TRABAJO REGULATORY START UP SPECIALIST

up to 3 years clinical research experience... perform start up and site activation activities according to applicable regulations, sops and work instructions...

Responsabilities set up and maintain drugdev spark for new projects (i... prepares and manages site regulatory documentation; reviews and negotiates site regulatory...

As a country approval specialist, you are responsible for pulling regulatory country submissions together in order to activate investigative sites...

regulatory agency (ra), central independent ethics committee (iec) and any other central authorities for the assigned country/countries... ideally + 2 years of experience...

\r\n\r\n as a start up lead, you will lead all aspects of start up activities at the regional level to achieve quick and successful activation of sites, overseeing...

\r\n\t ad-hoc member of the core team meeting throughout study start up... \r\n\t partner with clinical trial application and cro start up functions to align all...

This role will see you leading the oversight of study start up activities for assigned studies across europe... freelance study start up lead - eu & us - cro - home...

* provide country specific ssu expertise to study start up team leads and project teams... * a minimum of 3 years of experience or understanding of clinical study...

Study start up associate ii as a member of the study start up team, you will play an integral role in making sure that physicians at our research sites are prepared...

Perform regulatory document for maintenance e... as a study start up associate i at icon, you'll work as a member of the study start up team, you will play an integral...

Perform regulatory document for maintenance e... as a study start up associate i "medical device" at icon, you'll work as a member of the study start up team, you...

start developing business relationships with hospital personnel (e... team up with sales rep to meet existing and potential clients (e... providing intial and continuous...

If you’re up for the challenge, send us your resume and cover letter explaining why you're the best person for the job... identification no...

\r\n\r\n our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field... you will ensure that individual...

Key contact with external regulatory assurance advisors... the legal entity finance (lef) function will appoint a regulatory reporting specialist in spain...

We are seeking a highly motivated individual to join us as a sales specialist... this role will specialize in identifying qualified leads from different marketing...

Job title: global cleaning validation specialist internal title: sr staff quality specialist reporting to: director of global quality operations group/division:...

When you start, you will go through a training program to get up to speed... important! if you do not receive an email from us: first, emails may take up to 15 minutes...

start date: as soon as possible... we are looking for a passionate, dedicated, and skilled product quality assurance specialist who can assist in the evaluation...