TRABAJO REGULATORY SPECIALIST STUDY START

study start up associate / contract specialist at icon, it’s our people that set us apart... study start up associate ii as a member of the study start up team,...

study start up associate iias 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...

Prepare site regulatory documents, reviewing for completeness and accuracy... inform team members of completion of regulatory and contractual documents for individual...

Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst...

Protocols/amendments, informed consent form (icf) documents detailing study delivery data management activities, etc... provides matrix management of functional...

• direct the study team in the implementation of audits and regulatory inspections... typical accountabilities • provides operational expertise to the study team...

Manage the following aspects of study progress: start up nominate, approach, and complete qualification processes including establishing site/sponsor expectations...

Support the study team in the implementation of audits and regulatory inspections... support risk management and quality efforts to ensure study compliance...

• experience in all phases of a clinical study lifecycle... • extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities...

Description: we have an open position for a lead regulatory associate to join our regulatory unit within the clinical operations department...

With regulatory agencies to ensure compliance with safety-related regulations... clinical research protocols and investigate any potential safety risks associated...

• knowledge of relevant regulatory agency standards... • supports the technical services team in audits/inspections from regulatory agencies and pharmaceutical sponsors...

\u knowledge of relevant regulatory agency standards... \u supports the technical services team in audits\/inspections from regulatory agencies and pharmaceutical...

Complex complaint specialist location: stoke on trent / hybrid   (blended home working)    onsite a minimum 8 days per month at the stoke on trent contact centre ...

Continuously expand your market and domain knowledge and be at the forefront of new strategic initiatives and regulatory drivers to influence the future direction...

Follow up customer behavior evolution trends ensure all products to be conform with the evolution of the regulatory requirements on their distributionfollow day...

Detailed study of packaging behavior during transport... providing input on manufacturability and costs, providing trial testings in order to obtain the best product...

Manages study supplies (isf, etc), drug supplies and drug accountability at study site... prepares study drug for destruction, if applicable... ensures timely collection/uploading...