Assistant Manager, Clinical Data Management

Teva Pharmaceuticals · Bengaluru

  • Experience8–10 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Levelexecutive
  • Posted21 Sept 2026

About Teva Pharmaceuticals

Teva Pharmaceuticals is hiring in Bengaluru in pharma biotech. This role looks for around 8+ years of experience.

Skills

  • Clinical Data Management
  • therapeutic knowledge
  • regulatory requirements
  • clinical data systems
  • Standard Operating Procedures
  • good Clinical Data Management practices
  • quality checks
  • resource allocation
  • study documentation archival
  • quality tracking
  • Clinical Data Management experience

The role

A clinical data manager at a biopharmaceutical company oversees Clinical Data Management studies, applies therapeutic knowledge and regulatory requirements, and builds clinical data systems and standards. The role also performs quality checks and develops Standard Operating Procedures.

Full job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

How You’ll Spend Your Day

Perform Subject Matter Expert role; providing knowledge and expertise; helping to resolve issues and challenges faced by the teamMay also perform Lead Data Manager role; oversee/ drive the DM deliverables for the project, communications with the stakeholders, ensuring adherence to timelinesUtilize therapeutic knowledge and possess a deep understanding of the technology used to review data to ensure database deliverables are consistent and accurateOverall responsible for resource allocation and delivery of studies on time with qualityBuild up the system, process & standards for Clinical Data Management activitiesDevelop SOPs, work-instructions, work-flow as per regulatory requirements & global standards using good Clinical Data Management practicesPerform quality checks on the activities performed by peersReview study documentation archivalAnalyze & maintain quality trackers; provide status and metrics details to Senior Clinical Data Management on regular basisHiring, training and mentoring of new or existing team members in the CDM unitProactive participation in appropriate project/ functional/ organizational meetings and initiativesParticipates in the review of cross-functional proceduresContinuous improvement of functional processes and procedures to ensure DM is consistently maximizing efficienciesMay indirectly supervise the work of junior members of the project teamParticipation in reviewing and responding to or sponsor audits/ inspection reportsTo carry out other responsibilities as and when required or assigned by the management.

Your Qualification And Experience

Master's degree in Lifesciences, Pharmaceutical Sciences, Biotechnology or related discipline.8-10 years of relevant Clinical Data Management experience.CCDM would be considered an added advantage

How We’ll Take Care Of You

At Teva India, care is at the heart of how we work. From your first day, you’ll be welcomed into a people-first culture built on inclusion, respect, and belonging.

That support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You’ll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.

Your growth matters too. You’ll have opportunities to build future-ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI-enabled Teva Twist program, R&D Academy, continuing education, and mentorship.

Join our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.