- Parexel (Baltimore, MD)
- …is complete** **(including but not limited):** + Execute all appropriate Sub- Investigator responsibilities on assigned projects. + Provide Information and obtain ... + Executes and coordinates a variety of specialized clinical research activities ensuring compliance with GCP + Assists with the medical and clinical oversight of… more
- University of Pennsylvania (Philadelphia, PA)
- …Coordinator to organize, coordinate and implement different phases of investigator -initiated and industry-sponsored clinical trials of novel therapies or currently ... testing; within the EMR or other tools + Attend Investigator Initiation meetings + Obtain slides from pathology and...and/or CROs. + Show vigilance in patient safety, protocol compliance , and data quality. + Adhere to all University… more
- US Tech Solutions (North Chicago, IL)
- …including Clinical Study Agreements, Confidential DisclosureAgreements, Master Agreements, Investigator Initiated Agreements, Service Agreements etc. In partnership ... as needed forClinical Study Agreements, Confidential Disclosure Agreements, MasterAgreements, Investigator Initiated Agreements, Service Agreements, and anyother procurement agreements.… more
- Office of the Inspector General for Tax Administration (Washington, DC)
- …operations of Internal Revenue Service (IRS) and Related Entities. As a criminal investigator , you will be called upon to spearhead the largest, most complex, and ... Privacy Rights - FBI, FD-258 Privacy Act Statement - FBI, and SEAD- 3 -Reporting-U.pdf (dni.gov). Qualifications You must meet the following requirements by the… more
- IQVIA (Durham, NC)
- …translating into appropriate budgets/contract exhibits for company sponsored and investigator initiated clinical trial agreements and other ancillary contract ... documents as they relate to various clinical projects.Analyze investigator grants for fair market value aligned with regional knowledge and the J&J pricing… more
- McLaren Health Care (Bay City, MI)
- …studies; assisting in the informed consent process; monitoring research study compliance ; collecting and submitting data; coordinating required study procedures to ... the other staff in determining eligibility of potential patients. 2. Assists the investigator with the informed consent process and assures that the research team… more
- Houston Methodist (Houston, TX)
- …abstracts, manuscripts, review articles, grant applications, clinical study protocols, investigator brochures, consent forms, presentations and progress reports for ... data considering scientific communications best practices. + Works with Principal Investigator (s) to develop, present, and bring to final submission high quality,… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …actions (eg, amendments, continuing reviews, safety reports, deviations, etc.) for compliance with relevant regulatory requirements and draft a Protocol Evaluation ... detachments. + Evaluating research protocols and protocol lifecycle actions for compliance with relevant regulatory requirements and drafting a protocol evaluation… more
- CUNY (New York, NY)
- …of administrative functions in consultation with the Principal Investigator /Faculty Advisor, while providing basic program information, registration instructions, ... registration and orientation spaces. + In collaboration with the Principal Investigator (PI)/Faculty Advisor, create and maintain the program's fiscal plans +… more
- University of Utah (Salt Lake City, UT)
- …Biology, or a related field from an accredited US institution with up to 3 years of post-graduation research experience. Candidate must have a track record in ... * **Grant Success** : Pursue independent grant funding as a Principal Investigator or co- investigator . * **Ethical Understanding** : Strong understanding of… more