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Director Clinical Development

Job in Liverpool, Merseyside, L1, England, UK
Listing for: SRG
Seasonal/Temporary position
Listed on 2026-02-16
Job specializations:
  • IT/Tech
Job Description & How to Apply Below

1 day ago Be among the first 25 applicants

Sourcing Consultant @ SRG | Recruitment, Team Leadership

Clinical Development Director

Contract
: 18 Months

Therapeutic Areas
:
Neuroscience (3 roles) & Immunology (2 roles)

About the Role

We are seeking highly skilled Clinical Development Directors (CDD) to join global programs in Neuroscience and Immunology. This is a senior scientific leadership role, responsible for driving clinical development strategy and execution across late-phase trials (Phase 2 &
3).

Important:
  • This is not a Project Management role.
  • MDs are excluded; candidates must hold a PhD or Pharm

    D (Master’s considered, PhD strongly preferred).
  • No training provided – prior clinical development experience is essential.
Key Responsibilities
  • Lead and deliver clinical development activities for assigned program sections, including:
  • Clinical Development Plans (CDP), trial protocols, regulatory documents, and publications.
  • Provide scientific and clinical input into analyses, interpretation, and Clinical Study Reports (CSR).
  • Oversee clinical data review and ensure quality in collaboration with data management and biostatistics.
  • Contribute to regulatory submissions and responses to health authorities.
  • Support safety monitoring and reporting (PSURs, DSURs).
  • Represent clinical development in internal and external stakeholder interactions (KOLs, advisory boards, regulatory bodies).
  • Mentor and develop clinical team members; may lead a small team (approx. 3 reports).
  • Drive inspection readiness and quality standards across programs.
Ideal Background
  • Education:

    PhD or Pharm

    D in relevant field (Neuroscience preferred for Neuro roles).
  • Experience:
  • ≥7 years in clinical research/drug development (Phases I–IV), with ≥3 years in global clinical trial execution.
  • Strong late-phase experience (Phase 2 &
    3).
  • Therapeutic expertise in Neuroscience (Neurodegeneration, Neuroinflammation, Rare Diseases) or Immunology (Rheumatology, Dermatology acceptable).
  • Familiarity with Multiple Sclerosis, Huntington’s Disease, Myasthenia Gravis, or similar conditions is a plus.
  • Advanced knowledge of GCP, trial design, regulatory processes, and statistical principles.
  • Excellent communication, leadership, and stakeholder management skills.

Seniority level:
Director

Employment type:
Contract

Job function:
Science

Industries:
Pharmaceutical Manufacturing

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