Senior Principal Consultant

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(R).

About the Role

We are seeking a Senior Principal Consultant to join our team. As a consultant, you will drive the delivery of comprehensive drug safety solutions that protect patient well-being and ensure regulatory compliance. This position plays a key role in designing and implementing pharmacovigilance strategies, managing complex safety data, and providing expert guidance to clients on emerging safety issues and regulatory requirements. You'll collaborate with cross-functional teams, apply industry-leading methodologies, and contribute to the successful execution of pharmacovigilance programs from initiation through ongoing monitoring.

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through advanced drug safety solutions and strategic client partnerships. With diverse teams and continuous learning opportunities, the Pharmacovigilance Consulting Services Lead can explore career paths and expand expertise across clinical research, regulatory affairs, and data analytics.

Key Responsibilities

Analyze business needs and provide strategic guidance to ensure drug safety solutions meet customer objectives and drive successful project outcomes

Lead solution design and implementation for client engagements, ensuring high-quality, integrated software solutions delivered within project constraints of time and budget

Serve as a subject matter expert and thought leader, providing technical expertise in drug safety systems including Argus Safety , Insight, Mart, Analytics, OBIEE, and Axway EDI platforms

Manage and mentor a team of technical consultants and developers, providing coaching, guidance, and feedback to develop team member skills and drive project success

Present and demonstrate solutions to customers, influencing customer management in acceptance of solutions and ensuring successful business implementation

Apply hands-on technical expertise in SQL and PL/SQL with strong troubleshooting skills across Argus, Axway, and associated modules to resolve complex technical challenges

You'll thrive in this role if you bring:

Strategic thinking and technical leadership capabilities to guide complex drug safety implementations

Deep experience in drug safety systems, implementation methodologies, and best practices

Strong SQL and PL/SQL programming skills with excellent troubleshooting and problem-solving abilities

Proven ability to lead teams, mentor consultants, and collaborate effectively across organizations

Excellent communication and presentation skills with the ability to influence stakeholder decisions

Required Qualifications

Bachelor's / master’s degree in computer science, information technology, or any engineering degree

11+ years of experience relevant to this position, including 5 years of consulting experience in drug safety or clinical research

Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes

Experience with pharmacovigilance platforms such as Argus Safety , Insight, Mart, or similar systems

Extensive knowledge of writing SQL queries and PL/SQL code

In-depth knowledge of drug safety application implementation, upgrade, and maintenance

Ability to craft and articulate strategic technology solutions that address complex business challenges

Preferred Qualifications

Experience with E2B(R3) or EDI protocols for adverse event reporting

Familiarity with additional pharmacovigilance analytics and visualization tools

Experience in consulting or client-facing roles within the pharmaceutical industry

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 perfect fit, send them the link to apply!