Lavori presso Genmab

“Genmab seeks a Research Associate for Documentation to support CMC Product Development. The role involves writing scientific documents for regulatory filings, collaborating with cross-functional teams, and optimizing processes. A temporary 9-month position covering a leave of absence, with no expected extension. Requires a background in biochemistry or related fields, strong scientific writing skills, and experience in antibody development. Good English communication skills are essential. Relocation support is not available.”

“Temporary 9-month Associate, Development Materials role at Genmab. Responsible for QC analyses, documentation, and collaboration in antibody development. Requires MLO/HLO degree, lab experience, and English proficiency. No relocation support. Start date May or June.”

“Genmab seeks a Manager, Site Contracts to lead Clinical Trial Agreements (CTAs), FMV negotiations, and payment processes. The role ensures legal and regulatory compliance, manages documentation, and communicates with stakeholders. Requires 5+ years of experience in biotech/pharma, strong contract negotiation skills, and familiarity with GCP, ICH, and FDA/EMA guidelines. Passion for Genmab's purpose and collaborative mindset are essential.”

“Genmab seeks an experienced SAP Security Expert to enhance security controls in a regulated pharma/biotech environment. The role involves SAP GRC, SAP S/4HANA, and compliance with GxP, SOX, GDPR. Responsibilities include user administration, access control, audits, and documentation. Requires 5-7 years of SAP Security experience, preferably in regulated industries.”