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...
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 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...
-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...
, 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...
of previous study coordination or clinical research coordination experience Analytical skills sufficient to work and solve... while ensuring strict adherence to study protocols and regulatory requirements, including institutional policies, FDA regulations...
, 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...
Are you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team... at Labcorp as a Senior Regional Companion Diagnostics (CDx) Study Manager II. The Senior Regional CDx Study Manager II leads...
VARITE is looking for a qualified Client Services Study Coordinator in West Sacramento, CA. WHAT THE CLIENT DOES..., technical, and non-technical staff augmentation and talent acquisition services. Job Title: Client Services Study Coordinator...
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...
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...
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...
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...
, 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...
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... 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... at a CRO in Study Start-Up Project management experience and demonstrated role in developing others Strong oral and written...
must have legal authorization to work in the United States. Clinical Study Associate I / Band B Assist in planning and execution...Support groundbreaking clinical trials-join us as a Clinical Study Associate and help ensure quality, compliance...