- Astrix Technology (Boston, MA)
- …nursing. + 10-12 years of professional experience , including at least 3 years as a Clinical Trial Manager (CTM) or Clinical Trial Project Manager . + ... **Senior Clinical Project Manager ** Clinical ...Proficiency in ICH GCP guidelines, US regulations, project management, clinical operations, study budgets, and timeline management.… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …locations. This role is not eligible to be fully remote is not available._ The ** Manager Clinical Study Lead** (CSL **)** may perform the following ... studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug... in global clinical trial operations including experience developing protocols and key study documents… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …internal and external studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation ... office locations. Fully remote is not eligible._ The **Senior Clinical Study Lead** (CSL) is expected to...implements the operational strategic direction and guidance for respective clinical studies + Demonstrates expert knowledge and… more
- BeOne Medicines (Emeryville, CA)
- …+ Monitors resource utilization over the study life cycle + Ensures clinical studies at a project level are executed within endorsed time, quality, ... timelines and budget + Leads all aspects of assigned clinical study (ies) + Leads global cross-functional ...studies + 7 or more years of progressive experience in clinical research within biotech, pharma… more
- BeOne Medicines (San Mateo, CA)
- …regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional study ... Study Report in collaboration with Global Clinical Study Manager and Medical...**Other Qualifications:** + 6 or more years of progressive experience in clinical research within biotech, pharma… more
- Beth Israel Lahey Health (Boston, MA)
- …advisors, study sponsor, subcommittee members and other collaborators. Previous experience in clinical research and interest in Ob-Gyn research highly ... research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research… more
- Arkansas Children's (Little Rock, AR)
- …of the study start-up process, ensuring the timely activation of clinical studies while maintaining compliance with institutional, state, and federal ... Type:** Full time **Department:** CC033020 Clinical Research Operations **Summary:** The Study Start-Up Project Manager serves as the institutional lead and… more
- AbbVie (Mettawa, IL)
- …+ Experienced user of clinical trial systems (eg, EDC, CTMS, eTMF) + Experience with study initiation through study completion is preferred. Additional ... protocol and associated documents (eg, informed consent forms, case report forms, Clinical Study Report, publications). + Leader of the cross functional … more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The ** Clinical Study Build Programmer - eCOA** is responsible for programming and testing ... flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with...collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Clinical Study Build Programmer is responsible for programming and testing clinical ... collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager...(or bachelor's degree plus 3 or more years of experience in clinical data management, database programming… more