Clinical Data Specalist / Senior clinical Data Coordinator

IQVIA Inc; Ernakulam; Sur place; INR 600 000 - 900 000; Plein temps

Résumé du poste

IQVIA Inc in Kochi, India seeks a Clinical Data Specialist / Senior Clinical Data Coordinator to provide data management support within the CDM team. You will help ensure data quality, lead small tasks, and collaborate with study teams to resolve data queries.

The role requires a degree in clinical/biological sciences, strong attention to detail and communication. It is a full-time on-site position with exposure to multiple protocols under supervision.

Qualifications

• Bachelor's degree in clinical, biological or mathematical sciences or related field.
• Equivalent combination of education, training and experience in lieu of degree.
• Medical terminology exposure. Excellent organizational, communication and leadership skills.

Responsabilités

• Serve as a Data Operations Coordinator (DOC) for one protocol with small ops staff or lead a data management task with guidance.
• May conduct data review and write/resolve data clarifications.
• May lead database audit team and develop/test databases.

Connaissances

Data management

Medical terminology

Attention to detail

Communication

Formation

Bachelor's degree in Clinical/biological or mathematical sciences

Outils

Database design

Testing databases

Description du poste

Clinical Data Specalist / Senior clinical Data Coordinator### Clinical Data Specalist / Senior clinical Data CoordinatorApply: Kochi, India: Full time: Posted Today: End Date: December 1, 2026 (30+ days left to apply): R1569000Job 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.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.