TRABAJO REGULATORY AFFAIRS CLINICAL WRITING MADRID, MADRID

You’ll gain exposure to various therapeutic areas and clinical study types, creating an excellent foundation for growth in global clinical operations, regulatory...

· regulatory compliance (change control, post-approval activities, etc... )· interactions with key business partners and regulatory authorities· launch or supply...

Knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

), protection (medical errors/patient safety, clinical trials, etc... experience with health care, business national/ regional legislative and executive branch regulatory...

Conduct regulatory intelligence gathering to support development of regulatory roadmaps, complex feasibility assessments, and other regulatory intelligence reports...

• superior clinical research operational knowledge... • proficient in speaking and writing local country language and english... task: • services rendered will adhere...

Collaborates with local medical affairs team... excellent understanding of the clinical study process including monitoring... works together with regulatory affairs...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards... we create intelligent connections...

Hospitals & government affairs kols... functional relationships internal project management function within astrazeneca cross functional project teams marketing...

This role is ideal for someone who thrives at the intersection of privacy, regulation, and clinical research... demonstrated experience in information governance...

Good understanding of clinical trial contract management... strong legal, financial and/or technical writing skills... qualifications   bachelor's degree related...

Design, develop, troubleshoot and improve next generation software for use in clinical research and clinical applicationsâ ... follow quality and regulatory guidelines...

Advise on regulatory interactions, support successful management of regulatory examinations and requests; conduct regulatory horizon scanning...

Design, develop, troubleshoot and improve next generation software for use in clinical research and clinical applications... follow quality and regulatory guidelines...

At least 1 year of medical affairs or msl experience...       synthesize complex data and effectively communicate meaningful clinical insights and unanswered customer...

Understands regulatory guidelines and landscape... scientific expertise (nice to have) has deep knowledge of ta/product, clinical landscape...

Iqvia is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries...