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Clinical Data Manager
Location – Lawrence NL
Duration – 10 Months
Direct Client BMS
50% Onsite 50% remote

Position Responsibilities
• Support and contribute to the development, embedding, growth and health of the necessary
business process to support risk mitigation and global monitoring processes that align with
the risks of BMS programs and protocols.
• Support execution of RBM processes as a part of cross-functional teams spanning the R&D
portfolio (all therapeutic areas and phases of development).
• Utilize analytics/visualizations to review aggregate data for the remote assessment of Risk
Indicators that identify issues and emerging risks at the study, program, country, therapeutic
and functional level, to ensure risks are addressed consistently.
• Identify critical data issues and document findings for tracking and timely resolution.
• Contribute to the development of or provide feedback on documented processes developed for risk-based monitoring methodology being adopted by BMS.
• Contribute to the development of or provide feedback on training material developed to
support RBM methods.
• Accountable for supporting global inspection readiness and inspections in regard to RBM
monitoring process and tactics
• Provide user input on IT needs necessary to support all aspects of RBM.
• Contribute to the development and maintenance of metrics that inform the evaluation of
central monitoring performance and effectiveness.
• Acts as a change agent with stakeholders across R&D, including educating, bridging
• knowledge across functions and developing effective partnerships with critical stakeholders.

Degree Requirements
• 4 Year Degree required in one of the following disciplines or related field: Life Sciences; Analytics; Data Science; Statistics; Business Experience Requirements
• 3+ Years in drug development is preferred
• 3+ Years in the field of site management, site monitoring, data management or related is preferred

Key Competencies
• Demonstrated ability to effectively communicate ideas/concepts and to motivate others to
• accomplish challenging shared goals and objectives.
• Well-versed in analytical and conceptual capabilities
• Demonstrated ability to apply critical thinking and identify, distinguish relative importance and
• be able to work through issues remotely
• Demonstrated knowledge of clinical operations, inclusive of site monitoring, management
and data management
• Demonstrated knowledge of Good Clinical Practices (GCP)
• Demonstrated ability to absorb critical knowledge on relevant protocol/trial design
• requirements as well as relevant clinical/disease area knowledge
• Demonstrated ability to successfully manage competing priorities to achieve the goals of the
• department and the larger organization.
• Thorough knowledge of global regulatory and guideline (inclusive of ICH GCP) requirements
• with clinical experiences in a drug development capacity
• Demonstrated ability to build and maintain strong relationships across organizational and/or
• geographic boundaries through participation on cross-functional teams

Interested candidates please send your resume at antim.jain@fortira.com or call me at +1-609-454-0507 for Immediate consideration.

Reference : Clinical Data Manager - W2 Only jobs

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Published at 17-04-2023
Viewed: 123 times