Clinical Data Specialist/Assoc Clin Data Coordinator

IQVIA; Bengaluru; On-site; INR 600,000 - 1,200,000; Full time

Job summary

IQVIA Bangalore-based Clinical Data Specialist role seeks candidates with 1–6 years in CDM. You will provide data management support for one protocol, conduct data reviews, and help with database testing and specifications under leadership guidance.

Responsibilities include potential back-up DOC/DTL, data clarifications, and coordinating with the CDM team to ensure quality deliverables for customer needs.

Qualifications

• Bachelor's degree in clinical/biological/mathematical sciences or related field.
• Experience in clinical data management and data handling.

Responsibilities

• Serve as Data Operations Coordinator for a protocol with small to medium-sized teams.
• Perform data reviews, data clarifications, and database testing as needed.
• Lead database design tasks and support programming tests.
• May act as back-up DOC or DTL and coordinate with CDM team.

Skills

Startup

Conduct

Closeout

Medidata RAVE

VEEVA

Education

Bachelor's Degree in Clinical, biological or mathematical sciences

Tools

Medidata RAVE

VEEVA

Job description

## Clinical Data Specialist/Assoc Clin Data CoordinatorApply: Bangalore, India: Full time: Posted Today: End Date: October 18, 2026 (1 day left to apply): R1573836Job Overview Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.**Experience - 1-6yrs** ( Core Data Management)**Location - Bangalore, Thane,Pune, Kolkata, Kochi , Hyderabad****Must have skills - Startup , Conduct , Closeout and Medidata RAVE/RAVE, VEEVA**Essential Functions • Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance. • May serve in the role of back-up to a DOC or DTL. • May conduct data review. • May write and resolve data clarifications. • May lead database audit team. • May develop and test databases and edit specifications. • May perform testing of programming. • May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team.\"Qualifications • Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req • Equivalent combination of education, training and experience in lieu of degree. • Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.