Manager - Clinical Operations (SEHA Research Center)
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Key skills for this role
About the Role
SEHA Research Center is hiring a Manager of Clinical Operations to oversee daily clinical research activities across healthcare facilities. The role involves project management, policy development, compliance, staff supervision, and budget monitoring.
Key Skills for This Role
Responsibilities
- Overseeing the day to day clinical activities of research operations teams across HCFs
- Central oversight and management of project tracking – status, timelines, milestones, budget, scope, recruitment, quality, mandatory reporting across HCFs
- Developing, implementing, and evaluating clinical operations policies and SOPs and procedures
- Ensuring compliance with healthcare laws, regulations, and the facility’s policies
- Collaborating with HCF medical and administrative staff to ensure the delivery of high quality research operations
- Develop & implement initiatives to build efficiency in trial process, timelines and resources
- Organizing staff allocation to projects and evaluating performance
- Conducting regular staff meetings and providing training and development opportunities
- Guide and support team in management of trial issues and escalations related to feasibility, start up, recruitment, resourcing, CAPA, etc.
- Developing tools to track and manage team and project performance and utilization
- Monitoring budgets and managing resources effectively
- Participate in key BD meetings with clients to present research capabilities, expertise
Requirements
- Bachelors degree in Medicine, Pharmacy/Nursing or other medical fields; Masters degree preferred
- 10+ years of experience in Clinical research operations, including site management and coordination of global Phase I III clinical trials
- Excellent communication (written & verbal; English & Arabic) and interpersonal skills
- Ability to work collaboratively with cross functional teams and external partners
- Strong ability to track, project manage and coordinate projects activities across HCF
- Possess strong computer skills (MS Power Point, MS Excel, MS Word, MS Access, MS Outlook)
- Experience in regulatory compliance and data management is essential
Full Job Posting
Responsibilities
- Overseeing the day to day clinical activities of research operations teams across HCFs.
- Central oversight and management of project tracking – status, timelines, milestones, budget, scope, recruitment, quality, mandatory reporting across HCFs
- Developing, implementing, and evaluating clinical operations policies and SOPs and procedures.
- Ensuring compliance with healthcare laws, regulations, and the facility’s policies.
- Collaborating with HCF medical and administrative staff to ensure the delivery of high quality research operations.
- Develop & implement initiatives to build efficiency in trial process, timelines and resources
- Organizing staff allocation to projects and evaluating performance.
- Conducting regular staff meetings and providing training and development opportunities.
- Guide and support team in management of trial issues and escalations related to feasibility, start up, recruitment, resourcing, CAPA, etc.
- Developing tools to track and manage team and project performance and utilization.
- Monitoring budgets and managing resources effectively.
- Participate in key BD meetings with clients to present research capabilities, expertise
Qualifications
- Bachelors degree in Medicine, Pharmacy/Nursing or other medical fields with a preference for Masters degree in any of these disciplines.
- 10+ years of experience in Clinical research operations, including site management and coordination of global Phase I III clinical trials.
- Excellent communication (written & verbal; English & Arabic) and interpersonal skills, with the ability to inspire and influence others.
- Ability to work collaboratively with cross functional teams and external partners.
- Strong ability to track, project manage and coordinate projects activities across HCF.
- Possess strong computer skills (MS Power Point, MS Excel, MS Word, MS Access, MS Outlook)
- Experience in regulatory compliance and data management is essential.
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