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Salary
≈ $21k – $46k per year (Estimated)
Location
Remote (India)
Seniority
Senior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 20, 2026. First seen by Alion on Oct 13, 2026. Parexel scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Parexel is a clinical research organisation headquartered in Durham, North Carolina that provides Phase I to IV clinical trial services, regulatory consulting, market access and safety services to biopharmaceutical companies. Founded in 1983 and owned by EQT and Goldman Sachs since 2021, it employs more than 21,000 people, with large teams in the US, Hyderabad, Bengaluru, London, Poland, Romania, Serbia and Bloemfontein. Its openings are mostly for regulatory affairs consultants and associates, clinical research associates, safety technology analysts, clinical trial managers, data and AI engineers, many of them home or office based.

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose - moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®

About the Role

We are seeking a Senior Solution Consultant (Pharmacovigilance Consultant, Drug Safety Solutions Specialist) to join our team. As a Senior Solution Consultant, you will drive the design and delivery of innovative pharmacovigilance and drug safety solutions that advance patient safety and regulatory compliance.

This position plays a key role in solution development, client engagement, pre-award support, and post-award delivery oversight. You'll collaborate with cross-functional teams across sales, delivery, and therapeutic areas, follow industry-standard processes, and contribute to solution development from initial client discovery through successful implementation and account management.

Responsibilities include developing bespoke safety solutions, supporting strategic sales initiatives, and ensuring seamless handovers to delivery teams, with opportunities to deepen your expertise in pharmacovigilance and influence the strategic direction of Parexel's drug safety business.

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through innovative solution design, client-centric consulting, and operational excellence. With diverse teams and continuous learning opportunities, the Senior Solution Consultant can explore career paths and expand skills across clinical research and commercial operations.

Key Responsibilities

  • Lead solution development and design of bespoke pharmacovigilance and drug safety solutions that maximize value for clients and differentiate Parexel in the market
  • Support sales initiatives through strategic guidance, opportunity identification, and participation in client discovery sessions to understand business objectives and system need
  • Develop efficient, competitive, and profitable solutions, including scope definition, budget preparation, and commercial proposals for pre-award and post-award engagement
  • Manage client relationships and provide account oversight to ensure solutions meet expectations for time, cost, quality, and customer satisfaction
  • Maintain extensive knowledge of pharmacovigilance products, pipelines, competitors, and industry trends to position Parexel for competitive advantage and business growth
  • Ensure effective handover of solutions to delivery teams and drive lessons learned feedback loops to achieve continuous improvement
  • Partner with cross-functional teams across enterprise accounts, growth accounts, delivery, and marketing to support SBU-specific sales targets and strategic objectives
  • Develop and present customer-focused, well-articulated proposal content and budgets that clearly communicate Parexel's value proposition and differentiation

Candidate Profile

You'll thrive in this role if you bring:

  • Strengths in strategic thinking, client relationship management, and solution design
  • Experience working in pharmacovigilance, drug safety, clinical research, or a regulated healthcare environment
  • The ability to collaborate across matrix teams, communicate complex ideas clearly, and build strong cross-functional relationships
  • A patient-focused mindset, strong attention to detail, and a pragmatic approach to solving business challenges
  • Comfort working with commercial systems, proposal management tools, and industry-standard processes

Required Qualifications

  • Bachelor's degree in life sciences, pharmacy, health sciences, or related field
  • Minimum 5+ years of experience in Pharmacovigilance, Drug Safety Services, or clinical research
  • At least 2 years of experience in developing and designing client-specific safety solutions or consulting services
  • Proven client-facing experience with strong stakeholder management and consulting skills
  • Knowledge of pharmacovigilance regulations, ICH-GCP, and clinical trial processes
  • Strong communication, organization, and problem-solving skills with demonstrated ability to manage multiple priorities

Preferred Qualifications

  • Advanced degree (Master's or MBA) in life sciences, business, or related field
  • Experience with process improvement methodologies and automation technologies in drug safety or clinical research
  • Active participation in industry forums and professional organizations related to pharmacovigilance
  • Willingness to travel up to 30% as needed for client engagement and business development

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!

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