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Director of Research (Oncology)
PhD and/or Nurse Practitioner
Monday - Friday
Salary Position. Benefits, pension, malpractice
Responsibilites include, Research Compliance, Study Procurment, Research Expansion
... the necessary physician signatures and clinical staff signatures for clinical documentation. *Responsible for accurately maintaining ... documentation. *Responsible for accurately maintaining clinical Medical records. Ensures clinical documentation is copied..
Burn and Wound Clinic Manager (Outpatient)','1642534','','','!*!Manages the program and staff of the wound care services department. Develops and implements wound care services in accordance with the policies of the hospital and ..
... problem-solving/solution oriented skills to develop and evaluate asset level strategies from lead to legacy.Develops and maintains up to date clinical plan timelines (using ProChain/CCPM methodology, or MS Project) and process maps (as appropriate).Monitors and reports performance to plan and fast ...
... , and 4) resolution of complex issues and requests escalated from the division Service Desk or other division or facility service resources. The Division Clinical Specialist coordinates division-wide parameter management, develops education/training materials for new applications, manages validation ...
... (SDV) progress, query aging, monitoring resource requirements, etc) to ensure performance maximizes efficiency, quality, ICH/GCP adherence, and meet clinical trial and corporate goals.
Provide support to field CRAs and may assist in the initiating, monitoring and coordinating day-to-day operations ...
first-professional programs. More than 4,000 students learn alongside faculty
members who also make meaningful medical discoveries and provide expert
clinical care through 1.5 million patient-visits annually. A hub for research
and innovation, CU Anschutz receives over $400 million in research ...
**Job** _Clinical Research (M.D.)_
**Other Locations:** _NA-US-NJ-Rahway_
**_Title:_** _Director, Clinical Research - Oncology_
**_Primary Location:_** _NA-US-PA-Upper Gwynedd_
**_Requisition ID:_** _CLI005021_
... utilizes multiple vendor-packaged and UW Medicine EHR applications across multiple care settings and healthcare teams. The Clinical Informatics Analyst will demonstrate primary expertise in one EHR but must also maintain working knowledge of the other EHR to leverage appropriate transitions of care ...
... , clinical protocols, consent forms, Study Operations Plan, Monitoring Plan, Communication Plan, investigator brochure, clinical study reports, INDs/CTAs, marketing applications, annual regulatory reports, etc.
Coordinate the RFP process, review vendor proposals, and negotiate budgets for assigned ...
... Understanding of reporting tools functionality and capabilities
Must be able to drive to assigned sites to complete work
Proficiency in various programming and clinical application reporting tools
Customer service orientation and/or training
Bachelor's degree preferred
... and Key Opinion Leaders.
Education: MD / PharmD / PhD in pharmacology or related area required. MD (Clinical Pharmacology Board Certified) preferred.
* Minimum of 10 years experience required, including at least 5 years relevant pharmaceutical or related ...
... , training guides), as applicable.
BA/BS or equivalent or any relevant and qualifying training with a minimum of 4 years of relevant clinical trial management experience.
Requires effective organizational and communication skills.
Knowledge of CFR and GCP/ICH requirements is required ...
... project and ensures DMP is followed according to study design and requirements.
Develop Case Report Form (CRF), electronic and/or paper
Develop database (DB) clinical trial data specifications, including eCRF design, user requirements, edit rules/checks, query logic and data validations
Lead EDC ...
... trial program. Communicates project status and issues to management and other team members and ensures that project team goals are met.
Reviews and approves all clinical study conduct documents including study concept document, relevant manuals, protocol, IB, ICF, CRF (and eCRF), site monitoring ...
27. Plan and participate in audits and monitoring visits, and the development of protocol re-lated reports.
28. Creatively solve clinical trial problems of logistics, manpower, and study execution; rec-ommend approaches and solutions to problems such as protocol compliance ...
... (e.g. pre-IND/ end Phase III/ Scientific Advice/ pre-submission/ mid- and late cycle review) where required.
* In collaboration with Clinical Operations and Commercial Development, identify key investigators. Develop and maintain excellent relationships with key investigators and scientific leaders ...
... actions, following Indivior’s medical governance policies.
Contributes to authorship or major contribution, review and approval of key documents such as Clinical Investigator Brochure (CIB), INDs, CTX/ CTAs, NDAs and publications in biomedical/scientific journals in collaboration with project team ...