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Manager – Research Capability Building

Fakeeh Technologies Pvt Ltd
Jeddah, KSA
Full-time
Senior
Onsite
Discovered 1 weeks ago
Clinical trial managementResearch capability buildingICH-GCP complianceResearch policy and SOP developmentInstitutional Review Board (IRB) guidelinesClinical research accreditation

Full Job Posting

Job purpose

Leads development of research capabilities within Fakeeh Care Group through policies, procedures, training, and collaborations.

Supports disease registries, grant-linked training, and regulatory accreditation while improving research talent and processes.

Strategy, policy, and compliance

  • Establish the research capability unit’s strategic roadmap and develop SOPs and infrastructure for ICH-GCP and regulatory compliance.
  • Create medical research policies, IRB guidelines, scientific evaluation standards, and medical writing support guidelines.
  • Develop policies for registration and accreditation with SNIH, RDIA, AAHRPP, and other relevant bodies.
  • Oversee biobanking systems and disease registries.

Collaboration and capacity building

  • Foster interdisciplinary collaboration across group units and with external stakeholders; represent the group in national and international partnerships.
  • Promote multisite research projects, assess research skills, design training, and increase the pool of qualified Principal Investigators.
  • Collaborate with HCM and Fakeeh Academy on career development and establish recognition and compensation mechanisms.
  • Maintain communication between the research capability unit, IRB, and CFGO; promote research initiatives internally and externally.

Special projects and post-trial services

  • Lead grant-linked training programs, disease registries, biobanking systems, and volunteer research assistant programs.
  • Develop research management system proposals and assist with manuscript preparation and presentation of findings.

Experience and education

  • At least five years of clinical trial management experience, including CRO and operational leadership experience.
  • Bachelor’s or master’s degree in Clinical Research Administration, Nursing, Public Health, Science, Medical Laboratory Sciences, or a related field.

Skills, language, and certification

  • Excellent English proficiency; Arabic is preferred.
  • Clinical trial management certification such as SOCRA or ACRP is advantageous.
  • Leadership, team-building, communication, collaboration, organizational, and problem-solving skills.

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