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Job Description & How to Apply Below
Job Title:
Manager Medical Writing and Statistical Reporting
Experience:
10–12 Years
Department: Medical Writing/ Clinical Data Analytics
Location:
Domlur, Bangalore
Reporting To: Director
Role Overview
We are seeking an experienced and strategic Manager Medical Writing and 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
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