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Senior Manager, Clinical Trial Disclosure – Transparency
Genmab. Manage, track, and maintain overall responsibility for disclosure of clinical trial protocols and results on ClinicalTrials.gov, EU CTIS, and other applicable registries/platforms .
Posted 10/14/2026full-timeRemote • New Jersey • United StatesSenior💰 $132,800 - $199,200 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial disclosure management, ensuring compliance with industry guidelines and effective communication across teams. Proficient in leading projects, training staff, and maintaining transparency in clinical trial results.
Highest-signal resume keywords
Clinical Trial Disclosure ExperienceKnowledge Of Disclosure RequirementsProject LeadershipCross-Functional CollaborationExcellent Written And Verbal Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial Protocol ManagementResults Summary DevelopmentSOP UpdatingProcess ImprovementVendor Performance Oversight
Soft Skills
Effective CommunicationRespectful InteractionTraining Delivery
Tools & Technologies
ClinicalTrials.govEU CTISDisclosure Platforms
Industry Keywords
Clinical TrialTransparency DeliverablesCRO LiaisonPlain Language SummariesRegulatory Compliance
About the role
Key responsibilities & impact- Manage, track, and maintain overall responsibility for disclosure of clinical trial protocols and results on ClinicalTrials.gov, EU CTIS, and other applicable registries/platforms
- Support and provide guidance on redaction activities
- Ensure development of plain language results summaries
- Stay updated on industry guidelines to ensure compliance
- Support updating SOPs, contribute to process improvements, and maintain adherence to established standards
- Oversee vendor performance related to transparency deliverables
- Liaise with clinical CROs to ensure consistent messaging across study registries
- Deliver training on Genmab's disclosure processes to internal staff and provide guidance to CROs and vendors
- Ensure internal teams are informed of updated or new requirements and laws
- Manage unsolicited requests received via the clinicaltrials@genmab.com mailbox
Requirements
What you’ll need- 5+ years of clinical trial disclosure experience
- Bachelor's or Master's degree with relevant specialization
- Strong knowledge of disclosure requirements, technology, and platforms
- Proven ability to lead projects and facilitate cross-functional collaboration
- Excellent written and verbal communication that is effective, respectful, and concise
- Previous experience as a Medical Writer is advantageous
Benefits
Comp & perks- 401(k) Plan: 100% match on the first 6% of contributions
- Two medical plan options (including HDHP with HSA), dental, and vision insurance
- Critical illness, accident, and hospital indemnity insurance
- Paid vacation, sick leave, and holidays
- 12 weeks of discretionary paid parental leave
- Access to child and adult backup care
- Family support programs
- Financial wellness tools
- Emotional well-being support
- Commuter benefits
- Tuition reimbursement
- Lifestyle Spending Account for wellness and personal expenses
- Discretionary bonuses and long-term incentives may be available for eligible positions