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Quintiles is the only fully integrated BioPharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. The Quintiles network of 23,000 engaged professionals in more than 50 countries around the globe works with an unwavering commitment to patients, safety and ethics. Quintiles helps biopharmaceutical companies navigate risk and seize opportunities in an environment where change is constant. For more information, please visit www.quintiles.com. Various compensation and benefits programs are available depending on position, years of experience and geographic location. Many of the benefits of working with Quintiles go beyond financial re-numeration and include job related training, company recreational events, and community support activities.
Quintiles is an Equal Opportunity Employer M/F/D/V.
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Home based Opportunities Available! Statewide!
The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic Assistant Clinical Data Manager/Data Team Lead to join our team! Purpose: Provide comprehensive data management expertise to Data Management to provide efficient, quality data management products that meet customer needs. Provide leadership role as a Data Team Lead (DTL) or in a leadership role in a specific DM task (e.g. lead of a task on a megatrial, coder, database designer for technologies that don’t require extensive programming expertise). Responsibilities:
- Serve as Data Team Lead (DTL) on multiple global studies.
- Provide leadership to DM team.
- Manage DM customer relationship for DM 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.
- Serve as Data Team Lead for one or two global studies with fewer than 20 operations staff
- (excludes DE), or serve in a leadership role to a specific DM Task.
- With minimal guidance, serve as back-up for Data Operations Coordinator or Data Team Lead, providing leadership
- and technical expertise to Operations team.
- 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 DMP generation).
- Perform database designer activities for technologies not requiring extensive programming.
- 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 team.
- Interact with CDM team members to negotiate timelines and responsibilities.
- Bachelor’s degree in clinical, biological or mathematical sciences, nursing degree or related field, with a minimum of 3 years experience in a clinical data management role, specifically in a CRO, pharmaceutical or biotech environment or the equivalent of education, training or experience.
- Candidates must have prior work experience in a lead role, managing assigned projects on all levels, acting as the project lead.
- Candiate must have a thorough knowledge of the clinical trial data management process.
- Knowledge of Medical Terminology, Pharmacology, Anatomy, and 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.

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