The trial manager is responsible for the day-to-day coordinating, managing, and overseeing of Implementation of the different components of the trial.

Roles and responsibilities
• Taking part in site assessments and preparation before the trial
• Obtaining all relevant approvals prior to the start of the trial
Taking part in training of study personnel before the trial
4. Ensuring implementation of the trial according to the approved protocol and interface with the Pi of the trial and other investigators
• 5. Working with the relevant trial teams, i.e., qc, clinical team to ensure that trial related Documents and sops are documented and properly filed
• 6. Provision of regular and ad hoc information, both written and verbal, to all the trial participants And sponsors, to include reports, updates, guidance, and preformed commitments.
7. Planning and coordination of required trial meetings including scheduling weekly trial Implementation meetings
• 8. Preparation of progress reports
• 9. Managing the trial budget including initiating requisitions and working with the finance team To ensure proper accountability of advanced funds
• 10. Ensuring that all trial logistics (materials supplies and equipment) are available at the right time And in the right quantities
11. Supervising all trial personnel and ensuring that they deliver on the responsibilities
• 12. Participating in trial dissemination efforts including report writing
• 13. Managing correspondences with the trial stakeholders (sponsor, irb, nda, uncst, monitors Etc.)

Qualifications, skills and experience
• Mbchb, nursing degree or any other related health related degree.
• Postgraduate qualification in public health, epidemiology or any other related field
• Knowledge of regulatory requirements & good clinical practices (gcp)
• Clinical trials research experience
• Proficient with microsoft office word and excel
• Excellent written and verbal communication skills