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successfactors

Data Management Associate II (70157)

Teva
IND
Full-time
Senior · 5+ years experience
Onsite
Discovered 1 months ago
Pinnacle 21

Full Job Posting

How You’ll Spend Your Day

Perform Lead Data Manager role; oversee/ drive the DM deliverables for the project, communications with the stakeholders, ensuring adherence to timelines

Proactively coordinate and perform start-up, maintenance and close out activities, as detailed in our SOPs and guidelines

Lead study setup including but not limited to;

Review of the study protocol

Preparation and review of eCRF specifications, Time and Event Schedule, ECS, eCRF Completion Guidelines, DMP, Safety Reconciliation Plan, Manual Listings, UAT Summary, Change Log documents

Create and review of the test scripts for the UAT

Performing UAT for the study

Performing query management which include, query generation and query resolution

Perform SAE reconciliation and Lab/Vendor data reconciliation

Performing manual review of data, Pinnacle 21 and smart listings

Locking the database as detailed in SOP as per timelines for the statistical review

Performing post production changes and assessment of impact on database in consultation with the Database Programmer

Generating metric reports / status reports for the CDM status of the study and informing of any study related issues to relevant stakeholders when required for further action

Maintain study specific documentation as per in-house standards, procedures & regulatory requirements

Participation in reviewing and responding to or sponsor audits/ inspection reports

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

Provide training to site personnel in person or via electronic meetings

Training and Mentoring of team members in accordance with established functional procedures

To carry out other responsibilities as and when assigned by the management.

Your Qualification and Experience

  • Master's degree in Lifesciences, Pharmaceutical Sciences, Biotechnology or related discipline.
  • Minimum 5-7 years of relevant Clinical Data Management experience.

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.

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