonstrating the provision of safe patient and family focused quality care. The Supervisor of Occupational Therapy is a key member of the inter-professional team and ensures that standards for occupational therapy care are adhered to at service level as well as works collaboratively with the Manager of Occupational Therapy to ensure commissioning, recruitment, on-boarding, orientation and service activation responsibilities ...

  10. Bereavement and Palliative Care Manager

    The Bereavement and Palliative Care Manager will lead and demonstrate the provision of patient and family focused support service 24 hours a day. The Bereavement and Palliative Care Manager is a key member of the interprofessional team and ensures that standards for care and compassion are adhered to at the service level. In collaboration with team members, the Bereavement and Palliative Care Manager is accountable for ensuring that commissioning, recruitment, onboarding, orientation and service ...

  11. Physical Therapy Manager

    They Physical Therapy Manager will be responsible for leadership in the areas of operations, administrative functions and collaboration with clinical programs as well as promote a culture of continuous improvement and help generate innovative ideas within Rehabilitation. The Physical Therapy Manager will develop programs and program evaluations, research activities and evidence based practices, facilitate education programs and perform other duties as delegated by the Director of Physical Medicine ...

  12. Nurse Practitioner

    We are seeking Family Nurse Practitioners (FNP), Pediatric Nurse Practitioners (PNP), Neonatal Nurse Practitioners (NNP) and Emergency Nurse Practitioners (ENP). The Advanced Practice Nurse is a licensed independent practitioner who is responsible for managing health problems and coordinating age appropriate health care for the patient. S/he is part of the innovative care team that will meet the individual needs of the patient and their family. The Advanced Practice Nurse practices in accordance ...

  13. Medical Director, Medical Affairs

    Medical Director, Medical Affairs Location: Cambridge, MA (local candidates or those within the NE preferred) Position Type: Full-Time/Regular Our Client is a growing Biotechnology Company exploring targeted therapies for cancer. The Company seeks a Medical Director who is highly motivated to make key contributions to Medical Affairs Research and Communications.  The successful candidate will actively lead and participate in a broad range of Medical Affairs activities including, but not limited to ...

  14. Medical Accounts Receivable Specialist

    Immediate opening for exceptional medical billing professionals who are looking to join our expanding and dynamic healthcare company We are interested in candidates that possess a can do attitude and would enjoy our fast paced, high-level, energetic, team-minded Revenue cycle department: Processing electronic claims Insurance Verification & Follow Up Knowledge & understanding of EOB’s, HCFA & UB04 forms Working Aged Accounts Receivables Analyzing & working claim issues through resolution ...

  15. URGENT NEED!!!   Genetic Counselor

     Judge Healthcare is actively seeking a Genetic Counselor for a growing diagnostics/testing organization in Marlborough, MA. The Genetic Counselor will support testing primarily in the neurogenetics area. This job will have the following responsibilities: · Client consultations and case review · Collection of clinical information necessary to interpret test results and to interpret variants. · Facilitation and coordination of specific samples in the laboratory. · Test verification and management ...

  16. 3952819 – Clinical Trial Leader

    3952819 – Clinical Trial Leader     Responsibilities: Lead the clinical protocol development process in collaboration with the Clinical Program Leader (team MD): responsible author for clinical protocols, amendments and related documents; contribute to the medical/scientific input given for the development of trial-related documents and processes which reside in other line functions; obtain approval from internal review boards. Contribute to the development of clinical sections of regulatory ...

  17. Clinical Study Manager

    Our client, located in Cambridge MA is seeking multiple Clinical Study Managers for permanent opportunities. These positions must work onsite at our client(can work from home 1 day per week). Some relocation provided for candidates with STRONG interest to relocate to the Boston area. Duties and Responsibilities: Manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and SOPs, and supporting clinical strategy defined in ...

  18. Senior Clinical Research Associate (Sr. CRA)

    In-house role.  No travel.  REQUIRED: Required: Bachelor’s in Science/Health Related Field and/or BA Preferred: Masters or Nursing Degree; certification as Clinical Research Associate and/or Clinical Research Professional 5+ years of Clinical Trial experience required in a pharmaceutical, biotech or CRO setting.  3+ years of independent clinical monitoring, including qualification, initiation, interim, and close-out. Clinical trials research experience through exposure to protocols in a variety ...

  19. Biobank Associate Scientist III ( IATA; Pathology Lab experience)

    Title: Associate Scientist III, Technical Development Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Months, possibility converting to FTE Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: The Biobank Associate Scientist III will design and manage all Biobank-relevant aspects of a clinical trial project and investigator-initiated pre-clinical research project as related to biospecimens needing to be collected, processed, labeled, shipped and ...

  20. Biotech Sales

    Cambridge Scientific Products is seeking a salesperson in the field of Biotechnology Research Equipment in the Boston Area.   Requirements: · Possess working knowledge of laboratories (clinical and industrial) through previous work and sales experience · Possesses BA or BS degree in Science, Marketing, or Related Field · 2+ years of sales · Demonstrate ability to work independently · Strong oral and written communication skills · Excellent selling, goal and objective setting skills ...

  21. Senior SQA Manager

      The Senior Manager, Project Software Quality Engineering, is a hands-on leadership role with responsibility in managing all project testing resources and processes for handheld and web-based applications that are deployed globally for clinical research data acquisition and data management. In addition to the responsibilities listed below, this individual will: Initiate and drive ideas to reduce cost, improve quality, and improve efficiency in existing processes or by implementing new processes. ...

  22. Associate Director, Biologics CMC Dossier Development and Coordination

    The CMC Dossier Development and Coordination (CDDC) department within the R&D Scientific Core Platforms (SCP) organization has the broadly defined roles and responsibilities for the development, coordination and delivery of high-quality CMC dossiers in a timely manner for all small and large molecule based pharmaceutical and biopharmaceutical products from First in Human clinical studies to Market Authorization Applications. Examples of CMC dossier deliverables include but are not limited to: o IND ...

  23. C# .NET Developer

    Work / Life Balance! This newly created position is ideal for someone who wants to do interesting work at a prestigious medical research organization and be home in time for dinner each night!  We are seeking a dynamic Sr. Software Engineer (.NET) who will be responsible for the analysis of user needs, software and database design, programming and life cycle development of all business and clinical applications. The successful candidate will work with other engineers in the design and development ...

  24. 3978972 – Clinical Research Documentation Specialist

    The Trial Document Specialist assists with the lifecycle management and associated processes (from study set up to archiving) of Trial Master Files (TMF) for clinical trials   Responsibilities:   Supports Clinical Trial Leaders (CTLs) in the set up of an electronic Trial Master file process for assigned studies Work with document systems and related group to ensure groups are trained on document management systems or other agreed process for electronic TMF document delivery Work with sites to ...