LS/Consultant - Junior Project Manager, Life Sciences, Infosys Consulting

erational excellence, and regulatory compliance initiatives.
Here are some engagements our Life Sciences consultants are working on:

• Leading digital transformation programs for global pharmaceutical firms to modernize clinical trial operations and improve patient engagement.

• Implementing regulatory information management systems to streamline compliance and submission processes.

• Driving commercial analytics initiatives to optimize product launch strategies and market access.

• Managing enterprise-wide data governance programs to ensure data integrity across R&D and regulatory functions.

• Coordinating cross-border teams to deploy AI/ML solutions for drug discovery and pharmacovigilance.

• Supporting change management and training programs for global rollouts of life sciences platforms (e.g., Veeva, Medidata, Oracle Health Sciences).

Responsibilities

• Lead end-to-end IT project lifecycle (initiation, planning, execution, monitoring, closure)

• Support program governance, status reporting, risk/ issue tracking, and stakeholder communication

• Collaborate with client stakeholders, internal teams, and third-party vendors to ensure alignment and timely execution.

• Facilitate workshops, status meetings, and steering committee updates with senior stakeholders.

• Manage project documentation, dashboards, and reporting (excel/ PowerPoint)

• Identify risks and mitigation strategies, ensuring compliance with industry regulations (e.g., GxP, FDA, EMA).

• Support business development efforts including proposal creation, client presentations, and solution design.

• Contribute to internal initiatives such as knowledge management, capability building, and thought leadership.

Basic Qualifications

• Bachelor's degree in Life Sciences, Engineering, or related field; advanced degree preferred.

• 3+ years of experience in project management within the life sciences industry or consulting.

• Experience to lead IT projects as project manager in multiple delivery methodologies (e.g. waterfall, agile).

• Location: Dallas, NY, NJ

• Hands-on experience with project management tools (MS project or equivalent)

• Strong excel and PowerPoint skills for reporting and presentations

• Proven track record of delivering complex programs in pharmaceutical, biotech, or medical device sectors.

• Excellent communication, presentation, interpersonal skills, stakeholder management, and problem-solving skills.

• PMP, or Agile certification is a plus.

• Candidates authorized to work for any employer in the United States without employer-based visa sponsorship are welcome to apply. Infosys is unable to provide immigration sponsorship for this role at this time

Preferred Qualifications / Skills

• Familiarity with clinical trial operations, regulatory submissions, pharmacovigilance, or commercial analytics.
• Ability to work across global teams and manage stakeholders in multiple time zones.
• Strong analytical mindset with experience in data-driven decision-making.
• Passion for innovation in life sciences and a commitment to improving patient outcomes.

Along with competitive pay, as a full-time Infosys employee you are also eligible for the following benefits:-

• Medical/Dental/Vision/Life Insurance
• Long-term/Short-term Disability
• Health and Dependent Care Reimbursement Accounts
• Insurance (Accident, Critical Illness , Hospital Indemnity, Legal)
• 401(k) plan and contributions dependent on salary level
• Paid holidays plus Paid Time Off