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clinical research in Raleigh

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  1. Associate Project Manager at Cenduit

    E.g., data management, clinical research/operations, etc., a plus. Our interactive response technology (IRT) platform uniquely integrates both patient...

  2. Head of Oncology Center of Excellence - US based at Quintiles Transnational

    In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; Knowledge of clinical research financial parameters and...

  3. Director of Regulatory Affairs at Sterling Hoffman Life Sciences

    Oversee clinical study design and development of clinical protocols. Support execution of Clinical Affairs activities to generate clinical utility/performance...

  4. Business Development Executive- eClinical at ArisGlobal

    The BDE is responsible for identifying, approaching and selling software products to the Life Science Clinical Research domains....

  5. Sr Program Manager Health Economics and Outcomes Research at Medtronic

    7+ years health economics, outcomes research and/or clinical research experience in a medical device or related industry (e.g....

    Ads
    1. Study Start Up Associate ( Contract) - 1510903

      Responsible for the quality and regulatory compliance of Principal Investigator (PI) credentials, Essential Documents  (ED) and Investigator Site Files (ISF) throughout the clinical study.  Work with both internal and external teams to assure good communication, regarding documentation processing.  Assure documents maintained in ISSC are in compliance with International Congress on ...

    2. Clinical Research Coordinator

       Position Description:The primary role of the Clinical Research Coordinator (CCRC) in clinical research is to manage and coordinate the smooth, accurate progress of clinical protocols from the planning stage through study completion by acting as a liaison to the Investigator, the Subject, the Research Center, the IRB, and the Sponsor.  Position is in an active cosmetic surgury center.  Will ...

    3. Clinical Support Associate -  98170

      Title of Position: Clinical Support Associate  Minimum REQUIREMENTS: • Requires undergraduate degree or equivalent in a health or science related discipline. • Demonstrates solid scientific expertise • Possesses working knowledge of Good Clinical Practice (GCP) and other regulations governing clinical research • Demonstrates some drug development experience within the pharmaceutical industry ...

    4. How to Become CLINICAL RESEARCH ASSOCIATE – PROGRAM AWARENESS SESSION

      Subject: How to Become CLINICAL RESEARCH ASSOCIATE – PROGRAM AWARENESS SESSION SATURDAY 1ST AUGUST 2015 @11 AM - US EASTERN TIME ENROLLMENT IS REQUIRED FOR ATTENDANCE.     Dear Candidate, LEARNING's FOR JOB (ONLINE HOME BASED / ON-SITE CLASSES) We are conducting a FREE Awareness session to - "How to become a Clinical Research Associate". Our programs provides most learning's required ...

    5. Director - Clinical Developer - IVD Products

      Seeking individual with clinical development experience to lead diagnostic and therapeutic co-development clinical trials. Shall: *** Lead teams working on companion diagnostic and IVD product development. *** Author and implement clinical development plans and clinical trial protocols. *** Design case report forms, clinical data listing and tables for clinical trial activities. ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    6. Clinical Site Associate (Perm) (Cardiac Device) - 1514773

        Responsible for site management activities, clinical data review, query resolution  management, and collaboration with clinical operation team members and other defined departments  on assigned sites which are participating in Novella clinical trials to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and ...

    7. 98087 – Clinical Project Leader - REMOTE

      This job is 100% remote Must haves: Remote position TA: Metabolism/Diabetes (preferred but not required) Must have project management experience (2+ years), but also like this work, it will be very fast paced to start, working with co-cpls so team collaboration is essential Must have Medical Affairs experience (meaning Phase IV) Need someone who is accountable, takes initiative, ...

    8. Clinical Trials Assistant II

      Job Description Kelly Services has an exciting opportunity for a Clinical Trials Assistant to service a premiere account. The individual will be responsible for providing professional service and care in phlebotomy, EKG, and lab services for the patients of the Cancer Center Research Lab. The ideal candidate for this role should be able to perform in a high volume environment. KELLY ...

    9. Senior Biostatistician/RTP or Silver Springs, MD (Perm) - 1504779

        Seeking a Biostatistician to support commercial clinical research studies.  You will contribute to the development of the statistical aspects of clinical research studies, perform statistical analysis, interpret data, and prepare oral and written statistical reports of results. You will perform randomization and blinding of clinical trials and quality control for statistical analyses by ...

    10. Senior Manager of Clinical Operations RTP, NC or Boulder, CO - 1513913

        Responsibilities and Duties may include: ·         The Sr. Manager of Clinical Operations is assigned to lead and manage clinical trials and to oversee all operational aspects including budgets, timelines, resources, vendor selection and management as well as oversight of clinical team staff during study start-up, interim monitoring and closeout periods. Strong experience in Phase II-III ...

    11. Pharmacovigilance Safety Specialist

      A Drug Safety Associate (DSA), known also in the industry as a Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.   Morrisville or Raleigh, NC Safety Specialist Contract - BHCJP00013871 W-2 ONLY ...

    12. Programmer Analyst

      A Programmer Analyst job in Research Triangle Park, NC is now available for a six month plus contract courtesy of Adecco Engineering and Technology. In order to be considered for this job, candidates must possess a degree in computer or life science, along with at least two years of relevant work experience, or combined equivalent experience. Candidates must also posses a good knowledge of ...

    13. Associate Scientist

          Hello,   My name is Carlane and I represent The Fountain Group.  We are a national staffing firm and are currently seeking an Associate Scientist I position  for a prominent client of ours.  This position is located in Research Triangle Park NC. Details for he position are as follows:   Job Description:     Seeking a highly motivated scientist to work in the Chemistry Analytical ...

    14. Director/Senior Director Project Management (Clinical Research)

      The Director/Senior Director Project Management (DPM) mentors and leads project teams and facilitates an efficient and effective project management group by managing company processes and systems within the framework of the company’s mission statement, policy and philosophy. He/she provides strategic direction to the project management team and ensures staff development, training, performance ...

    15. Director, Pharmaceutical Development and CMC

        The Director, Pharmaceutical Development is responsible for leading CMC and pharmaceutical development activities for Liquidia’s internal and partner products, including activities required for the development and implementation of new drug delivery technologies and drug product formulations as well as their associated manufacturing processes and controls. The position will lead key CMC ...

    16. 97078 - Senior Clinical Project Manager - REMOTE

        Job Description: Summary of Key Responsibilities: The Senior Clinical Project Manager (Sr. CPM) is responsible for overall management, coordination, and supervision of multiple clinical research trial projects (including global projects) to ensure timely delivery of required objectives and timelines within the scope of clinical trial agreement and project budget.  Serves as the principal ...

    17. Regional CRA - US Telecommute

      The Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Company Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that ...

    18. Consultant Nurse

      Provides medical information with high quality customer service. Researches and responds to inquiries and documents appropriately according to Company and client guidelines. Identifies and records adverse events and product complaints. If needed, provides clinical trial information, after-hours on call support, as well as processes medical information requests via mail, fax, e-mail. BSN ...

    19. R&D Development Engineer

      Opportunity: Under minimal direction, responsible for the development and maintenance of respiratory or other medical products; organizes and manages multiple projects and insures projects are completed in a timely manner; creates design ideas for new products as well as creative solutions to existing products when problems arise or modifications are requested; and performs other related ...

    20. Data Management Project Manager-Clinical Research Organization

      Serve as lead data manager on assigned studies.  Responsible for administrative supervision of data management staff.  Provide management oversight of projects to assure quality and timely database deliveries.  Serve as primary liaison with clients and other departments.   ESSENTIAL DUTIES AND RESPONSIBILITIES:   Manage and work concurrently on multiple protocols. Create case report ...

    21. Vaccines Public Account Manager-Federal Market-NC/SC

      Requisition ID: WD35471 Vaccines Public Account Manager-Federal Market-NC/SC Develop, manage and grow key customer relationships by orchestrating the deployment of VBU resources to provide comprehensive immunization product and service solutions to strategically important accounts. Responsible for managing several projects at any given time . The implementation of an public sector vaccine ...

    22. Salesforce.com Administrator

      Opportunity: The Salesforce.com Administrator will play an important role in building and maintaining efficient and streamlined platform for managing and tracking customer relationships. This role will work closely with various customer groups to build upon our existing platform and help promote increased user adoption of the system through daily customer support. Division Information: The ...

    23. Director of Marketing, Latin America

      Opportunity: The Director of Marketing for Latin American leads all efforts relative to marketing strategies for Vascular, Anesthesia, Surgical, Respiratory, Interventional Access, Urology, LMA, Vidacare and Urology in region. In this regard, this position oversees through delivery of strategic and tactical plans that are achieved through direct sales and distributors. This role provides ...

    24. Senior Administrative Assistant

      Opportunity: The Senior Administrative Assistant to the Research & Development team for Anesthesia supports all administrative needs of not only the Vice President of the department, but also of the Senior R&D Manager, and associated needs of the 17-person US R&D engineering staff. This position also interacts with international R&D team members in Malaysia, but does not bear administrative ...

      1. Watson - Program Director, Health Cloud at IBM

        Crucial to the mission of IBM Watson Health, the Watson Health Cloud will bring together clinical, research and social data from a diverse range of health...

      2. Study Manager (Sr) - Program Oversight (Home based) / Pharma experience preferred at PPD

        Clinical monitoring of research studies, which includes production and approval. Develops/reviews budget for clinical....

      3. Program Manager (Vaccines & Infectious Disease) at ICON Clinical Research

        Are you a seasoned clinical research. Timelines, client specifications and Good Clinical Practices (GCPs). Full service project plans for clinical trials or a...

      4. PROGRAM DIRECTOR - Graduate Medical Education at Mount Sinai Health System

        Prepare, implement and monitor Health System GME budget, including oversight of Empire Clinical Research Investigator Program (ECRIP) grants....

      5. Clinical Team Manager at Theorem Clinical Research

        Theorem Clinical Research Inc. For more information about Theorem Clinical Research, please visit:. Clinical Team Manager (CTM)....