TRABAJO DIRECTOR STUDY START CIUDAD DE MÉXICO, CIUDAD DE MÉXICO
(33 ofertas de trabajo)
Listado de trabajos de Director study start en Ciudad de méxico, Ciudad de méxico
Study start up associate (i, ii and senior)
We are currently seeking a senior study start up associate to join our diverse and dynamic team... as a senior study start up associate at icon, you will be working...
Study start up associate i (regulatory submissions)
We are currently seeking a study start up associate i to join our diverse and dynamic team... supporting study teams in the development of study documents, including...
We are looking for someone with informed consent form review experience (icf reviewer) to join our study start up group... our study start up associates are integral...
Study start up associate i & ii (site activation associate)
Participate to internal study reviews with study teams to contribute to risk identification and contribute to action planning... study start up associate i & ii...
Participate to internal study reviews with study teams to contribute to risk identification and contribute to action planning... study start up associate i - site...
study team meetings, monitors’ meetings, investigators’ meetings... clinical study administrator base: cdmx esquema de trabajo hibrido the clinical study administrator...
Director, product development- alcohol ready to drink category
Compensation & benefits: competitive benefits package that start on day one of employment... outperforms her/his peers... partner with gdi r&d tech center alcoholic...
Regulatory & start up specialist i, us support, cfsp
Regulatory & start up specialist, cfsp - us support mexico - full home based role purpose: the rsu specialist 1 proactively drives and executes all start up and...
What you will bring: you will play a key role in independently assisting the team to ensure the most effective and efficient study start up, by providing administrative...
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Clinical trial manager sponsor dedicated with 1 year of experience as ctm-home based mexico cdmx
This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and quality assurance (qa)... • oversees site interactions...
study files, crfs, etc... study files, crf files, monitoring files, etc... log in, tracking, quality control as appropriate for the study to share responsibility...
study monitor, investigator contracts lead, site activation partner, clinician, etc... maintain regular communications with investigator sites to gather status updates...
*defines project scope, including resource requirements and deliverables, from a study start up perspective... some responsibilities: *primary study start up point...
¢ delivery of projects in accordance with the contract, timelines and study budget* ⢠identification and review of change orders for the budget ⢠attend and...
Senior servicenow qa and ops developer
Great journeys start here, apply now!... purpose of the role under the general direction of the director of client services, the qa specialist and technical operations...
Principal clinical data science lead
The principal cdsl will provide input into crf design, protocol review, edit check specifications, data entry conventions, monitoring guidelines, and any other study...
Great journeys start here, apply now!... position summary under the general direction of the director of client services, the candidate will lead improvement initiatives...
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