LAVORO REGULATORY AFFAIRS ASSOCIATE LABELING

• may participate during the inspections of the authorities providing regulatory support on topics related to pmf... • prepares pmf regulatory applications in compliance...

Overview: the head emea regulatory affairs strategy organization is a member of the global regulatory affairs organization... other independence/autonomy/reporting...

Reporting relationships: reports to vp head emea regulatory affairs strategy organization... the jobholder ensures a high level of regulatory professionalism that...

Collaborate with cross-functional teams to ensure timely and quality regulatory submissions, including review and approval of regulatory documents and labeling...

Abiomed, part of johnson & johnson's medtech, is recruiting for a senior regulatory affairs specialist... the senior regulatory affairs specialist will be responsible...

Main responsibilities: • supports regulatory project plan execution • maintain awareness of regulatory requirements and ensure continued learning • maintain regulatory...

Essential functions • acts as a regulatory team leader on more complex projects, which may include technical writing; • prepares and\/or reviews regulatory documentation...

Scopri il mondo optima attraverso il sito internet: seguici sui nostri canali social in staff alla divisione regulatory affairs , la risorsa affiancherà il responsabile...

Manpowerprofessional ricerca per importante realtà farmaceutica una figura di regulatory associate appartenente alle categorie protette (art...

La risorsa infatti, rispondendo al responsabile della divisione qa/ra, avrà la possibilità di gestire in piena autonomia i nuovi progetti, partendo dalla redazione...

Plans and travels to national and international annual conference/internal meeting manages the logistical and provide scientific support for medical affairs programs...

Johnson & johnson is recruiting for an associate director, clinical project scientist, oncology...   ability to work 5 days a week fluent in written and...

Experience working with regulatory authorities and/or european notified bodies is preferred...    the position requires good judgement in interpreting...

May act as feasibility associate after appropriate and documented training... guides and supervises clinical research associate i (cra i) in order to coach and train...

Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out... works in partnership internally with...

Plan and conduct monitoring site visits (site qualification visit, site initiation visit, interim monitoring visit, or close-out visit) and regulatory submissions...

Contribute to or lead selection of sites, in collaboration with cdc and local colleagues such as line managers and medical affairs... from health-care-provider interactions...

·         support medical affairs program and activities at local and regional level...       ...

Identify appropriate investigators as defined by study-specific requirements and by the applicable regulatory code... maintain open communication and relationships...