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For your reference, we have included the original job posting below.
Associate Director, Clinical Data Management
Job Number:
26491715
Company Name:
Covance
Job Location:
Princeton, NJ US
Job Category:
Healthcare & Medical
Associate Director, Clinical Data Management
Business Title Associate Director, Clinical Data Management Requisition ID 22673BR Job Category Clinical Research Locations USA - Princeton, NJ Shift 1 Job Posting Imagine working in one of the most exciting and professionally satisfying industries anywhere. Imagine being involved in cutting-edge projects on a daily basis. At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world's largest and most respected contract research organizations. Our clients are a Who's Who of the pharmaceutical and biotechnology industry. If you're looking for a diverse and stimulating work environment, you'll find it at Covance.
TheAssociate Director, Clinical Data Managementis responsible for delivering data management services to clients and project teams, management of staff and contractors, and maintenance of optimal department processes while implementing excellent project-specific strategies.
Responsibilities: . Develop and maintain close positive relationships with counterparts within client organizations: Project Managers, core project team members and others to drive collaboration, consistent expectations, proactive management of risks, productive interdepartmental communications and excellent project delivery . Provide leadership and supervision of data management study/project leaders as well as junior staff, ensuring effective implementation of project and individual goals, development strategies, mentoring, performance management, recruitment and retention strategies, communication strategies, and serving as a role model for Covance Values and the professionalism of Data Management . Serve as the Global Covance CDM liaison to one or more strategic clients and/or lead strategic departmental global initiatives of high complexity requiring excellent team leadership, strong project/people/budget management skills, and expertise across the full range of CDM processes and drug development generally . Assist with the identification of opportunities to improve productivity and quality, while decreasing cycle times and costs to increase financial margins and market share.
Travel: Approximately 10-15% Domestic and/or International travel required. Education/Qualifications . University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) . Must have broad knowledge of drug development process with particular expertise in clinical trial data handling practices and relevant regulations . Understanding of clinical development budgets and relationship to productivity targets . Thorough knowledge of effective data management practices . Expertise in resource management within a CRO setting . Thorough knowledge of time and cost estimate development and CRO service pricing strategies . Thorough knowledge of ICH Guidelines and GCP including regional regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing . Fluent in English, both written and verbal Experience . Minimum seven (7) years of relevant work experience with four (4) or more years supervisory experience to include data management, clinical operations, biostatistics or related field and knowledge of several therapeutic areas. . Demonstrated skill for management of staff exceeding 10 employees across one or more locations within a region (Europe, North America, Asia-Pacific, etc.) . Excellent oral and written communication and presentation skills . In depth knowledge of clinical trial process and data management, clinical operations, biometrics, and systems applications to support operations . Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies . Operational experience in other disciplines such as clinical, biometrics, medical writing, pharmacovigilance, safety, quality assurance, regulatory, etc. . Demonstrates ability to lead change by example and achieve results . Demonstrated ability to handle multiple competing priorities simultaneously across an assortment of projects and initiatives . Demonstrated ability to inspire effective teamwork and motivate staff . Proven managerial and interpersonal skills
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.
Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.
