- Houston Methodist (Houston, TX)
- …IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory compliance. Meets with study monitors. Maintains ... of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than 1,387 … more
- Sumitomo Pharma (Austin, TX)
- …International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Houston Methodist (Houston, TX)
- …cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than ... and safety of research participants, gathering patient data for clinical research activities via methods specified in the study...be sent to the Sponsor. + Identifies and recruits clinical research subjects and monitors enrollment goals. + May… more
- Houston Methodist (Houston, TX)
- …cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than ... for coordinating processes and a system for matching the research and clinical interest of faculty and/or physicians within Houston Methodist Research Institute… more
- Houston Methodist (Houston, TX)
- …cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than ... FTEs extramural funding of less than $2 million and lab or clinical -based research. **SERVICE ESSENTIAL FUNCTIONS** + Plans and organizes day-to-day department… more
- Astellas Pharma (Dallas, TX)
- … trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical ... will manage the site/sponsor relationship as it relates to clinical trial delivery through consistent communication and...Trials may include both early and late phase clinical trials . + Develops meaningful site relationships… more
- Edwards Lifesciences (Austin, TX)
- …**As the Manager of Clinical Project Management** , you will manage clinical trials activities and ensure all applicable regulatory requirements are met. ... role requires the ability to synthesize large sets of clinical trial data to support innovative operational...trial startup and early-phase execution for domestic US trials + Experience with RAVE databases (eg report/listing generation,… more
- Parexel (Austin, TX)
- …fulfill aspirations of the client Medicine Excellence to take up medical responsibilities of clinical trials within Clinical Development & Operations by a ... at the trial level throughout the preparation, conduct and reporting phase of clinical trial . During the clinical trial , SP is responsible to provide… more
- Otsuka America Pharmaceutical Inc. (Austin, TX)
- …major impact on human health. OPDC develops promising drug candidates, starting with clinical trial management, and then planning the strategy for drug approval, ... clinical stages to post commercialization, with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is… more
- Parexel (Austin, TX)
- …is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study ... and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg enrollment, database release), to safeguard the… more