Parexel Statistical Programmer II Recruitment 2026: Apply Online for 1 Vacancies

About the Role

As a member of Parexel’s Statistical Programming group, you will be instrumental in analyzing, summarizing, and graphically presenting clinical data to assess the safety and efficacy of clinical trials. This role demands meticulous attention to detail, a steadfast commitment to quality, and effective communication skills to help ensure new treatments reach patients faster. You will engage with diverse therapeutic areas, analyze various data entries, and operate within an ever-evolving environment. Parexel fosters a fertile ground for growth, offering extensive training, mentoring, and technical knowledge sharing.

You will collaborate closely with clients and internal Parexel teams, leveraging collective strengths. Experience a supportive and motivating work environment where our teams offer an inherent breadth of knowledge within a diverse and inclusive workplace.

Key Accountabilities

• Project Management Assistance: Aid in coordinating project start-up activities, creating global programs, tracking spreadsheets, and other essential documentation.
• Statistical Programming: Deliver high-quality service by producing derived datasets (e.g., SDTM, ADaM), tables, figures, and data listings of varying complexity. Perform Quality Control (QC) on low-to-medium complexity derived datasets, tables, figures, and data listings.
• Documentation Support: Assist in the production and QC of derived dataset specifications and other process-supporting and submission documentation.
• Training and Development: Maintain and expand knowledge of local and international regulatory requirements within the clinical industry. Develop expertise in SAS and Parexel’s internal processes and procedures. Provide relevant training and mentorship to staff and project teams as appropriate.
• General Compliance: Ensure all supporting documentation for studies is maintained in accordance with SOPs/Guidelines to guarantee traceability and regulatory compliance. Adhere to SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations. Participate in internal/external audits and regulatory inspections as required. Proactively contribute to process/quality improvement initiatives. Understand regulatory requirements concerning industry technical standards (e.g., CDISC, 21 CFR Part 11, and electronic submissions).

Skills Required

• Excellent analytical skills.
• Proficiency in SAS.
• Knowledge and understanding of the programming and reporting process.
• Familiarity with SOPs/Guidelines, ICH-GCP, and other applicable local and international regulations such as 21 CFR Part 11.
• Ability to learn new systems and function in an evolving technical environment.
• Capacity to manage competing priorities and flexibility to adapt to change.
• Strong attention to detail.
• Ability to work effectively as part of a global team.
• Capability to work effectively in a quality-focused environment.
• Effective time management skills to meet daily metrics or team objectives.
• Commitment to performing consistently high-quality work.
• Business/operational skills including customer focus, commitment to quality management, and problem-solving.
• Competent in written and oral English.
• Good communication skills.

Parexel is a leading global clinical research organization (CRO) dedicated to advancing the development of new medicines. We partner with pharmaceutical, biotechnology, and medical device companies to help bring life-changing treatments to patients faster. Our expertise spans the entire drug development lifecycle, from early-phase research to regulatory submission and post-market support. We foster a patient-centric culture, driven by a commitment to quality, innovation, and collaboration. At Parexel, we believe in working ‘With Heart,’ prioritizing the well-being of patients and our employees.