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Veeva Systems recherche un Lead Software Implementation pour diriger des projets au sein d'entreprises des sciences de la vie. Ce rôle implique de concevoir et d'implémenter des solutions en utilisant la suite Vault Regulatory. Le candidat idéal disposera d'une expérience significative dans l'implémentation de systèmes et d'une connaissance approfondie des processus réglementaires.
Employer Industry: Life Sciences Software Solutions
Why consider this job opportunity:
- Salary up to $200,000
- Flexible work-from-home options to support your ideal work environment
- Comprehensive medical, dental, vision, and life insurance benefits
- Flexible PTO and company-paid holidays to encourage work-life balance
- Opportunity for career advancement and growth within the organization
- Commitment to charitable giving with a 1% charitable giving program
What to Expect (Job Responsibilities):
- Lead software implementation projects at life sciences companies, from large pharmaceuticals to emerging biotechs
- Design and implement solutions using the Vault Regulatory suite, including configuration and documentation
- Manage program and project resources, ensuring effective team collaboration and motivation
- Act as the primary customer liaison, facilitating communication among stakeholders
- Mentor project team members and consultants to enhance their consulting skills
What is Required (Qualifications):
- 8+ years of experience in system implementation within life sciences or healthcare companies
- In-depth knowledge of drug development processes and regulatory submissions
- Proven ability to collaborate and communicate effectively with diverse stakeholders
- Experience in leading teams through complex decision-making processes
- Technical skills with a hands-on approach to designing and implementing RIM solutions
How to Stand Out (Preferred Qualifications):
- Direct experience with various regulatory information management or submission publishing systems
- Consulting experience with a major system integrator or software vendor
- Background in Regulatory Affairs, Regulatory Operations, or Pharmacovigilance
- Knowledge of regulatory processes in the Pharmaceutical, Biotechnology, or Medical Device sectors
- PMP certification or experience with Agile methodology
#LifeSciences #SoftwareImplementation #RemoteWork #CareerGrowth #ConsultingOpportunity
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