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The successful candidate will have a strong foundation in project management, outsourcing, and/or vendor management in this critical role along with experience in Clinical Trial Delivery or Drug Development Lifecycle.
$70 - $80 an hourExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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You will act as a liaison between cross-functional groups to effectively execute clinical trials. They are looking to bring on an experienced Associate Director of Clinical Program Management to support the development of their mid-stage clinical pipeline.
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Works collegially with PSR Supervisor and Clinical Supervisors in other departments. Participates in interviewing and hiring new clinical personnel and responsible for clinical orientation in conjunction with Practice Manager.
$69.68 - $92.33 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Valid unrestricted state-issued license to practice clinical or counseling psychology. A doctoral degree (Ph. D. or Psy. D.) in clinical psychology or counseling psychology. Completion of a clinical internship.
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Clinical Trials Manager, Clinical Operations - Oncology (CTM) CLINICAL OPERATIONS: Clinical Operations is responsible for the execution of all Phase 1-4 clinical trials, across all therapeutic areas, around the world.
$143,225 - $185,350 a yearExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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The Director of Clinical Data Management (CDM) will play a pivotal role, responsible for overseeing all aspects of CDM. Reporting to the Head of Biometrics, you'll drive strategic planning, ensuring data integrity and compliance, and collaborate with key stakeholders across the company to drive the success of our clinical trials.
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Delivers pharmaceutical care through the provision of patient-centered clinical service, medication information, education, medication preparation and distribution that ensures safe, effective, and cost efficient medication therapy.
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Most trials don't require much effort and will be located near you. Potentially get paid to access the most cutting edge medicines combating your disease. Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
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Oversees performance and deliverables of data management service providers on assigned studies and programs as well as manages all aspects of the clinical trial data management process from study start up to post database lock for Electronic Data Capture (EDC) and paper CRF trials.
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Option 1 Staffing is an award-winning, statewide, recognized leader in staffing and recruiting, specializing in placing the highest caliber of Non-Clinical Healthcare, Information Technology, Supply Chain, Administrative/Office, and Accounting/Finance professionals in contract and direct-hire opportunities.
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Licensed Clinical Drug and Alcohol Counselor (LCADC) is preferred. Preferred: Licensed Clinical Social Worker (LCSW), Licensed Psychologist (LP), Licensed ProfessionalCounselor (LPC), or Registered Nurse is required.
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Providing clinical and administrative supervision to admissions coordinator. In addition, provide consultation to program leaders on administrative matters as indicated and aid in the planning, implementation, and dissemination of clinical research.
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Masters degree in a clinical field of nursing or a clinical field related to nursing including but not limited to psychology, public health, social work, education, health sciences, behavioral sciences, nutrition, and bioethics from a nationally accredited masters/post masters nursing academic program.
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You will join the Clinical IT product team, where you will work closely together with the Product Owner, Product Coach and other team members. + With the rest of your team, you will perform daily monitoring of application in production, mange Service now ticketing queue for timely resolution and work with cross functional teams to help Clinical stake holders.
$135,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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S global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department. The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of.
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Title: clinical trials Company: Hennepin Healthcare Research Institute in Foster City, CA
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