Work as Centralized Data Management Lead at Pfizer
Post : Centralized Data Management Lead India (Team II)
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Job Description
• Regionally focused data management oversight & workload management.
• Manage data associates and interface with functionally responsible roles.
• Ensure escalations, business process & solution achieves business needs.
• Contribute to evolving data management & serve as a change agents with regional contact.
• Liaise with regional BU strategists, and any other applicable partner lines at local (clinical, safety and medical area among others)
• Coordinate the issuing of the reports and metrics as per need to evaluate team performance and data entry compliance.
• Perform quality control of timeliness and accuracy data.
• Develop key performance indicators in order to ensure accurate and timely execution of improvement initiatives and guarantee increased compliance in relevant processes.
• Propose process enhancements as per BAU learnings.
• Ensure team receives appropriate training materials and its correct implementation.
• Coordinate with remote/local peers to ensure compliance with local and global regulatory requirements.
• Develop and propose strategies to improve efficiencies and effectiveness while managing the data management activities.
• Responsible for develop and enhance the capabilities and capacities of the SCC team throughout the identification and implementation of training and development needs.
• Adhere to the appropriate use of technical tools, through use of working practices and qc/qa procedures such as regulatory and internal compliance.
• Responsible for cluster teams professional development through coaching and motivation
• Coach, mentor and develop staff, including overseeing new employee onboarding and providing career development planning and opportunities
• Lead cluster data associate team using the performance management framework and development process that provides an overall context and framework to encourage employee contribution; includes goal setting, feedback, and performance development planning
• Lead cluster data associate team to meet the organization’s expectation’s for productivity, quality and goal accomplishment
• Impact on the organization:
• Efficient use of resources through operational effectiveness.
• Improved accuracy and quality of global regulatory systems updates.
• Reduce the CRL workload in terms of the updating data in Global Regulatory Systems.
Candidate Profile
• Demonstrated experience in managing teams and people
• Regulatory experience in regulatory activities
• Master or undergraduate degree plus relevant experience in life science or business
• Minimum of 5 years of relevant experience
• Multi-lingual skills desirable
• Project Leadership
• Demonstration of experience working in a challenging customer service environment
• Communication Skills: ability to communicate complex information and analyses to a variety of audiences in both verbal and written format.
• Project Management skills: Mastery of processes, tools and techniques for planning and monitoring projects to established deadlines. Familiarity with pharmaceutical organizational structures, systems, and culture.
• Demonstrable experience across the Drug, Discovery, Development and commercialization lifecycle, with proven examples of contribution.
• a variety of audiences in both verbal and written format.
• Project Management skills: Mastery of processes, tools and techniques for planning and monitoring projects to established deadlines. Familiarity with pharmaceutical organizational structures, systems, and culture.
• Demonstrable experience across the Drug, Discovery, Development and commercialization lifecycle, with proven examples of contribution.
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Technical Skill Requirements
• Understanding of the concepts around regulatory activities.
• Understanding of regional regulatory requirements.
• Articulate with analytical and interpersonal skills.
• Proven aptitude in project management and process redesign.
• Demonstrated coordination of activities in a highly regulated environment.
• Knowledge of the local regulatory environment and how this impacts regulatory strategy and implementation.
• Knowledge of drug development practice, rules, regulations and guidelines.
• Communication skills.
• Negotiation skills.
• Analysis and problem solving skills.
• Understanding stakeholder needs.
• Customer service orientation.
• Network and alliance building/ peer relationships.
• Influencing skills.
• Successful experiences of teamwork, seeking and proposing alternative solutions, achieving goals in an inclusive manner.
• Interpersonal acumen.
• Organizational agility.
• Strong quality and compliance orientation.
• Detailed oriented.
• Analytical Thinking.
• Adaptability.
• English intermediate to advance (written and spoken)
• Fluent in other languages dependant on cluster
Additional Information:
Experience: 5 years
Location: Chennai
Education: Master in life science or business
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area: Centralized Data Management
Job ID: 4686199
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