Genpact · 9 hours ago
Technical Project Manager
United States
Contract
Remote
Senior Level, Lead/Staff
$60/hr - $65/hr
8+ years exp
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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
Qualification
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Required
8+ years experience working with life sciences or healthcare companies performing system implementation experience either as a consultant, business, or IT representative
In-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing and/or Viewing systems
Proven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfaction
Influential; experience leading teams through hard decisions and negotiating compromises
Technical abilities and willingness to “roll up your sleeves” to design and implement a RIM solution
Expert on life sciences compliance and computer systems validation requirements
Ability to work independently in a dynamic environment
Typical travel is 25% but may be up to 50% based on customer requirements
Preferred
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, etc.
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)
Company
Genpact
Genpact is an information technology firm that offers business management, artificial intelligence, automation, and cloud services.
10001+ employees
H1B Sponsorship
Genpact has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (178)
2022 (165)
2021 (430)
2020 (479)
Funding
Current Stage
Public CompanyTotal Funding
$400M2024-05-30Post Ipo Debt· $400M
2007-08-10IPO
2004-12-29Private Equity
Leadership Team
Balkrishan Kalra
President and Chief Executive Officer
Nallicheri Vaidyanathan Tyagarajan
President & CEO
Recent News
2024-12-04
Techcircle
2024-12-04
Techcircle
2024-11-28
Company data provided by crunchbase
