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Assoc Dir Global Development Training

Regeneron Pharmaceuticals

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Job Details

Location: Ireland Posted: Sep 26, 2022

Job Description

The Training Business Partner for REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY is responsible for executing the design and delivery of training to REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY associates. The Training Business Partner will collaborate with the REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY stakeholders, Process and Procedures, SMEs and Global Development Training to implement initiatives in line with the GCO strategic objectives. The Training Business Partner is directly responsible for executing training that drives quality and compliance and ensuring the highest level of customer satisfaction within REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY.

JOB DUTIES: List essential (6-10) to be performed. These are the most critical responsibilities

Strategic Alignment:

  • Understand the business and associated roles within REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY and identify key targeted learning and development needs.
  • Partner with REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY to align learning and development tactical plans with REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY strategy.

Relationship Management

  • Serve as primary point of contact for all REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY training related initiatives
  • Establish, deepen and sustain key relationships with REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY stakeholders to understand business needs and related performance gaps, and demonstrate understanding of processes and methodology to provide appropriate learning solutions.

Design Support and Performance Consulting

  • Perform needs assessment and facilitate development of an ongoing plan with a focus on continuous improvement measured through participant feedback, assessment, monitoring of performance and other KPIs
  • Work closely with REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY functions, Learning Center of Excellence, Process and Procedures and SMEs to continually improve the scale, depth and quality of training across REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY.

Curriculum Support

  • Partner with REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY to provide a broad range of training solutions to cover role specific onboarding, continuous learning and REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY project specific initiatives.
  • Ensure that all training is designed and executed consistent with SOPs. Work with Process and Procedures to develop targeted training for REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY and support the design, development and delivery of supplemental training to help REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY associates understand policies, process and procedures in key compliance risk areas

Solution Scoping/Management

  • Ensure effective implementation and on time delivery of learning solutions
  • Source, scope and manage all REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY training initiatives.
  • Create and manage key initiatives focused on driving compliance and performance improvement for REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY partners
  • Collaborate with Training Ops in updating and populating REGULATORY AFFAIRS AND GLOBAL PATIENT SAFETY training assets and information on LMS and associated portal pages.

TEAM MEMBERSHIP AND KEY INTERFACES:

List key team memberships and cross-functional interfaces essential for success in this role

Cross Functional Interfaces

  • Reg Affairs and Global Patient Safety
  • Learning Center of Excellence
  • Process and Procedures

JOB REQUIREMENTS:

List knowledge, skills, and abilities required to perform the job.

List any preferred job requirements as well.

  • At least 8 years of relevant industry experience
  • Minimum of 5 years in a training capacity
  • Minimum of 3 years’ experience in GCP training
  • Background in consulting preferred
  • Ideally3+ years Clinical, Pharmaceutical or Medical Device experience with deep understanding of Research and Development; or 5+ Years working in a customer facing role, ideally with an agency providing services into the Pharma/ Medical Device industry.
  • Experience in shaping and managing multiple projects at the same time

About Regeneron Pharmaceuticals

Regeneron Pharmaceuticals is focused on the development of pharmaceutical products for the treatment of serious medical conditions.

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