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Data Manager

Trenton, NJ 08648

Posted: 01/31/2023 Employment Type: Contract Job Category: Data Sciences Job Number: 537675 Is job remote?: No Country: United States

Job Description


This person will be part of the Centralized Monitoring group working as a Central Monitor within GDMCM. Job Description has the details for the Central Monitor role. The role is required to be in the office 50% over 2 weeks as per Client  Flexible Ways of Working.

The Contract Central Monitor will perform Central Monitoring activities. The Central Monitor (CMN) plays a critical role contributing to the development, embedding, growth and health of the central monitoring capability in support of Risk Based Monitoring (RBM) methodology adopted by Client.

The CMN is responsible for the remote assessment of Risk Indicators that identify issues and emerging risks in study-specific variables (trends / outliers / poor performing sites) through the review of aggregate data. Central monitors are responsible for the review of clinical and operational data.

The CMN will interact with clinical teams and regionally based Site Monitors/Managers to support the oversight of the sites/studies as per the Risk Based Monitoring methodology adopted by Client.

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 Client programs and protocols. l Support execution of RBM processes as a part of cross-functional teams spanning the R&D portfolio (all therapeutic areas and phases of development). l 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 Client.
  • Contribute to the development of or provide feedback on training material developed to support RBM methods. l 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 l 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 l 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.

Skills:
SPOTFIRE

37-42 pay rate range
**salary will be commensurate with experience**
 

The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.

Planet Pharma and The Planet Group of Companies are equal opportunity employers. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.

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Although this hasn't been an issue at The Planet Group, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at The Planet Group.

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