Act as Medical Reviewer for Veeva AdProm MLR approval processes.
Manage Veeva Vault Medical content and analyze feedback from Global Medical Information.
Build and implement training packages for UCC in collaboration with EMEA Marketing and Business Development teams.
Partner with Public Policy and Market Access teams to integrate medical strategy into broader business initiatives.
Lead KOL mapping, development, and engagement planning across EMEA.
Support clinical studies, publication strategies, and dissemination of real-world evidence.
Assist with product evaluations, clinical documentation, and user training activities.
Utilize tools such as PubMed and regulatory databases for data analysis. Track budgets and oversee administrative processes for timely payments.

Requirements

Advanced degree in medicine, nursing, pharmacy, or life sciences (MD, RN, PharmD, PhD, MSc preferred).
3–5 years in medical affairs within pharma or medical devices, with global exposure.
Strong scientific and clinical expertise in Urology, Infection Prevention, and Critical Care.
Familiarity with European clinical trial requirements, MDR, and ethical standards.
Digital fluency with tools like Veeva Vault, PubMed, and Excel.
Fluent in English (written and spoken) any additional UE languages.

Benefits

Competitive package of compensation and benefits programs

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

medical reviewdata analysisclinical documentationtraining package developmentKOL mappingclinical studies supportpublication strategiesreal-world evidence disseminationbudget trackingadministrative process oversight

Soft skills

collaborationcommunicationleadershipstrategic planninginterpersonal skills

Certifications

MDRNPharmDPhDMSc