Study Associate I / Band B Job Schedule: Candidate must be able to come onsite to Basking Ridge, NJ office 1-4 times... on Harmonization (ICH) guidelines. Key focus is on providing clinical administrative support to study teams and on interacting with the...
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...
Support the Clinical Operations Study Leader and team in managing and overseeing clinical trials. Reports... to an Associate Director of Clinical Operations (or above). Responsibilities: Assist in day-to-day trial execution: site start-up...
Clinical Study Associate ICON plc is a world-leading healthcare intelligence and clinical research organization... and dynamic team as an FSP member of staff, working as a Clinical Study Associate, dedicated exclusively to a Pharmaceutical...
Senior Clinical Study Associate - Contract - Cambridge, MA (hybrid role) Be the backbone of clinical research...-join a team shaping tomorrow's therapies. Proclinical is seeking a Senior Clinical Study Associate for a hybrid role based...
States Cambridge, USA Posting date: 17 Dec 2025 Reference: 67988 Senior Clinical Study Associate - Contract... is seeking a Senior Clinical Study Associate for a hybrid role based in Cambridge, MA. This is an excellent opportunity...
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...
while transforming your career. Principal IS Business Analyst – Clinical Study Design and Analysis What you will do Let...’s do this. Let’s change the world. Amgen is seeking a Principal IS Business Analyst to join the Clinical Study Design and Analysis...
Clinical Study Manager ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re.... Working as a Clinical Study Manager, exclusively assigned to a Pharmaceutical Company, you will lead or support PTA (Post...
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...
Senior Associate Study Manager ICON plc is a world-leading healthcare intelligence and clinical research organization... but not limited to, clinical protocols, consent forms, study guides, monitoring plans, e(CRF)s, subject information sheets, clinical...
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...
Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to assigned... field (Master’s preferred). 7+ years of experience in clinical research, project management, or study operations...
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...
Senior Associate Study Manager ICON plc is a world-leading healthcare intelligence and clinical research organization... to support the execution and monitoring of clinical studies and trial deliverables. Participate in study planning and set-up...
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...
. Develop SOPs supporting clinical trial testing as required. Maintain Study Binders/Trial Master File (TMF... with CAP/CLIA/CDx regulatory compliance and quality assurance standards. Minimum of 2 years Study Coordinator or Clinical...