- US Tech Solutions (North Chicago, IL)
- …Communication Skills; providing updates across functions; written and verbally 3 . **Contractual or Paralegal** experience highly preferred **Purpose:** The Contract ... including **Clinical Study Agreements, Confidential Disclosure Agreements, Master Agreements, Investigator Initiated Agreements, Service Agreements** ect In partnership with… more
- Beth Israel Lahey Health (Boston, MA)
- …patients' medical record. Verifies information with clinical research nurse and/or principal investigator . 3 . Learns about informed consent and assist in ... and fellows. Learns to identify any problems with protocol compliance and notifies principal investigator and/or research...in an academic program (high school through graduate school) 3 . 0-1 years related work experience required. 4. Basic… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** **Principal Investigator , Dr. Mustafa Khokha, MD, is looking for a Research Associate III to join the team!** The Khokha Lab uses Xenopus, a frog ... and/or clinical activities, including but not limited to, budgetary/financial compliance , preparation of grant proposals, and creating independent presentations. Not… more
- Bozeman Health (Bozeman, MT)
- …(NCI), and other regulatory agencies. Responsibilities include ensuring protocol compliance , recruiting and caring for study participants, documenting study ... Bozeman Health policy, and other registry requirements. + Ensure compliance with research protocols, regulatory requirements, and institutional policies while… more
- University of Miami (Miami, FL)
- …data collection/recording, and daily operations of moderate risk clinicalresearch protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... practice standards and clinical credentials as delegated by thePrincipal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse… more
- AbbVie (Mettawa, IL)
- …Tik Tok (https://www.tiktok.com/@abbvie) . Job Description *Must be willing to come onsite 3 days per week in Mettawa, IL. The Medical Director, Medical Affairs ... analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses.… more
- Community Health Network (Indianapolis, IN)
- …independently running and operating multiple research protocols in conjunction with the Principal Investigator and serves as a lead in the clinical research unit. * ... conducting qualification, study initiation, interim monitoring, and close-out visits at investigator sites in conjunction with the Clinical Research Manager. **Your… more
- University of Miami (Miami, FL)
- …collection/recording, and daily operations of moderate risk clinical research protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... standards and clinical credentials as delegated by the Principal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse events… more
- US Tech Solutions (North Chicago, IL)
- …**Clinical Study Agreements, Confidential Disclosure Agreements, Master Agreements, Investigator Initiated Agreements, Service Agreements** ect In partnership with ... Communication Skills; providing updates across functions; written and verbally 3 . **Contractual or Paralegal** experience highly preferred **Responsibilities:** *… more
- New York University (New York, NY)
- …to earlier detection of local recurrence than the traditional clinical pathway, and ( 3 ) to further optimize the POCOCT for precision lesion diagnostics of MT and ... well to various members of the study team including the Principal Investigator ; Listen carefully to others to respond appropriately, answer questions or obtain… more