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Manager, Statistical Programming

Parexel
Parexel
8-10 years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Manager – Statistical Programming

Location: Hyderabad, India
Employment Type: Full-Time, Permanent
Department: Statistical Programming / Clinical Data Analysis
Company: Parexel


About Parexel

Parexel is a leading global Contract Research Organization (CRO) delivering Phase I–IV clinical development services to pharmaceutical, biotechnology, and medical device companies worldwide. Our Statistical Programming group plays a critical role in analyzing, summarizing, and visualizing clinical trial data to support safety, efficacy, and regulatory decision-making. With a culture of mentorship, knowledge sharing, and technical excellence, Parexel offers a dynamic environment for professional growth in multiple therapeutic areas.


Role Overview

The Manager – Statistical Programming will oversee and guide a team of statistical programmers, ensuring high-quality, timely deliverables across global clinical trials. The role combines team leadership, client interaction, and technical oversight, providing a unique opportunity to influence the delivery of complex programming solutions while mentoring and developing junior staff.

This position requires strong project management skills, clinical trial expertise, and experience leading multi-disciplinary teams in a global, matrixed environment.


Key Responsibilities

Team & Project Leadership:

  • Lead, manage, and mentor a team of statistical programmers, ensuring optimal resourcing and high-quality deliverables

  • Oversee team assignments, project timelines, and productivity metrics to meet departmental and client expectations

  • Facilitate technical guidance and training to support skill development and operational efficiency

  • Conduct formal performance reviews, goal setting, and career development discussions for direct reports

Client & Stakeholder Management:

  • Act as primary liaison with clients, sponsors, and internal project teams regarding project status, technical queries, and deliverables

  • Participate in project bids, client presentations, and strategic planning activities

  • Ensure team adherence to client requirements, regulatory standards, and quality metrics

Operational & Technical Oversight:

  • Review, validate, and monitor project deliverables, including programming outputs, QC documentation, and reporting metrics

  • Ensure compliance with internal SOPs, corporate policies, and global clinical data standards

  • Lead process improvement initiatives to enhance efficiency, accuracy, and consistency across projects

  • Provide input on budgeting, resourcing plans, and project risk management

Strategic Contribution:

  • Support business development activities through client networking, presentations, and generating leads

  • Collaborate with cross-functional teams to drive innovation in statistical programming methodologies

  • Participate in global initiatives, system improvements, and departmental projects


Experience & Qualifications

Required:

  • Bachelor’s degree in Biological Sciences, Pharmacy, Life Sciences, or a related clinical or business discipline

  • Minimum 8–10 years of experience in statistical programming, clinical data management, or related clinical research

  • Proven experience managing teams, projects, and client interactions in a matrixed, global environment

  • Strong expertise in clinical trial data analysis, visualization, and statistical programming

  • Excellent communication, interpersonal, and presentation skills

  • Proficiency in relevant software: SAS, R, SQL, Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)

Preferred:

  • Experience with multi-therapeutic area clinical trials and regulatory submissions

  • Ability to lead and manage a virtual global team across time zones

  • Familiarity with project resourcing, budgeting, and operational metrics in a CRO setting

  • Strong analytical, problem-solving, and negotiation skills


Why Join Parexel Hyderabad

  • Global Exposure: Work on cutting-edge clinical trials with international teams and top-tier sponsors

  • Leadership Growth: Opportunities to lead, mentor, and develop high-performing teams

  • Professional Development: Extensive training, knowledge sharing, and career advancement pathways

  • Collaborative Culture: Inclusive and supportive work environment fostering innovation and teamwork


SEO & GEO Keywords

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