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Jobs (102 Matches)
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1. Clinical Research Associate   (Temporary)5 days ago
Real Staffing - United States, CA, San Jose - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionClinical Research Associate5-6 months with a possibility to extendStryker Endoscopy - San Jose, CARequired Participates in the design, administration and oversight of clinical and human factor/ergonomic studies. Studies may be conducted as either Investigator Initiated or Sponsor initiated studies.Review research projects for compliance with procedures, regulations, ...
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2. Clinical Project Manager   (Fulltime)5 days ago
Aerotek - United States, MD, Gaithersburg - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionThe Clinical Project Manager (CPM), serves as the primary contact to CROs, site investigators,study personnel, as well as internal departments to relay study progress, status and/orissues associated with the daily operations of one (or more) clinical studies. The CPM will beresponsible for all aspects of one ...
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3. In House CRA, Early Phase   (Fulltime)5 days ago
Joule' Clinical - United States, NJ, Morristown - Not rated - (view employer jobs)
Categories: Biotech, Pharmaceutical, ResearchJob DescriptionOur client is a growing pharmaceutical company and is currently hiring an In-House CRA / Project Coordinator. This is a PERMANENT position on-site 5 days per week in Morris County, NJ. Candidates with small pharma experience are preferred. Salary range: 70-85k based ...
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4. Clinical Site Manager - Global Fortune 150 Company   (Fulltime)236 days ago
Experis - United States, TX, Fort Worth - Not rated - (view employer jobs)
Categories: Biotech, Pharmaceutical, ScienceJob DescriptionThe Contract Senior Clinical Site Manager will be responsible for implementing and executing the client clinical trials in the sites assigned under his/her responsibility. He/she should ensure compliance with international guidelines, local regulations and corporate policies and procedures. Major Accountabilities (Describe the 5-7 ...
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5. Clinical Project Manager   (Fulltime)236 days ago
Real Staffing - United States, IL, Lake Forest - Not rated - (view employer jobs)
Categories: Biotech, Pharmaceutical, ResearchJob DescriptionThe Clinical Project Manager III will be responsible for overall project management of one or more clinical studies, including personnel development, mentoring of Clinical Research Associates / Sr. Clinical Research Associates and other clinical staff. The Clinical Project Manager III also serves as lead ...
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6. CRA or Sr CRA (In-house)   (Fulltime)236 days ago
Aerotek - United States, WA, Kirkland - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionPosition Overview:This position is responsible for:1. Serving as main point of contact between clinical site investigators 2. Serving as liaison between CRO 3. Providing oversight of clinical conduct to ensure that all trials are being conducted inaccordance with approved protocols, applicable regulations and GCP, work instructions,guidelines and/or policies.4. ...
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7. Clinical Trials Assistant or Sr.Clinical Trials Assistant   (Fulltime)236 days ago
Aerotek - United States, WA, Bothell - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionJOB SUMMARY:Assist clinical study teams in the execution of clinical trials with dotted line reporting to the study Protocol Lead (PL). Primary responsibilities may include establishing and maintaining the Clinical Trial Master File (CTMF) and Clinical Trial Management System (CTMS) in an inspection-ready state, and assisting with production ...
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8. Clinical Trial Assistant (CTA)   (Temporary)236 days ago
The Ascent Services Group - United States, CA, Redwood City - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionClinical Trials Assistant6-12 Month Contract Opportunity Redwood City, CADESCRIPTION The Clinical Trials Assistant (CTA) will support the clinical project team in the following areas: accurately update and maintain clinical systems and/or trackers within project timelines; prepare, handle, distribute, file, and archive clinical documentation and reports; review of study files ...
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9. Contract Clinical Research Associate   (Temporary)236 days ago
Global Employment Solutions Inc. - United States, IN, Indianapolis - Not rated - (view employer jobs)
Categories: Pharmaceutical, Biotech, NurseJob DescriptionSearch Term: Regional CRA, Contract CRA, Sr. CRA, Home-based CRA, Regional Clinical Research Associate, Regional CRA II, Sr. Clinical Research Associate, Senior Clinical Research Associate, Monitor, Contract CRA II, CRA III, Regional Monitor, Home-based Regional CRA, CRA, Contract Clinical Research Associate, Regional CRA Consultant, ...
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10. Contract Regional CRA   (Temporary)236 days ago
Global Employment Solutions Inc. - United States, IL, West Chicago - Not rated - (view employer jobs)
Categories: Biotech, Pharmaceutical, NurseJob DescriptionSearch Term: Regional CRA, Contract CRA, Sr. CRA, Home-based CRA, Regional Clinical Research Associate, Regional CRA II, Sr. Clinical Research Associate, Senior Clinical Research Associate, Monitor, Contract CRA II, CRA III, Regional Monitor, Home-based Regional CRA, CRA, Contract Clinical Research Associate, Regional CRA Consultant, ...
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11. Clinical Trial Associate   (Fulltime)251 days ago
Aerotek - United States, KS, Park - Not rated - (view employer jobs)
Categories: Other, Research, ScienceJob DescriptionClinical Trials Assistant:Summary: May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.PrimaryDuties: The Clinical Trials Assistant (CTA) will support the clinical project team in the following areas: accurately update and maintain clinical systems within project ...
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12. SSRS Clinical Research Developer   (Fulltime)251 days ago
ERP Recruiting - United States, OK, Cleveland - Not rated - (view employer jobs)
Categories: Information TechnologyJob DescriptionSSRS Clinical Research Developer Direct Hire Cleveland, Ohio THE ROLE YOU WILL PLAY FOR THE SSRS CLINICAL RESEARCH DEVELOPER: * The Report Developer works with customers and peers to design, develop, modify and test data marts and data models that meet the customer's needs. * Requires a thorough understanding ...
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13. Clinical Research Coordinator   (Fulltime)251 days ago
Aerotek - United States, MA, Boston - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionMUST HAVES:-Collecting Informed Consent Forms and Consenting patients-Work with study start up documents and 1572s.-Direct Patient InteractionThis candidate will be consenting patients, scheduling their appointments and collecting all the needed clinical documentation including ICF, 1572 and regulatory documents. They will be interacting with patients, PIs, Nurses and CRA's ...
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14. Clinical Research Associate   (Fulltime)251 days ago
Aerotek - United States, MD, Rockville - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionPermanent CRATo monitor clinical study sites to ensure compliance with the clinical trial protocol, to verify clinical site activities, to conduct on-site visits, to review Case Report Forms (CRFs) and to manage clinical research sites.Minimum qualifications:1 year of onsite monitoring experience as a CRA2 years of clinical experience50% ...
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15. Expert Clinical Manager III   (Temporary)251 days ago
Advanced Clinical - United States, NJ, East Hanover - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 431520Expert Clinical Manager IIIOVERVIEWResponsible for all operational aspects of 1 or more OGD clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned.Ensure all operational trial deliverables are met according ...
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16. Publication Project Coordinator / Biotech - Pharma   (Temporary)251 days ago
Kforce Technology - United States, CA, Thousand Oaks - Not rated - (view employer jobs)
Categories: Information TechnologyJob DescriptionRESPONSIBILITIES:Kforce has a client seeking a Publication Project Coordinator: Global Health Economics (GHE) in Thousand Oaks, CA. This position will be responsible for coordinating global publication projects, and providing support for publication process and system operations for the GHE Oncology Therapeutic area.For all scientific, medical and technical ...
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17. Clinical Trial Coordinator   (Temporary)251 days ago
Advanced Clinical - United States, NJ, Woodcliff Lake - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 431605Clinical Trial CoordinatorOVERVIEWClinical Trial Coordinator Basic understanding of clinical study processes, with specialized technical skills to deliver own work within the clinical study team.Ability to work semi-autonomously with strong organizational, prioritization and analytical skills.Liaises with other functional areas on study-related processes.Effectively manages time to meet project ...
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18. Sr. CRA - Regional   (Temporary)251 days ago
Advanced Clinical - United States, MA, Cambridge - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 431615Sr. CRA - RegionalOverview:Phase Oncology studiesFocus in early stage oncology studies Ph 1-2Well versed in InForm, Rave, and other types of EDC's.Job Requirements
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19. Reseach Assistant in Applied Behavior Analysis, P&A Lindens Program   (Fulltime)251 days ago
Bancroft - United States, NJ, Haddonfield - Not rated - (view employer jobs)
Categories: Entry Level, Nonprofit - Social Services, ResearchJob DescriptionThe following statements are intended to describe the general nature and level of work to be performed. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of an incumbent. Position Summary: Serves ...
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20. Director Clinical Operations   (Fulltime)251 days ago
Aerotek - United States, CA, San Diego - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionThis position is responsible for the oversight of the oncology program, including protocol development, study related materials, clinical study budget, contract, and timelines. He/she is responsible for the execution of projects and manages cross functional activities in order to ensure the departmental and corporate goals and objectives are ...
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