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clinical research in Newark

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  1. Sr. Mobile Application Engineer at Medidata Solutions

    We are publicly traded (MDSO) with over 700 customers, customer retention rates above 99%, and the experience of supporting more than 10,000 clinical trials....

  2. Director, Engineering (Mobile) at Medidata Solutions

    We are publicly traded (MDSO) and the market leader for clinical trial software with over 700 customers. We continue to maintain a 99% customer retention rate...

  3. Project Statistician at Ferring Pharmaceuticals

    Driven by research and a passion for science. • Contribute to clinical development programs & study designs....

  4. Director, Pharmacovigilance & Drug Safety (MD) at PTC THERAPEUTICS

    Responsible for the oversight of Clinical Research Organizations (CROs) activities for both post marketing and clinical trials....

  5. Dir, Regulatory Affairs at PTC THERAPEUTICS

    Marketing and clinical trial applications and their maintenance, amendments, and variations, and other relevant regulatory filings;...

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    1. Sr. Clinical Research Scientist

      Write clinical study-related documents (e.g., protocols, clinical study reports, investigator’s brochures) Present comprehensive and/ or detailed summary of study resultsContribute to protocol development and data interpretationOffer scientific input to the operational strategy and feasibility of clinical studiesAct as a scientific expert on studies in therapeutic areaReview scientific ...

    1. Registered Behavior Technicians (RBT)/ABA Therapist at Innovative Therapy Group

      Clinical Mentoring Program. Provide teachers with research based interventions for skill acquisition goals. Innovative Therapy Group seeks a Full-Time Special...

    1. Clinical Scientist

      Lead background research on studies to form references/scientific baseApply knowledge of clinical trial design to advance specific study ideasContribute in discussions regarding routine features of study designMature clinical documents in agreement with FDA regulationsDeliver input to the design of CRFsIdentify and resolve issues related to study design and implementationHelp with the ...

    1. Board Certified Behavior Analyst (BCBA) at Innovative Therapy Group

      Clinical Mentoring Program. Provide teachers with research based interventions for skill acquisition goals....

    1. Drug Safety Physician

      Vivos Professional Services is currently seeking candidates for a Pharmacovigilance Physician opportunity in Parsippany, New Jersey. Incumbent performs medical assessment and related activities for single cases, including collecting additional follow-up information as necessary, medical evaluation of quality defects, review of the line listings of single cases and preparation of investigator ...

    1. Special Education Teacher/BCBA at Innovative Therapy Group

      Clinical Mentoring Program. Provide teachers with research based interventions for skill acquisition goals. Innovative Therapy Group seeks a Full-Time Special...

    1. Entry Level Laboratory Informatics Associate

      LabAnswer is hiring for our entry-level Laboratory Informatics Associate Training Program in Orlando, Florida. The training program is the springboard to a career as a Consultant at LabAnswer.Laboratory Informatics Associates who complete our in-house training program will be taught how to be a Consultant qualified to lead and manage key portions of projects, using specialized and expert ...

    1. Senior Human Subject Protections Analyst at Rutgers University

      New Jersey’s academic health center, Rutgers Biomedical and Health Sciences ( RBHS ) takes an integrated approach to educating students, providing clinical care...

    1. Sr. Manager, Clinical Research

      Senior Manager, Clinical Research – Princeton, NJ areaESSENTIAL DUTIES AND RESPONSIBILITIES: include the following:Writing and finalizing protocols for the conduct of interventional clinical trials and non-interventional trials as well as studies designed for the retrospective collection of data.Selecting and qualifying sites for the performance of clinical trials.Reviewing informed consent ...

    1. Senior Consultant, Data Management at LabAnswer

      Opportunities to work across a variety of laboratory environments (analytical testing, biotech, clinical trials, forensics, medical device, pharmaceutical,...

    1. Clinical Project Manager (CPM) Oncology Trials

      Clinical Project Manager (CPM) Oncology TrialsThe ​Clinical Project Manager (CPM) responsible for:Managing early phase clinical trials as well as managing & scheduling the CRAs assigned to the project.Preparing the project/monitoring plan for the studies.Monitoring budgets and fund expenditures for the assigned trialsPreparing the Study Budgets.Performing Site Qualification VisitsImplementing ...

    1. SCIENTIFIC AND LABORATORY INFORMATICS MANAGEMENT CONSULTANT at LabAnswer

      Opportunities to work across a variety of laboratory environments (analytical testing, biotech, clinical trials, forensics, medical device, pharmaceutical,...

    1. Pharmacovigilance/Drug Saftey Leader

      Hello, We are looking for an experienced and qualified candidate for a Drug Safety Lead Role for a Global Pharma Client.Education:MD REQUIRED (Foreign MD will also be considered)Duties:Performs medical assessment and related activities for single cases, including collecting additional follow-up information as necessary, medical evaluation of quality defects, review of the line listings of ...

    1. Medical Science Liaison at Otsuka Pharmaceutical

      Advanced degree in Pharmacy, Medicine, Biological Sciences, Health Services Research or Public Health, (Pharm.D., M.D., Ph.D....

    1. Clinical Nurse Leader Nursing Administration FT Day

      Description: The RN CNL is an advance generalist who directs and can provide comprehensive preventative and wellness care, as well as the spectrum of acute, episodic, chronic and end-of-life to our patients. The CNL serves as a leader, mentor and consultant to the healthcare staff; s/he demonstrates both analytical and creative approaches to management of complex patient care and serves as a ...

    1. Senior Medical Science Liaison, Oncology (NE/IO/MO/KS/KY) at Astellas Pharmaceuticals

      Identifying, qualifying and recommending appropriate KEEs for participation in Astellas clinical studies. 3+ years of industry Scientific Liaison experience or...

    1. Clinical Project Manager

      Well established international contract research organization serving both commercial as well as government markets, is conducting a search for a full time Clinical Project Manager to be based at the company's headquarters in Princeton NJ.Responsibilities:Oversees assigned studies and accountable for results for all components of studyReviews and provides input to new project proposals ...

    1. Inpatient/Outpatient Certified Coding Specialist III at Mount Sinai Health System

      Purposes, data retrieval, education, to support medical research activity,. Through unrivaled education, research, and outreach in the many diverse....

    1. Emergency Room Nurse (ER RN) (8667)

      About the Opportunity A respected healthcare facility located in Jersey City is actively seeking a compassionate and empathetic Registered Nurse (RN) for a promising opportunity within their Emergency Room (ER). In this role, the ER Nurse will assist in the development, implementation, and evaluation of standards of care and professional practice in collaboration with members of the ...

    1. Senior Medical Science Liaison- Oncology (South Central) at Valeant

      Policy on Clinical Trials. Strong relationship-building skills, particularly with the research community. Thus, the MSL has significant responsibility and is...

    1. CLINCIAL RESOURCES DIRECTOR, CLINICAL FIELD RESOURCES

      CLINCIAL RESOURCES DIRECTOR, CLINICAL FIELD RESOURCES - PRINCETON, NJScientific Search client has an immediate need for a Clinical Resources Director. This is a full time direct hire opportunity with a dynamic organization. This position is located in Princeton, NJ & reports to the group President. ·         Directs and oversees the activities of the clinical field support group. Manages the ...

    2. Project Specialist - Scientific - III

      Qualifications:Education: • Bachelor's degree required in Science, Finance/Accounting, Business, IT or Engineering field. • Five years relevant experiences in Pharma industry required Required: • Demonstrated ability to apply strategic thinking to project requirements • Ability to demonstrate strong business acumen in daily decisions • Excellent analytical skills with strong portfolio and ...

    3. Scientific Project Specialist (Project Management)

      *Please note that this is a 2 year contract assignment. Candidates cannot start an assignment until background check and drug test is completed*Responsibilities: The candidate will support CORE scientists to manage project information in the book of business (BoB) database.  In addition, the new hire will be responsible for ensuring work is following current  CORE processes and policies. ...

    4. Clinical Manager (440180)

      OVERVIEW:Provides leadership and day-to-day guidance to internal and External Service Provider (ESP) study team for all protocols within an assigned program. Ensures cross-study consistency in protocol design, data analysis and reporting. Interacts with expert physicians, investigators, ESP personnel, and functional area staff to ensure program strategy and objectives are understood and ...

    5. Financial Coordinator - Temporary Opportunity

      GENERAL PURPOSE OF THE JOB: The individual in this position will manage a case load of dialysis patients to help the patient understand and utilize their financial options to pay for their healthcare services. Research, identify, and coordinate the varied insurance options with the clinic's patients who are undergoing treatment, in effort to maximize company revenue. The Financial ...

    6. Clinical Scientist

      The Clinical Scientist serves a medical research function and applies a broad knowledge of clinical research activity, therapeutic area knowledge and regulatory requirements to facilitate the development and implementation of clinical studies. The primary objective and purpose of this position is ensuring that clinical trial protocols and study reports are developed and written with ...

    7. Aggregate Reports Manager, Drug Safety

       Job Title : Aggregate Reports Manager, Drug SafetyDuration : 2 + year contract on W2Location : Rahway NJ or Upper Gwynedd PA.Qualifications:This position in Global Safety requires a Bachelor's degree, preferably in nursing, pharmacy or a biological science. At least three years of experience in a hospital, pharmaceutical, or research position. Prior experience in coordinating and overseeing ...

    8. Director - Biostatistical Services

      Our client, a well established international contract research organization serving both commercial as well as government markets, is conducting a search for a Director of Biostatistical Services. . This 'hands-on' leadership position oversees statistical programming team and has the following responsibilities: Ensure successful completion of programming (tables, listings and graphs) for ...

    9. Sr. Manager, Clinical Research

      Senior Manager, Clinical Research – Princeton, NJ areaESSENTIAL DUTIES AND RESPONSIBILITIES: include the following:Writing and finalizing protocols for the conduct of interventional clinical trials and non-interventional trials as well as studies designed for the retrospective collection of data.Selecting and qualifying sites for the performance of clinical trials.Reviewing informed consent ...

    10. Data Management Associate (439895)

       OVERVIEW:ESSENTIAL DUTIES & RESPONSIBILITIES:•Assist the Data Management Department with all data management activities from study start-up to database lock.•Assist with review of Case Report Forms, Edit Checks, Data Management Listings, Query Listings, and Patient Profiles for data cleaning.•Assist with oversight of vendor activities to ensure quality and timely deliverables.•Coordinate ...

      1. Principal Medical Writer at Sanofi

        Good understanding of drug development, clinical research, study design, biostatistics, pharmacokinetics, the regulatory environment, and medical terminology....

      2. Senior UI Engineer at Medidata Solutions

        We are publicly traded (MDSO) with over 700 customers, customer retention rates above 99%, and the experience of supporting more than 10,000 clinical trials....

      3. LabWare Validation/Training at LabAnswer

        Opportunities to work across a variety of laboratory environments (analytical testing, biotech, clinical trials, forensics, medical device, pharmaceutical,...

      4. CTA Associate Line Manager position at Quintiles Transnational

        Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies that are appropriate to their experience and...

      5. Director, Quality & Training Development at PRA Health Sciences

        Clinical Trial Process Improvement :. Oversees Story Boards for Clinical Development Programs and pivotal clinical trials to implement a risk based mitigation...