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Regulatory Affairs-Senior Manager- English-Remote UK

Genpact

London

Remote

GBP 60,000 - 100,000

25 days ago

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Job summary

An established industry player is seeking a Senior Manager in Regulatory Affairs to lead software implementation projects. This role involves guiding clients through complex software solutions, specifically focused on regulatory information management. The ideal candidate will possess a strong background in consulting and project management, with expertise in systems like Veeva Vault. Join a diverse team dedicated to transforming the regulatory landscape for leading pharmaceutical and biotech companies. This position offers a fantastic opportunity for professional growth and development in a dynamic and supportive environment.

Benefits

Attractive salary

Stable job offers

Professional training

Access to learning platform

Meal Tickets

Medical Services

Insurance

Additional vacation days

Partner discounts

Qualifications

  • Experience in Regulatory Affairs and project management is essential.
  • Bachelor's degree in a relevant field is required.

Responsibilities

  • Lead software implementation projects for life sciences companies.
  • Manage communication between project teams and customers.

Skills

Regulatory Affairs

Project Management

Consulting

Agile Methodology

English Fluency

Education

Bachelor's degree in science or engineering

Advanced degree (preferred)

Tools

Veeva Vault

Salesforce

Oracle

SAP

SharePoint

Documentum

Job description

Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose - the relentless pursuit of a world that works better for people - we serve and transform leading enterprises, including the Fortune Global 500, with our deep business and industry knowledge, digital operations services, and expertise in data, technology, and AI.

Inviting applications for the role of Regulatory Affairs-Senior Manager- English-Remote UK.

We are looking for an experienced candidate with deep expertise in navigating customers through complex software implementation. Veeva's Vault RIM suite is the industry's only unified software solution that provides fully integrated regulatory information management (RIM) capabilities including data and document management, submission publishing, and archival on a single cloud-based platform.

Veeva Systems is looking for consulting leaders with system implementation experience and a passion for helping customers optimize their regulatory data and document management processes.

As a key member of our Professional Services team, the candidate will be responsible for understanding our customers' global regulatory needs, translating requirements into solution design, and defining global strategies for deploying our cloud-based solution for managing regulatory information across the enterprise.

Responsibilities

  • Lead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotechs.
  • Lead the solution design for implementation and use of the Vault Regulatory suite (Vault Registrations, Vault Submissions, Vault Submissions Archive, Vault Publishing).
  • Lead configuration requirements workshops, design, prototype, configure and document content solutions.
  • Program and project management including resource planning, leading, and motivating a cross-functional team.
  • Primary customer liaison managing communication between the project team, customer, and internal stakeholders.
  • Mentor project team and consultants, helping others improve their consulting skills.

Qualifications we seek in you!
Minimum Qualifications / Skills

  • Bachelor's degree required in science, engineering or related field (advanced degree preferred).

Preferred Qualifications/ Skills

  • Direct experience with systems such as Veeva Vault, PAREXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems.
  • Consulting experience, working with a major system integrator or software vendor.
  • Regulatory Affairs, Regulatory Operations, or Pharmacovigilance background.
  • Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data and content.
  • PMP certification.
  • Execution experience with Agile methodology and/or ACP Certification.
  • Life Science, computer science or related degree.
  • SaaS/Cloud experience.
  • Locality to major life sciences customer hub (NJ; Boston, MA; San Francisco, CA; Philadelphia, PA; Chicago, IL).
  • English Fluency.

What can we offer?

• Attractive salary;

• Stable job offers - employment contract;

• Work in a multicultural and diverse environment with employees from over 30 countries;

• Genpact supports professional trainings and great career development opportunities;

• Free access to our award-winning learning platform;

• Benefits such as Meal Tickets, Medical Services, Insurance, additional vacation days or partner discounts.

Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion or belief, sex, age, national origin, citizenship status, marital status, military/veteran status, genetic information, sexual orientation, gender identity, physical or mental disability or any other characteristic protected by applicable laws. Genpact is committed to creating a dynamic work environment that values respect and integrity, customer focus, and innovation. Get to know us at www.genpact.com and on X, Facebook, LinkedIn, and YouTube.

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