Head- Scientific & Statistical Reporting

MS CLINICAL RESEARCH; Bengaluru; On-site; INR 3,500,000 - 5,500,000; Full time

Job summary

MS Clinical Research in Bengaluru is seeking a strategic Head – Scientific & Statistical Reporting to lead the end-to-end scientific reporting and data analytics function. You will oversee report generation, data interpretation, and statistical reporting for sponsors and internal stakeholders.

The role requires 10–12 years of experience in scientific reporting, biostatistics, or medical writing, with a track record of leading data teams and ensuring high-quality, compliant deliverables.

Qualifications

• 10–12 years of experience in Scientific Reporting, Clinical Data Analytics, Biostatistics, or Medical Writing.
• Strong experience in scientific/study report writing and clinical data interpretation.
• Proven leadership of data/reporting teams.

Responsibilities

• Lead scientific and statistical reporting across clinical studies and research projects.
• Oversee preparation, review, and finalization of scientific reports and summaries.
• Ensure reports are data-driven, accurate, and compliant with sponsor/regulatory expectations.
• Develop standardized reporting templates, workflows, and quality benchmarks.
• Mentor and manage Data Analysts and reporting professionals.

Skills

Leadership

Biostatistics

Medical Writing

Data Analytics

Stakeholder Management

Project Management

Attention to Detail

Report Writing

Tools

Excel

SQL

Power BI

Tableau

Python

Job description

Job Title: Head – Scientific & Statistical Reporting

Experience: 10–12 Years
Department: Scientific & Statistical Reporting / Clinical Data Analytics
Location: Domlur, Bangalore
Reporting To: Director

Role Overview

We are seeking an experienced and strategic Head – Scientific & Statistical Reporting to lead the scientific reporting and data analytics function at MS Clinical Research. This leadership role will be responsible for overseeing end-to-end scientific report generation, interpretation of clinical/study data, statistical reporting, and management of the Data Analytics team. The ideal candidate will possess strong expertise in clinical/study data interpretation, scientific writing, statistical reporting methodologies, and team leadership. This role will lead a team of Data Analysts and ensure the delivery of high-quality, accurate, and scientifically robust reports for sponsors, investigators, and internal stakeholders.

Key Responsibilities

1. Scientific & Statistical Reporting Leadership
   Lead the overall scientific and statistical reporting function across clinical studies and research projects
   Oversee preparation, review, and finalization of scientific reports, analytical summaries, and study outcome documents
   Ensure reports are scientifically accurate, data-driven, and aligned with sponsor and regulatory expectations
   Develop standardized reporting templates, workflows, and quality benchmarks
   Interpret clinical and study data to derive meaningful scientific insights and conclusions
   Ensure consistency, clarity, and scientific integrity in all reporting deliverables


2. Team Leadership & People Management
   Lead, mentor, and manage a team of Data Analysts and reporting professionals
   Allocate projects and reporting responsibilities across the team effectively
   Provide technical guidance on data interpretation, reporting methodologies, and analytical approaches
   Build a high-performance, collaborative, and learning-oriented team environment
   Conduct performance reviews, coaching sessions, and career development planning
   Support hiring, onboarding, and capability development of team members


3. Data Analysis & Interpretation
   Review and interpret complex clinical/study datasets for reporting purposes
   Collaborate with Data Analytics teams to ensure data accuracy, completeness, and reliability
   Apply statistical concepts and analytical methodologies for scientific interpretation
   Identify trends, patterns, and clinically relevant findings from study data
   Ensure appropriate data visualization and presentation within reports
   Work closely with study teams to resolve data inconsistencies and reporting gaps


4. Project & Stakeholder Management
   Manage end-to-end execution of scientific reporting projects within defined timelines
   Coordinate with sponsors, investigators, medical teams, and cross-functional stakeholders
   Act as a key point of contact for reporting-related discussions and deliverables
   Present study findings, summaries, and analytical insights to stakeholders when required
   Ensure timely delivery of high-quality reports aligned with project milestones


5. Quality, Compliance & Documentation
   Establish quality control processes for scientific and statistical reporting
   Ensure compliance with applicable clinical research, GCP, and data governance standards
   Maintain high standards of documentation accuracy, version control, and confidentiality
   Review reports for completeness, consistency, and scientific validity prior to submission
   Continuously improve reporting standards, processes, and operational efficiency

Required Skills & Qualifications

• 10–12 years of experience in Scientific Reporting, Clinical Data Analytics, Biostatistics, Medical Writing, or related domains


• Strong experience in scientific/study report writing and clinical data interpretation


• Proven experience in leading and managing data/reporting teams


• Strong understanding of clinical research processes and study data handling


• Experience with statistical interpretation and analytical methodologies


• Proficiency in Excel, SQL, and data analytics/reporting tools


• Exposure to R, Power BI, Tableau, or Python will be an added advantage


• Excellent written and verbal communication skills


• Strong stakeholder management and project coordination abilities

Key Competencies

• Scientific & Analytical Thinking


• Leadership & Team Management


• Statistical Interpretation


• Attention to Detail


• Report Writing & Documentation Excellence


• Problem Solving & Decision Making


• Stakeholder Management


• Project & Time Management

Preferred Qualifications

• Experience in Clinical Research, CRO, Healthcare Analytics, or Scientific Reporting environments


• Exposure to eCRF/study data handling and clinical databases


• Understanding of regulatory and compliance requirements in clinical research


• Prior experience managing sponsor-facing reporting deliverables