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Assoc Dir, Clinical Data Acquisition and Mgmt

Novartis
Remote friendly (East Hanover, NJ)
United States
$138,000 - $257,000 USD yearly
Operations

Role Summary

Assoc Dir, Clinical Data Acquisition and Management leads a team of ~20 Clinical Data Acquisition Specialists, Clinical Data Scientists and Coding Specialists. Responsible for staffing/resource allocation, people management, career development and engagement across the CDAM community, and for facilitating resource sharing between groups to meet portfolio goals. Location: East Hanover, NJ.

Responsibilities

  • Recruit, manage and develop team of Clinical Data Acquisition and Management (CDAM) associates/roles to ensure high-performance
  • Facilitate a customer-oriented Clinical Data Acquisition and Management group, role modeling behaviors per company Values and Behaviors
  • Accountable for assignment of resources and workload and ensuring resource sharing between groups to meet objectives and priorities
  • Partner with functional mentors and Functional Experts within CDAM to empower associates to resolve issues at the trial/program delivery level
  • Participate in Health Authority inspections as required
  • Build and foster a strong team spirit founded on technical ability and performance
  • Lead/support non-clinical special projects and initiatives, providing subject matter expertise as needed
  • Identify training needs and support the establishment and documentation of training for CDAM associates, ensuring training compliance
  • Ensure high-quality communication and information flow on trial status to stakeholders, and mitigate/manage risks

Qualifications

  • Required: Bachelorโ€™s degree in life science, computer science, pharmacy, nursing or equivalent relevant degree
  • Required: 10 yearsโ€™ experience in Drug Development with at least 6 years in Clinical Data Management
  • Required: 4 years line management or leadership experience
  • Required: Proven leadership, collaboration and organizational skills with ability to manage simultaneous trials and meet deadlines
  • Required: Excellent understanding of clinical trials methodology, GCP and medical terminology
  • Required: Ability to anticipate challenges and risks and proactively suggest/implement solutions
  • Required: Ability to work under pressure with agile, innovative team leadership
  • Required: Excellent interpersonal skills and ability to operate effectively in a global environment
  • Required: Ability to influence and communicate across functions and external stakeholders

Preferred

  • Prior experience in Pharma