IQVIA Biotech is hiring Clinical Data Management professionals
IQVIA Biotech is hiring Clinical Data Management professionals.
Skills End to End CDM activities.
Work Location – Thane/Bangalore
Walk-in Drive – Thane Location
Date & Time : 19th Nov’22 – 10 AM to 1 PM
Clin Data Coordinator
Job Overview : Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes DE), or serve in a leadership role to a specific DM Task.
Essential Functions
- Manage delivery of projects through full data management study life-cycle (with minimal guidance).
- With guidance from DTL or Manager, manage project timelines and quality.
- Determine resource needs.
- Identify out-of-scope work.
- Serve as Data Operations Coordinator or Data Team Lead (with guidance).
- Perform comprehensive data management tasks including data review, writing and resolving data clarifications.
- Perform database designer activities for technologies not requiring extensive programming.
- Perform comprehensive quality control procedures.
- Independently bring project solutions to the CDM team.
- Solve issues through using the global issue escalation/communication plan.
- Consult with Standards Group for process issues.
- 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 team.
- Interact with CDM team members to negotiate timelines and responsibilities.
Qualifications
- Bachelor’s Degree Health, clinical, biological sciences, or related field Req
- 1 year clinical trials experience in function similar to DM; or equivalent combination of education, training and experience Req
- Good understanding of clinical drug development process. Intermediate
- Background in medical terminology, Pharmacology, Anatomy, and Physiology. Intermediate
- Excellent organizational, communication, and data management skills (detailed oriented). Intermediate
- Ability to establish and maintain effective working relationships with coworkers, managers and clients. Intermediate
Assoc Clinical Data Manager
Assoc Clinical Data Manager
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 megatrial, 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.
- Manage CDM customer relationship 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 back-up for Data Operations Coordinator or Data Team Lead
- Provide leadership to Operations team
- Provide specific CDM task or technology expertise. Manage 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 customer. 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 through using the global issue escalation/communication plan. Consult with Standards Group for process issues
- 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.”
Qualifications
- 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.
- Thorough knowledge of the data management process
- Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
- Previous experience and proven competence in managing delivery of project through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III). Comprehensive understanding of 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 delivery of project through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III).
- Comprehensive understanding of 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
Experience – 2.5 to 8 years in CDM
