LAVORO REGULATORY AFFAIRS PHARMA CRO

We’re looking for a  senior regulatory affairs manager  to lead and support regulatory activities across europe... senior regulatory affairs manager (remote - eu/uk) ...

regulatory affairs specialist - pharmaceutical company regulatory - pharma azienda our client, a leading pharmaceutical company, is looking for a regulatory affairs...

regulatory & quality manager – esserre pharma | formello (rm)  esserre pharma | nutrienti mediterranei, per la vita...  responsabilità principali regulatory affairs:...

regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...

Ensure cpms maintain compliance with internal sops, gcp, and regulatory standards... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements...

Experience required pharma & data expertise (7+ years): proven experience in data architecture, data engineering ideally within pharmaceutical r&d or life sciences...

• experience in clinical research experience in the pharmaceutical industry or cro... deliverables: • services rendered will adhere to applicable sponsorsops, wis...

Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...

Leverage advanced analytics to validate biomarkers and support their integration into clinical trials, ensuring alignment with regulatory requirements for pharmacodynamic...

Make your mark for patients to strengthen our access sustainability and public affairs (aspa) department we are looking for a talented profile to fill the position...

Main responsibilities leadership: inspire and engage the msl team while fostering a high-performance culture act as a role model of scientific excellence and compliance...

Education scientific degree (biology, biotechnology, pharmaceutical chemistry and technologies, pharmacy, veterinary, or similar discipline) with at least three...

Experience required pharma & data expertise (7+ years): proven experience in data management, governance, metadata & knowledge management ideally within pharmaceutical...

Make your mark for patients   to strengthen our  access, sustainability and public affairs (aspa)  department, we are looking for a talented profile to fill the...

• accountable for submitting proper applications/documents to regulatory authorities and/or iec/irb during the start-up period... • ensure timely collection/uploading...

You will manage study supplies, perform monitoring visits, and prepare for audits and regulatory inspections... essential skills/experience - scientific degree equivalent...

Attends kick-off meetings, weekly team meetings, and client meetings, as needed or requested... specialty board certification required (rheumatologist)...