Manager II: Late Phase Oncology; ISR/CO Study Manager (Sponsor Dedicated/ US Remote) Syneos Health® is a leading fully... and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether...
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description REMOTE: We welcome applicants... from all locations within the US. Must be legally authorized to work in the United States without sponsorship. Must be able to pass...
an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate... about. Job Summary We are seeking a Study Coordinator for our Safety Assessment site located in Reno, NV. The following...
our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act... and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy...
, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays... at a CRO in Study Start-Up Project management experience and demonstrated role in developing others Strong oral and written...
, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays... artery diseases. 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up...
, Study Training Compliance and DOA Matrix Management, to join our dynamic Central Support Operations team, part of the Global... Expansion and Study Operations department. The Specialist, Study Training Compliance and DOA Matrix Management within Central...
Clinical Study Specialist IV Neenah, WI 12+ Month Contract Rate: $40.00/hr W 2 Hours will vary based on business... needs and are NOT guaranteed (some weeks they could work 20-30 hours, some weeks they could work zero hours). Candidates...
, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays... at a CRO in Study Start-Up Project management experience and demonstrated role in developing others Strong oral and written...
-based Regulatory Submissions Coordinator to join our Study Start-up team. This position works both independently... and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process...
by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing... in drug development (including experience with IND and NDA submissions). Able to manage study start-up, and directs...
Study Start Up Associate II - Medical Device - Arden Hills, MN ICON plc is a world-leading healthcare intelligence.... Your responsibilities will include: Work independently and proactively to coordinate all necessary activities for site regulatory...
Employment as a Contingent Worker aligns well with individuals seeking career flexibility and non-traditional work... for engaging work. As a Contingent Worker, you will not be employed Daiichi Sankyo, Inc. You will be employed by our Managed...
Global Study Manager (hematology/oncology) ICON plc is a world-leading healthcare intelligence and clinical research..., and we welcome you to join us on our mission to shape the future of clinical development What you will be doing: Contribute to the development of study...
, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays... artery diseases. 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up...
The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the... global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out...
the CROs and Third Party Vendors are in alignment and are delivering per the scope of work Manages and oversees study...This role is not eligible remote, and must be onsite in one of our US office locations. The Senior Clinical Study...
with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.... From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients...
, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays... artery diseases. 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up...
Study Start Up Associate II - Medical Device - Arden Hills, MN ICON plc is a world-leading healthcare intelligence.... Your responsibilities will include: Work independently and proactively to coordinate all necessary activities for site regulatory...