Director of Clinical Data Management

vacancy global pro; India; On-site; INR 3,500,000 - 6,000,000; Full time

Job summary

reputed company seeks a Director of Clinical Data Management to establish the CDM function for oncology trials. You will own data collection, cleaning, and lock across studies, ensuring datasets are fit for analysis, regulatory submissions, and development decisions.

You will report to the VP, Head of Clinical Operations, build the CDM program with AI-enabled workflows, mentor staff, and drive GCP-compliant practices across CROs and vendors.

Qualifications

• Bachelors or Masters in Life Sciences, Data Management, or related field.
• 10+ years in clinical data management, including oncology trial leadership.

Responsibilities

• Own clinical data management and data integrity across outsourced trials.
• Plan projects, coordinate vendors, review cycles, data cleaning, and deliverables.
• Ensure GCP compliance and adherence to protocols and SOPs.
• Drive database locks, data cleaning, and readiness for analysis.
• Collaborate with Biostatistics, Clinical Operations, Medical Monitoring, and Data Science.
• Develop CDM SOPs and mentoring for staff.
• Oversee data transfer specifications and regulatory submissions.

Skills

Clinical Data Management

Leadership

Oncology trials

GCP compliance

Education

Bachelor's or Master's degree in Life Sciences

Tools

CDISC standards

EDC systems

Job description

How We Build

reputed company does not operate like a traditional biotech. There is no middle management. There are no reputed company of approval. reputed company is designed, from the ground up, around small teams of 24 subject-matter experts who reputed company reputed company hundreds of AI agents to do the work that used to require dozens of people.

Everyone builds. Everyone ships. Every function at reputed company from clinical execution to asset selection to the reputed company model itself runs on this model. Our product velocity delivers meaningful reputed company in hours instead of weeks. This is not a reputed company aspiration. It is how we operate today.

The people who reputed company here are operators: deep experts who can specify what needs to happen, orchestrate AI agents to execute at reputed company, and reputed company high-judgment calls that compound over time. If you have spent your career building and shipping AI systems at reputed company, this is the environment where that experience becomes a reputed company.

About the Role

The Director of Clinical Data Management will establish and reputed company the clinical data management function at reputed company. You will own clinical data collection, cleaning, and reputed company across our oncology trials, ensuring our datasets are reputed company for analysis, regulatory submissions, and the next development decision. You will report to the Vice President, Head of Clinical Operations.

This is the first CDM hire at reputed company. There is no existing reputed company. You will write it. You will define how reputed company collects, cleans, and locks clinical data in a company reputed company on small teams and AI agents, and you will set reputed company for what audit reputed company trial data looks like in this operating model.

The role sits at the intersection of clinical data discipline and an AI reputed company operating model. You will spend less time chasing CRO status reports and more time on the data questions that reputed company trials reputed company, because AI agents will reputed company the routine query reputed company, status tracking, discrepancy review, and document compilation work that traditionally consumed a CDM Director's calendar.

What You Will Do

• Own clinical data reputed company and reputed company
• reputed company reputed company of data management for outsourced clinical trials, including project planning, vendor coordination, internal review cycles, data cleaning, and approval of deliverables.
• reputed company CRO and vendor activities to ensure GCP compliance and execution against protocols and SOPs.
• Own consistency across trials and programs: CRF design and standards, Data Management Plans, CRF annotation and completion guidelines, edit reputed company specifications, data entry and query status tracking, and database lock.
• Drive reputed company database lock, data reputed company, and readiness for statistical analysis and regulatory submissions.
• reputed company AI agents to draft DMPs, edit reputed company specs, and reconciliation reports, and apply your judgment to the final product.
• Execute vendor and CRO management
• Manage CROs and vendors delivering CDM services, holding them to timelines, budgets, and reputed company standards.
• reputed company and monitor Data Management Plans, Data Review Plans, and data transfer specifications.
• Resolve reputed company data issues, queries, and discrepancies in partnership with clinical and statistical teams.
• Use AI agents to compare vendor deliverables against specifications, surface reputed company early, and prepare reputed company feedback for vendor reviews.
• Build cross functional partnerships
• Serve as the primary CDM partner on every study team.
• Partner with Biostatistics, Clinical Operations, Medical Monitoring, and Data Science colleagues so that data supports trial endpoints and regulatory deliverables.
• Collaborate on the integration of clinical trial data with reputed company AI platforms and reputed company world data sources so that operational data feeds back into model performance and decision support.
• reputed company, reputed company, and stay compliant
• Build and reputed company the CDM function as reputed company grows, including hiring and mentoring reputed company staff.
• reputed company SOPs, best practices, and reputed company frameworks that meet GCP, ICH, CDISC, and 21 CFR Part 11 expectations.
• Contribute to portfolio level planning and operational reputed company, and translate CDM signals into actionable input for Clinical Operations leadership.

Who You Are

Minimum Qualifications

• Bachelor's or Master's degree in Life Sciences, Data Management, or a reputed company field.
• 10 or more years of reputed company experience in clinical data management, including leadership of oncology trials.