Parexel
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Hyderabad · On-site · 5-8 Yrs · Sep 11
Biotech & Pharmaceuticals · 10000+ Employees · Raleigh, US
Parexel is a leading global clinical development partner providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Our 22,000+ professionals design and deliver clinical trials with the patient in mind and With Heart®. Recruitment Fraud Alert It has been brought to our attention that there has been fraudulent activity by scammers attempting to represent themselves as Parexel employees or recruiters. These individuals are attempting to reach potential job seekers through online chat interviews and sending false offer letters, representing Parexel without our consent. If you’re concerned that you’ve been contacted by an unauthorized Parexel recruiter or employee, please notify Jobs@Parexel.com. You may also report suspicious fraudulent activity to your local law enforcement agency. Thank you.
Hiring: Engineering
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Interview experience · Drug Safety Associate
The interview process consists of three rounds. Round 1 is a virtual interview conducted through Doselect, followed by Round 2, which is also conducted virtually via Doselect. Candidates who successfully clear both round
Easy difficulty · India · 172 reports
More interview insightsJob description
Overview
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry.
Responsibilities
- Lead the design, implementation, and management of Data Receipt Agreements with vendors and coordinate with cross-functional teams to establish efficient data transfer protocols
- Program and establish import procedures for data ingestion using SAS, SQL, R, or alternative technologies such as Workbench, ensuring seamless integration of external data sources
- Develop and execute comprehensive reconciliation checks and validation protocols to ensure accurate and complete data transfer across all systems
- Design and program offline listings and custom reports that provide actionable insights to study teams and clients, enabling data-driven decision making
- Aggregate and manage data across multiple sources, handling missing values, raw data files, data structures, and complex programming challenges with precision and accountability
- Review and analyze data outputs to identify patterns, anomalies, and opportunities for improvement, providing strategic insights to enhance study quality and efficiency
- Maintain accountability for first-time quality on all deliverables, ensuring compliance with SOPs, regulatory guidelines, and industry standards including ICH-GCP and 21 CFR Part 11
- Lead and coordinate programming teams to successful project completion within established timelines and budgets, while monitoring resourcing and managing scope changes
- Manage the deployment and optimization of data management technologies including SAS, Workbench, R, and other systems used for creating offline listings and data solutions
- Develop, implement, and maintain technical documentation, data standards, and quality processes that ensure traceability, regulatory compliance, and operational efficiency
- Mentor and provide technical guidance to team members and project teams, fostering a culture of continuous improvement and technical excellence
- Participate in business development activities including bid defense meetings, contributing technical expertise to support new business opportunities
- Advanced technical proficiency in at least one programming language (SAS, SQL, or R) with demonstrated ability to design and implement complex data solutions
- Strong leadership and mentoring capabilities with the ability to motivate and guide virtual teams across multiple time zones and cultures
- Extensive experience working in clinical research or regulated environments with deep knowledge of clinical trial processes and data management best practices
- Excellent communication and interpersonal skills with the ability to translate technical concepts for diverse stakeholders and build strong working relationships
- Demonstrated commitment to first-time quality, methodical problem-solving, and continuous process improvement in complex technical environments
- Comfort working with multiple data management systems and technologies, with the ability to quickly master new tools and adapt to evolving technical landscapes
- Strong analytical and strategic thinking skills with the ability to identify opportunities for efficiency improvements and innovation in clinical trial operations
Qualifications
- Bachelor's degree in a relevant science discipline or equivalent
- Minimum 5+ years of experience in clinical research, data management, or a related field
- Proficiency in at least one programming language (SAS, SQL, or R) with demonstrated expertise in data manipulation and analysis
- Hands-on experience working with at least two clinical data management systems (such as SAS, Workbench, or Elluminate)
- Strong knowledge of ICH-GCP, regulatory requirements, SOPs, system life cycle methodologies, and applicable regulations including 21 CFR Part 11
- Demonstrated leadership experience mentoring team members and managing technical projects
- Excellent written and oral communication skills in English with the ability to present complex technical information clearly to diverse audiences
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Job application FAQ
Last updated 2 October 2026
- How do I apply for Senior Clinical Data Engineer at Parexel?
- Open this job on Feedback AI and sign up free (or sign in). You can apply from the job detail page; match scores and skill gaps appear when your profile is complete. Parexel may attach structured assessments to interview rounds after you apply.
- Does Feedback AI show a match score for this Senior Clinical Data Engineer role?
- Yes after you add a resume or skills. Match score ranks this role against your profile — skills met, gaps, level, and location — so you prioritise applications where fit is strongest.
- Is Senior Clinical Data Engineer remote or on-site in Hyderabad, Telangana (+1 other)?
- This listing is marked on_site with location Hyderabad, Telangana (+1 other). Confirm details on the job description before applying.
- What skills matter for this Senior Clinical Data Engineer role at Parexel?
- This is a senior Senior Clinical Data Engineer role. Key skills include skills listed in the job description. Feedback AI highlights matched vs missing skills on your profile after signup.