Assistant Manager, Clinical Data Management

## 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 team
- May also perform Lead Data Manager role; oversee/ drive the DM deliverables for the project, communications with the stakeholders, ensuring adherence to timelines
- Utilize therapeutic knowledge and possess a deep understanding of the technology used to review data to ensure database deliverables are consistent and accurate
- Overall responsible for resource allocation and delivery of studies on time with quality
- Build up the system, process & standards for Clinical Data Management activities
- Develop SOPs, work-instructions, work-flow as per regulatory requirements & global standards using good Clinical Data Management practices
- Perform quality checks on the activities performed by peers
- Review study documentation archival
- Analyze & maintain quality trackers; provide status and metrics details to Senior Clinical Data Management on regular basis
- Hiring, training and mentoring of new or existing team members in the CDM unit
- Proactive participation in appropriate project/ functional/ organizational meetings and initiatives
- Participates in the review of cross-functional procedures
- Continuous improvement of functional processes and procedures to ensure DM is consistently maximizing efficiencies
- May indirectly supervise the work of junior members of the project team
- Participation in reviewing and responding to or sponsor audits/ inspection reports
- To carry out other responsibilities as and when required or assigned by the management.

## Your Qualifications and Experience

- Master's degree in Lifesciences, Pharmaceutical Sciences, Biotechnology or related discipline.
- Minimum 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.