PHARMAFull-time
Assistant Manager, Clinical Data Management
BANGALORE (IN)ONSITEPOSTED: 9/26/2026
PHARMAFull-time
HIRING ORGANIZATIONTEVA PHARMACEUTICALSBiopharmaceuticals / Life Sciences
ROLE OVERVIEW
Assistant Manager responsible for leading and supporting Clinical Data Management activities, ensuring accurate and timely study delivery, quality compliance, process improvement and effective stakeholder coordination.
ROLE DEFINITION & RESPONSIBILITIES
- •Serve as a Clinical Data Management subject matter expert and resolve team issues
- •Lead or oversee project data-management deliverables and stakeholder communications
- •Ensure clinical database deliverables are accurate, consistent and compliant
- •Manage resource allocation and timely, quality study delivery
- •Develop systems, processes, SOPs, work instructions and workflows aligned with regulatory requirements and global CDM standards
- •Perform peer quality checks and review study-document archival
- •Maintain quality trackers, metrics and status reporting
- •Hire, train and mentor CDM team members
- •Participate in cross-functional meetings and procedure reviews
- •Drive continuous improvement of CDM processes and efficiency
- •Provide indirect supervision to junior project members
- •Participate in sponsor audits and inspection-response activities
Reporting Hierarchy: Reports to Senior Clinical Data Management leadership; collaborates with project stakeholders, cross-functional teams, sponsors and junior CDM team members
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's or Master's degree in Life Sciences, Pharmaceutical Sciences, Biotechnology or related discipline
- Minimum 10 years of relevant Clinical Data Management experience
- Strong knowledge of Clinical Data Management processes and standards
- Ability to manage study deliverables, timelines, quality and stakeholders
- Ability to develop and implement CDM processes and documentation
PREFERRED QUALIFICATIONS
- •Certified Clinical Data Manager (CCDM) certification
- •Therapeutic-area knowledge
- •Experience with clinical data review technologies
- •Experience with audits and inspections
- •People leadership, mentoring and resource management experience
REQUIRED VERIFIED SKILLS
Clinical Data Management
clinical database management
data review
CDM standards
SOP development
work instructions
workflows
quality checks
quality trackers
clinical study delivery
regulatory compliance
audit readiness
inspection support
metrics reporting
resource allocation
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, Optum Employee Assistance Program, healthy meals at work, wellbeing initiatives, volunteering programs, continuing education, mentorship and internal career opportunities
No salary or bonus/equity information is disclosed in the supplied posting. Compensation should therefore be evaluated using the actual Teva offer and relevant India market benchmarks rather than inferred.
ORGANIZATION CONTEXT & CULTURE
Teva Pharmaceuticals is a global biopharmaceutical company with a major generics business and innovative medicines activities, including neuroscience and immunology. Teva operates globally with a focus on improving access to medicines and patient health.
TEAM SIZE: 50,000+ employees
INDUSTRY: Biopharmaceuticals / Life Sciences
Culture: Teva describes a people-first, inclusive and collaborative culture with emphasis on professional growth, global teamwork, wellbeing, learning and continuous improvement.
EXPECTED CAREER ROADMAP
Potential progression includes Senior Clinical Data Management leadership, Clinical Data Management Lead/Manager, Associate Director and broader clinical operations or data-management leadership roles, depending on organizational structure and performance.
APPLICATION ADVISORY
Emphasize 10+ years of CDM experience; demonstrate ownership of study deliverables and timelines; highlight database quality, SOP/workflow development and regulatory compliance; showcase audit/inspection experience; mention CCDM if held; quantify team leadership, mentoring or process-efficiency improvements.
RECOMMENDED TRAINING
1/5
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