PHARMAFull-time
Assistant Manager, Clinical Data Management
By Admin · Clinical Data Management
BANGALORE (IN)ONSITEPOSTED: 10/2/2026
PHARMAFull-time
HIRING ORGANIZATIONTEVA PHARMACEUTICALSBiopharmaceuticals / Life Sciences
ROLE OVERVIEW
Leads and supports Clinical Data Management delivery with subject matter expertise, study oversight, quality control and process improvement. The role combines technical CDM expertise with resource coordination, mentoring, standards development and audit support.
ROLE DEFINITION & RESPONSIBILITIES
- •Serve as a Clinical Data Management subject matter expert and resolve team issues
- •Lead or oversee project data-management deliverables, stakeholder communication and timelines
- •Allocate resources and ensure study delivery meets quality and timelines
- •Build systems, processes and standards for Clinical Data Management activities
- •Develop SOPs, work instructions and workflows aligned with regulatory requirements and global CDM practices
- •Perform quality checks, maintain quality trackers and provide status and metrics reporting
- •Hire, train, mentor and indirectly supervise CDM team members
- •Support sponsor audits, inspection responses, cross-functional procedures and continuous process improvement
Reporting Hierarchy: Reports to Senior Clinical Data Management leadership; Provides subject matter expertise and may indirectly supervise junior project-team members while coordinating with cross-functional stakeholders and sponsors
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's or Master's degree in Lifesciences, Pharmaceutical Sciences, Biotechnology or a related discipline
- Minimum 10 years of relevant Clinical Data Management experience
- Strong knowledge of Clinical Data Management processes and technology
- Experience delivering clinical data management studies with quality and timeline accountability
- Experience supporting regulatory or sponsor audits and inspections
PREFERRED QUALIFICATIONS
- •Certified Clinical Data Manager (CCDM)
- •Experience in developing SOPs, work instructions and CDM standards
- •Experience leading or mentoring Clinical Data Management teams
- •Strong therapeutic and technology knowledge
REQUIRED VERIFIED SKILLS
CCDM
Therapeutic Knowledge
Clinical Technology
Cross-functional Collaboration
People Management
Sponsor Communication
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.
Emphasize 10+ years of Clinical Data Management experience; demonstrate study delivery ownership, resource allocation and quality oversight; highlight SOP and workflow development; show experience with CDM technologies and data review; mention audit and inspection support; highlight mentoring, hiring and team leadership experience; include CCDM certification prominently if held.
ORGANIZATION CONTEXT & CULTURE
Teva Pharmaceuticals is a global biopharmaceutical company with a major generics business and innovative medicines focused on areas including neuroscience and immunology. Its India organization supports global pharmaceutical research, development and operations.
TEAM SIZE: Teva describes a people-first, inclusive and collaborative culture with emphasis on fresh thinking, professional development, wellbeing, global collaboration and continuous learning.
INDUSTRY: Biopharmaceuticals / Life Sciences
Culture: Rolling admissions
EXPECTED CAREER ROADMAP
No salary range or bonus/equity information is disclosed in the provided job posting. Compensation should therefore not be inferred from the role title or experience requirement.
APPLICATION ADVISORY
[https://www.tevatwist.teva/careerhub/explore/jobs/563602813553635
RECOMMENDED TRAINING
1/5
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