Preparing for an interview at Pra Health Sciences requires a dual focus on your technical expertise and your professional adaptability. You should approach your preparation not just as an academic exercise, but as a demonstration of how you can deliver high-quality scientific results within a commercial, client-driven framework.

Role-Related Knowledge – You must demonstrate a deep, hands-on understanding of the specific scientific methodologies and instrumentation relevant to the team you are joining. Be ready to explain the "why" behind your experimental designs, rather than just listing the techniques you have used.

Regulatory and Compliance Mindfulness – At Pra Health Sciences, scientific integrity is non-negotiable. Interviewers will closely evaluate your commitment to GLP/GCP standards, your meticulousness in documentation, and your understanding of quality control processes.

Adaptability and Project Management – The CRO environment is dynamic, with shifting client priorities and strict deadlines. You need to show that you can maintain scientific rigor and composure when managing multiple projects simultaneously.

Communication and Panel Presence – Because you will be presenting to internal stakeholders and external clients, your ability to articulate scientific concepts clearly and confidently is critical. You must show that you can collaborate effectively with diverse teams.

The interview process at Pra Health Sciences is structured to evaluate both your cultural fit and your technical capability. While candidates generally describe the initial stages as highly conversational and welcoming, the process becomes progressively more rigorous as you move toward the final rounds.

The typical journey begins with an informal conversation with an internal recruiter, followed by a more structured video or phone interview with the hiring manager, and culminates in a comprehensive panel interview.

The timeline above outlines the typical progression from the initial recruiter screen to the final decision. Candidates should use this timeline to pace their preparation, ensuring they are fully ready for the technical depth of the final panel by the time the video screen is complete. While the early stages move relatively quickly, the coordination of the onsite or virtual panel can take time, so maintaining communication with your recruiter is key.

To stand out during the hiring process, you must understand the specific competencies that the interview panel will be evaluating. Your interviewers—consisting of senior scientists and managers—will look for a balance of technical mastery and operational efficiency.

Assay Validation and Bioanalysis

This area evaluates your core laboratory competency and your ability to generate reliable, reproducible data. The team wants to ensure you can join the lab and contribute immediately with minimal oversight.

Be ready to go over:

• Method Development – The step-by-step process of designing a novel assay from scratch.
• Validation Parameters – How you assess accuracy, precision, selectivity, sensitivity, and stability.
• Troubleshooting Protocols – Your systematic approach to identifying and fixing instrument drift, matrix interference, or reagent issues.
• Advanced concepts (less common) – High-throughput automation, multiplexing assay platforms, and advanced pharmacokinetic/pharmacodynamic (PK/PD) modeling.

Example questions or scenarios:

• "If your calibration curve shows poor linearity at the lower limit of quantitation, what parameters would you adjust first?"
• "Describe a time you successfully transitioned a manual assay to an automated liquid-handling platform."

GLP/GCP Regulatory Compliance

Working at Pra Health Sciences means your data will be submitted to global regulatory agencies. Interviewers must be completely confident in your commitment to compliance and quality assurance.

Be ready to go over:

• SOP Adherence – Your experience writing, reviewing, and strictly following standard operating procedures.
• Audit Readiness – How you organize your laboratory notebooks and electronic records to withstand intense regulatory scrutiny.
• Deviation Management – The formal process of documenting, investigating, and implementing corrective and preventive actions (CAPA) when errors occur.

Example questions or scenarios:

• "Walk us through how you would document an unexpected instrument failure mid-run under GLP guidelines."
• "What steps do you take to verify the calibration status of your laboratory equipment before beginning a critical study?"

Client and Project Management

As a scientist in a CRO, you are ultimately delivering a service to a client. You must show that you understand the business side of science, including timelines, deliverables, and relationship management.

Be ready to go over:

• Milestone Tracking – How you monitor project progress against contractually agreed-upon timelines.
• Client Communication – Your strategy for delivering bad news (e.g., a failed assay or a delayed timeline) while maintaining a positive client relationship.
• Cross-functional Collaboration – How you work alongside project managers, data managers, and quality assurance officers to streamline project delivery.

Example questions or scenarios:

• "How would you handle a situation where a sponsor requests a change to the study protocol that conflicts with our internal SOPs?"
• "Describe how you manage your daily workload when three different client projects require your attention simultaneously."

As a Research Scientist at Pra Health Sciences, your day-to-day activities will be dynamic and highly structured. You will spend a significant portion of your time in the laboratory, but your responsibilities extend far beyond bench work to encompass study design, data analysis, and cross-functional communication.

Your primary responsibilities will include:

• Designing, validating, and executing bioanalytical methods to support clinical and non-clinical studies.
• Analyzing complex datasets using specialized scientific software and preparing comprehensive technical reports, study protocols, and SOPs.
• Serving as the scientific lead on assigned projects, ensuring all laboratory work is conducted in strict compliance with GLP, GCP, and other applicable regulatory standards.
• Troubleshooting assay performance issues and instrument malfunctions to minimize study downtime.
• Collaborating closely with project managers and principal investigators to ensure project milestones are met on time and within budget.
• Presenting scientific findings and study updates to internal leadership teams and external pharmaceutical sponsors.

The qualifications required for this position depend on the specific level of the role, such as Scientist I or Scientist III. However, all candidates must demonstrate a strong foundation in laboratory sciences and a clear understanding of the CRO industry.

• Must-have skills – Strong hands-on experience with core analytical techniques (such as chromatography, mass spectrometry, ligand-binding assays, or molecular biology methods); deep familiarity with GLP/GCP regulations; and proficiency in scientific data analysis software.
• Nice-to-have skills – Prior experience working in a fast-paced CRO environment; experience with laboratory automation and liquid-handling systems; and client-facing project management experience.

For a Scientist I position, Pra Health Sciences typically looks for a Bachelor's or Master's degree in a relevant scientific discipline (Chemistry, Biochemistry, Biology, or Pharmacology) with 1–3 years of laboratory experience.

For a Scientist III position, the expectation is typically a Ph.D. with several years of post-doctoral or industry experience, or a Master's degree with 5+ years of proven industry experience, demonstrating a track record of independent study design and scientific leadership.