Clinical Operations Manager
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Key skills for this role
About the Role
We are seeking a Clinical Operations Manager for a part-time, on-site role in Abu Dhabi. You will oversee clinical and research activities, coordinate study start-up, and ensure regulatory compliance.
Key Skills for This Role
Responsibilities
- Plan, coordinate, and monitor clinical operations for research projects and partnerships
- Supervise or collaborate with clinical research associates
- Coordinate study start up and documentation
- Maintain accurate records and reporting for internal and external stakeholders
- Align clinical workplans with broader policy and program goals
- Manage operational risks and troubleshoot issues during project implementation
- Contribute to protocol development
- Support ethical and regulatory submissions
- Foster strong relationships with clinical and institutional partners in the region
Requirements
- Strong clinical operations expertise, including experience in Clinical Operations and Clinical Research
- Experience working with or managing Clinical Research Associates
- Proficiency in Research and Project Management
- Knowledge of ethical, regulatory, and quality standards related to clinical research and human subjects protection
- Bachelor's degree in a health related, life science, or relevant field
- Demonstrated ability to work collaboratively with multidisciplinary teams and external partners
- Strong analytical, organizational, and documentation skills
- Excellent written and verbal communication skills in English
- Ability to work on site in Abu Dhabi
Full Job Posting
Role Description
- The Clinical Operations Manager is a part time, on site role based in Abu Dhabi, responsible for overseeing clinical and research related activities that support OGPD’s programs and initiatives.
- The person in this role will plan, coordinate, and monitor clinical operations for research projects and partnerships, ensuring that timelines, quality standards, and regulatory requirements are met.
- Day to day responsibilities include supervising or collaborating with clinical research associates, coordinating study start up and documentation, and maintaining accurate records and reporting for internal and external stakeholders.
- The Clinical Operations Manager will work closely with project teams to align clinical workplans with broader policy and program goals, manage operational risks, and troubleshoot issues that arise during project implementation.
- The role also includes contributing to protocol development, supporting ethical and regulatory submissions, and fostering strong relationships with clinical and institutional partners in the region.
Qualifications
- Strong clinical operations expertise, including experience in Clinical Operations and Clinical Research, with the ability to oversee day to day study conduct and site management.
- Experience working with or managing Clinical Research Associates, including coordination, guidance, and performance monitoring for clinical research activities.
- Proficiency in Research and Project Management, including planning, organizing, and tracking multiple clinical or research projects simultaneously.
- Knowledge of ethical, regulatory, and quality standards related to clinical research and human subjects protection.
- Bachelor’s degree in a health related, life science, or relevant field; an advanced degree or clinical background is an advantage.
- Demonstrated ability to work collaboratively with multidisciplinary teams and external partners, including academic, clinical, and governmental stakeholders.
- Strong analytical, organizational, and documentation skills, with attention to detail and a solutions focused approach.
- Excellent written and verbal communication skills in English; proficiency in Arabic is an asset.
- Ability to work on site in Abu Dhabi, manage part time hours effectively, and adapt to a mission driven, fast evolving environment.
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