Support groundbreaking clinical trials-join us as a Clinical Study Associate and help ensure quality, compliance..., and innovation in every step. R&D Partners is seeking a Clinical Study Associate I to assist in the planning and execution...
: United States Cambridge, USA Posting date: 08 Jan 2026 Reference: 68099 Clinical Study Associate - Contract - Remote... a global impact. Proclinical is seeking a Clinical Study Associate to support the execution of clinical trials. Primary...
Our client is looking to add a Senior Clinical Study Associate to their team on a contract basis. Responsibilities... in support of the Clinical Study Manager and other team members Prepare study documents (i.e. consent forms, site instructions...
. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team...
Clinical Study Manager provides guidance and oversight to internal and external project team members for the.... Resolves escalated study conduct issues and provides clinical responses to questions from study centers and institutional...
Clinical Trial Associate (Clinical Study Administrator) ICON plc is a world-leading healthcare intelligence... and maintenance of study documents, ensuring template and version compliance. Creates and/or imports clinical-regulatory documents...
on , , , , and . Job Description The Associate Director, Global Study Start Up Transformation Lead, is responsible for supporting the Director... Required: Bachelor's degree in a healthcare or scientific field. Minimum of 7 years of clinical project management and global study...
Study Start Up Associate - Arden Hills, MN ICON plc is a world-leading healthcare intelligence and clinical research.... Preferred Qualifications Research Coordinator or In-House Clinical Research Associate / Clinical Research Associate /Study...
Associate /Study Start up specialist experience. Experience working with clinical trial management systems (e.g., Siebel CTMS...Study Start Up Associate II - Medical Device - Arden Hills, MN ICON plc is a world-leading healthcare intelligence...
Associate /Study Start up specialist experience. Experience working with clinical trial management systems (e.g., Siebel CTMS...Study Start Up Associate II - Medical Device - Arden Hills, MN ICON plc is a world-leading healthcare intelligence...
to join our team as a Research Data Associate - Women and Children Health Study - Mineola. In this role, the successful Research Data... Associate will support several projects relating to the impact that environmental factors have on children's health...
Ops Supervisor, the Study Team Associate is responsible for supporting all study management roles within Clinical... research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out...
otherwise intractable classes of proteins as drug targets. Position: We are seeking an Associate Director, Study Start-Up... to join our Clinical Operations team. In this role, you will support the Eikon Therapeutics portfolio of studies and lead study, country...
required to conduct single and multisite clinical research including study/project management, human subjects' protection, and regulatory... only on official, secure websites. MENU Sign out Sign out Health Science Specialist - Research Study Coordinator...
Reporting to the Clinical Operations Manager and in the Lineberger Comprehensive Cancer Center (LCCC), this position... clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. This position...
advances to patients who live with genetic diseases. The Associate Director (AD)/ Director (D), Global Study Operations..., clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market...
VARITE is looking for a qualified Client Services Study Coordinator in West Sacramento, CA. WHAT THE CLIENT DOES...? An American-headquartered life science and clinical research company. It is a global supplier of analytical instruments, clinical...
SUMMARY: This position will support coding operations and compliance as part of the Modernization Study Program. The... Revision, Clinical Modification (ICD-CM), procedural coding, healthcare common procedure coding system (HCPCS)/current...
of the role proficiently. Minimum 2 years of study coordinator experience . Associate must be based in Santa Fe... lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance...
Integrated Study Timeline Implementation Manager ICON plc is a world-leading healthcare intelligence and clinical..., you will lead development, customization, and maintenance of the Integrated Study Timelines (IST) for clinical trials using global...