Senior Clinical Data Manager – Remote | Full-Time | Bangalore
Location: Bangalore (Remote)
Job Type: Full-Time
Department: Clinical Data Management / Biometrics
Experience Required: Minimum 8+ years in Clinical Data Management (including sponsor management and mentoring experience)
Job Overview
We are seeking an experienced Senior Clinical Data Manager to lead end-to-end data management activities across complex clinical trials. This role is responsible for delivering high-quality clinical data from study start-up through database lock, ensuring compliance with global regulatory standards, sponsor expectations, and project timelines.
The ideal candidate brings deep expertise in clinical trial data management, strong sponsor-facing experience, leadership capability, and a proven ability to manage budgets, scope, and cross-functional teams within a CRO or pharmaceutical environment.
This position is remote-based in Bangalore with occasional travel requirements.
Key Responsibilities
Study Leadership & Accountability
Lead data management activities for clinical studies involving healthy volunteer and patient populations, multi-site trials, complex protocol designs, and accelerated timelines.
Take full accountability for all assigned Data Management deliverables within established timelines and budgets.
Oversee study documentation, database setup, data entry processes, validation procedures, and database lock activities.
Ensure adherence to study protocols, global SOPs, ICH-GCP guidelines, and regulatory requirements.
Sponsor & Stakeholder Management
Act as Subject Matter Expert for Data Management in sponsor relationship meetings.
Collaborate directly with sponsors to understand requirements and drive implementation.
Represent Data Management in bid defense meetings and new business opportunities.
Manage scope changes, budget discussions, and customer negotiations in collaboration with Project Managers or FSP Leads.
Address audit findings and sponsor comments within defined timelines.
Cross-Functional Coordination
Partner with EDC Design, SAS Programming, Statistics, PK, Clinical Operations, and other Biometrics teams to align deliverables and ensure timely database lock.
Lead internal data-focused project meetings and proactively identify risks with mitigation strategies.
Monitor deliverables across Biometrics to assess resource and timeline impacts.
Quality & Compliance
Ensure service quality aligns with Data Management Plans and scope of work agreements.
Conduct reconciliation of clinical databases with safety, laboratory, and third-party vendor data.
Maintain accurate documentation and ensure appropriate close-out procedures.
Contribute to SOP development, review, and process improvements.
Team Leadership & Mentorship
Provide leadership, mentorship, and coaching to Data Management teams.
Support performance evaluations and career development initiatives.
Guide junior team members on data management processes and technical capabilities.
Promote adoption of new technologies and industry best practices.
Required Qualifications
Bachelor’s degree or equivalent combination of education and relevant experience.
Fluency in English (spoken and written).
Experience Requirements
Minimum 8 years of combined early- or late-phase Clinical Data Management experience.
At least 2 years of direct sponsor management experience.
Minimum 2 years of technical mentoring or team leadership experience.
Proven experience managing Scope of Work, budgets, and contract negotiations.
Strong knowledge of clinical trial processes, data management systems, biometrics workflows, and regulatory standards.
Experience representing Data Management in bid defense meetings.
Four or more years of Electronic Data Capture system experience preferred.
Preferred Qualifications
Degree in Life Sciences, Health Sciences, Information Technology, or related field.
Strong understanding of CRO operational models and regulatory obligations within the pharmaceutical and biotechnology industries.
Experience working within structured SOP-driven global organizations.
Work Environment & Travel
Remote or office-based role.
Potential travel up to 10%, including occasional overnight stays.
Extended computer usage may be required.
Apply Now
If you are an experienced Clinical Data Management professional seeking a leadership opportunity in a global clinical research environment, apply now to advance your career and contribute to high-impact clinical trials.
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