Senior Consultant - Regulatory Operations Software Implementation (Remote)

Veeva Systems; Philadelphia (Philadelphia County); Hybrid; USD 150,000 - 200,000; Full time

Job summary

A leading company in life sciences software solutions is seeking an experienced leader for software implementation projects, particularly in the regulatory space. This role involves direct collaboration with large pharmaceutical firms and emerging biotechs, ensuring successful project execution and high stakeholder satisfaction. The ideal candidate will possess extensive experience in system implementations and strong technical knowledge in regulatory information management, with opportunities for growth and flexible work options.

Benefits

Comprehensive benefits package

Flexible work-from-home options

Opportunity for career advancement

Supportive work environment

Commitment to charitable giving

Qualifications

• 8+ years of experience in system implementation within life sciences.
• In-depth knowledge of drug development processes and regulatory submissions.
• Proven leadership in complex decision-making and negotiations.

Responsibilities

• Lead software implementation projects at life sciences companies.
• Design and implement solutions using the Vault Regulatory suite.
• Serve as the primary customer liaison for effective stakeholder communication.

Skills

Project Management

Stakeholder Collaboration

Technical Design

Education

Degree in Life Sciences, Computer Science, or related field

Tools

Veeva Vault

Job description

Employer Industry: Life Sciences Software Solutions

Why consider this job opportunity:
- Salary up to $200,000
- Opportunity for career advancement and growth within the organization
- Flexible work-from-home options available
- Comprehensive benefits package including medical, dental, vision, and basic life insurance
- Supportive and collaborative work environment with a focus on employee success
- Commitment to charitable giving through a 1% charitable giving program

What to Expect (Job Responsibilities):
- Lead software implementation projects at life sciences companies, including both large pharmaceutical firms and emerging biotechs
- Design and implement solutions using the Vault Regulatory suite
- Conduct configuration requirements workshops and document content solutions
- Manage program and project activities, including resource planning and team leadership
- Serve as the primary customer liaison, ensuring effective communication between stakeholders

What is Required (Qualifications):
- 8+ years of experience in system implementation within life sciences or healthcare
- In-depth knowledge of drug development processes and regulatory submissions
- Proven ability to collaborate with diverse stakeholders and ensure high satisfaction delivery
- Experience leading teams through complex decisions and negotiations
- Technical skills for designing and implementing regulatory information management solutions

How to Stand Out (Preferred Qualifications):
- Experience with systems such as Veeva Vault, PAREXEL/LIQUENT InSight, or other regulatory information management systems
- Background in Regulatory Affairs, Regulatory Operations, or Pharmacovigilance
- PMP certification or experience with Agile methodology
- Degree in Life Sciences, Computer Science, or a related field
- Locality to major life sciences customer hubs (e.g., NJ, Boston, San Francisco)

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