- Gilead Sciences, Inc. (Foster City, CA)
- …are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical ... clinical development component(s) in the preparation/review of regulatory documents, investigator brochures and development plans. + Coordinates the collection and… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …+ Assisting in the coordination and planning of meetings (eg Investigator Meetings, Kick-off meetings). + Conducting monitor training. + Performing ... visits, in conformance to all relevant laws, regulations, guidelines and internal SOPs/policies. + Understanding and implementing processes for distribution and… more
- University of Pennsylvania (Philadelphia, PA)
- …wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. Research ... of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying...may take a lead role in study communication with internal and external groups. Work directly with investigators to… more
- Beth Israel Lahey Health (Boston, MA)
- …degree program. In collaboration and under the mentorship of the Principal Investigator , a Pre-Doctoral Research Fellow engages in activities that will further his ... 1. Conducts research under the guidance of the Principal Investigator or designee as part of a degree program.... or designee as part of a degree program. 2 . Researches and collects study data through monitoring devices… more
- University of Pennsylvania (Philadelphia, PA)
- …and translational research studies led by the Susztaklab, including multi-site investigator -initiated projects such as Trident, PGDD, and KRAD. The role involves ... subject recruitment, data collection, regulatory documentation, and communication with internal and external collaborators. The individual will work closely with… more
- Wayne State University (Detroit, MI)
- …Essential functions (job duties): Under the direction of the Principal Investigator , provide scientific and technical assistance to complete laboratory based, ... the needs of the research protocol. With the assistance of the Principal Investigator , find and write research grants with the goal of obtaining additional research… more
- Beth Israel Lahey Health (Boston, MA)
- …contracts with physicians and nurses and knowledge of the protocol. (essential) 2 . Checks all eligibility and ineligibility criteria with the patients' medical ... record. Verifies information with clinical research nurse and/or principal investigator . (essential) 3. Discusses informed consent with patients. Interacts with… more
- University of Pennsylvania (Philadelphia, PA)
- …Affairs Start-Up Specialist is expected to oversee the development of investigator -initiated research protocols, the development and submission of FDA IND ... as, to provide direct regulatory/compliance guidance and oversight of investigator -initiated trials and investigator -initiated multi-site trials. Qualifications:… more
- Arkansas Children's (Little Rock, AR)
- …projects, supervised by the Clinical Research Supervisor and Principal Investigator . Responsibilities include meticulous adherence to study protocols, managing data ... a related field of study. **Required Work Experience:** High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED. **Recommended Work Experience:**… more
- University of Pennsylvania (Philadelphia, PA)
- …manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator , manager, and study team to address study needs, implement approved ... changes, and monitor outcomes. Contributes to investigator -initiated, multi-center, and patient-oriented clinical and translational research studies. Job Description… more