Manager – Research Capability Building
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Key skills for this role
Role Overview
Lead the development of research capabilities within Fakeeh Care Group through policies, procedures, training programs, collaborations, disease registries, grant-linked training, and regulatory accreditation.
Enhance research excellence through talent development, process improvement, and collaboration across the organization and with external stakeholders.
Key Skills for This Role
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Job Purpose
Lead the development of research capabilities within Fakeeh Care Group through policies, procedures, training programs, collaborations, disease registries, grant-linked training, and regulatory accreditation.
Enhance research excellence through talent development, process improvement, and collaboration across the organization and with external stakeholders.
Strategic Leadership and Compliance
- Establish the Research Capability Building Unit strategic roadmap.
- Develop standard operating procedures and infrastructure to ensure compliance with ICH-GCP and regulatory requirements.
- Create medical research policies, IRB guidelines, scientific evaluation standards, and medical writing support guidelines.
- Develop registration and accreditation policies for SNIH, RDIA, AAHRPP, and international bodies.
- Oversee biobanking systems and disease registries.
Collaboration and Capacity Building
- Foster interdisciplinary collaboration across FCG units and external stakeholders.
- Represent FCG in national and international partnerships and promote multi-site research projects.
- Assess research skills and design training programs to increase the pool of qualified Principal Investigators.
- Collaborate with HCM and Fakeeh Academy on career development.
- Establish recognition and compensation mechanisms.
Communication and Special Projects
- Maintain communication between the Research Capability Building Unit, IRB, and CFGO.
- Develop strategies to promote research initiatives internally and externally.
- Lead grant-linked training programs, disease registries, biobanking systems, and volunteer research assistant programs.
- Develop research management system proposals.
- Assist with manuscript preparation and presentation of findings.
Requirements
- Minimum five years of experience in clinical trial management, 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.
- Excellent English proficiency.
Preferred Qualifications
- Arabic language proficiency is preferred.
- Clinical trial management certification such as SOCRA or ACRP certification is advantageous.
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