Sacha Lynch

Regulatory Affairs Manager, Medicines

Sacha leads the regulatory medicines team and ensures that projects meet their objectives and are delivered efficiently and on budget.

Value to clients

Sacha brings knowledge of strategic R&D. She is readily able to identify efficiencies in product development and advise on optimal strategies to navigate the regulatory pathway for timely and valued product commercialisation for clients. She has actively managed regulatory departments focused on European registrations and developing regulatory strategies for optimal product development and lifecycle management.

  • A strong skill set in project management
  • Wealth of knowledge in generics industry
  • A proven track record in product development.

Experience

Sacha has over 15 years’ experience in regulatory affairs with skills in project management and leadership. She has worked in a worked in a variety of therapeutic areas including small molecules and niche products. Sacha has a track record in project management, leadership, mentoring, training and coaching as well as being well versed in working with key stakeholders across key business units supporting product and business development and Pharmacovigilance requirements. Among her many achievements, she has improved regulatory compliance by adopting processes and procedures and optimising communication procedure. This experience is complemented by an educational background in pharmacology and clinical research and being the proud holder of an Masters in Clinical Research Management from Cranfield University.

Other things about Sacha

  • Knowledge of and interest in managing GDP compliance
  • Project managing European procedures from the start through to launch planning
  • A keen Interest in commercial drivers to product development.
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