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Manager – Research Capability Building

Fakeeh Care Group
Jeddah, KSA
fulltime
Director
1 months ago
LeadershipStrategic PlanningBudgetingTeam ManagementPerformance ManagementProject Management
Free

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Job Purpose

Leads the development of research capabilities within Fakeeh Care Group (FCG).

Promotes research policies, procedures, training programs, and collaborations.

Supports disease registries, grant-linked training, and regulatory accreditation.

Enhances research excellence through talent development, process improvement, and fostering collaborations.

Key Responsibilities And Duties

  • Strategic Leadership: Establishes RCBU strategic roadmap. Develops SOPs and infrastructure to ensure compliance with ICH-GCP and regulatory requirements.
  • Policy Development: Creates medical research policies, IRB guidelines, and scientific evaluation standards. Designs medical writing support guidelines. Promotes research policies across FCG.
  • Accreditation & Compliance: Develops policies for registration/accreditation with SNIH, RDIA, and international bodies (AAHRPP). Oversees biobanking systems and disease registries.
  • Collaboration: Fosters interdisciplinary collaboration across FCG units and external stakeholders. Represents FCG in national/international partnerships. Promotes multi-site research projects.
  • Capacity Building: Assesses research skills, designs training programs, and increases pool of qualified Principal Investigators. Collaborates with HCM and Fakeeh Academy on career development. Establishes recognition and compensation mechanisms.
  • Communication: Maintains regular communication between RCBU, IRB, and CFGO. Develops strategies to promote research initiatives internally and externally.
  • Special Projects: Leads grant-linked training programs, disease registries, biobanking systems, and volunteer research assistant programs. Develops research management system proposals.
  • Post-Trial Services: Assists with manuscript preparation and presentation of findings.
  • Other duties as assigned within the scope of the job.

Requirements

  • Experience: Minimum 5 years in clinical trial management, with CRO and operational leadership experience.
  • Education: Bachelor’s/Master’s in Clinical Research Administration, Nursing, Public Health, Science, Medical Laboratory Sciences, or related fields.
  • Language: Excellent English proficiency; Arabic preferred.
  • Licenses / Certifications: Certification in clinical trial management (SOCRA, ACRP) advantageous.

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