clinical data management job openings in iqvia India
clinical data management job openings in iqvia India
Location – Thane/ Bangalore/ Kochi
No fresher and CRC
Minimum 3+ Years in Clinical Data Management
Job Overview
Provide comprehensive data management expertise to Clinical Data Management (CDM) to provide efficient, quality data management products that meet customer needs. Provide leadership either in the role of the Data Operations Coordinator (DOC), the role of the Data Team Lead (DTL), or in a leadership role in a specific CDM task (e.g., lead of a task on a mega trial, coder, tester, database designer for technologies that don’t require extensive programming expertise).
Essential Functions
- Serve as Data Team Lead (DTL) on multiple global clinical trials or 35+ increasingly complex central laboratory studies.
- Provide leadership to CDM team.
- Managed CDM customer relationships for CDM project team including active participation in DM customer negotiation on timeline, budgetary and other issues (with guidance).
- Provide marketing capabilities presentations and business development presentations. . Or serve as Data Operations Coordinator (DOC) for one or two global clinical trials with fewer than 20 operations staff (excludes DE) or 20-30 central laboratory studies, or serve in a leadership role to a specific data management task.
With minimal guidance, serve as backup for Data Operations Coordinator or Data Team Lead - Provide leadership to the Operations team
- Provide specific CDM tasks or technology expertise. Manage the delivery of projects through full data management process life-cycle. With minimal guidance, manage project timelines and quality issues, determine resource needs, and identify and justify out-of-scope.
- Provide input for negotiations with customers. Provide comprehensive data management expertise (including all operations tasks and creation of project specifications).
- Perform comprehensive quality control procedures. Independently bring project solutions to the CDM team. Solves issues by using the global issue escalation/communication plan. Consult with the Standards Group for process issues and communicate ideas for process improvement.
- Assist in developing and implementing new technology. Understand and comply with core operating procedures and working instructions.
- Meet objectives as assigned.
- Develop and maintain good communications and working relationships with CDM and project teams.
- Interact with CDM team members to negotiate timelines and responsibilities.”
Qualification
- Bachelor’s Degree Clinical, biological or mathematical sciences, or related field, or nursing qualification Req
- 3 years of related experience including clinical trials experience in a function similar to data management. Equivalent combination of education, training and experience.
- Thorogh knowledge of the data management process. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
- Previous experience and proven competence in managing the delivery of projects through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III).
- Comprehensive understanding of the clinical drug development process. Excellent organizational, communication, and data management skills (detail-oriented).
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Thorough knowledge of the data management process.
- Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
- Previous experience and proven competence in managing the delivery of projects through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III).
- Comprehensive understanding of the clinical drug development process. Excellent organizational, communication, and data management skills (detail-oriented). Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
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