The Ugandan Jobline

• Ensure that the study is implemented in
  compliance with the study protocol and that any deviations are properly
  documented and communicated.
• Actively
  participate in the development and adaptation of Standard Operating
  Procedures (SOPs).
• The
  incumbent will initiate and coordinate the process of obtaining
  study approval from the local Regulatory Authorities and Ethics Committee
  bodies, as applicable.
• Submit
  any substantial amendment of protocols or patient information and Informed
  consent forms for approval to the local Regulatory Authorities and
  Ethical bodies.
• Plan
  and execute the initial and continuous training of staff related to the
  study in coordination with the international principal investigator and
  study monitor.
• Ensure
  that all members of research team he/she is in charge of conduct the
  study in accordance to GCP regulations in agreement with protocol and
  study related SOPs.
• Maintain
  a Study Trial Investigator file containing all essentials documents.
• Record
  and promptly report Serious Adverse Reactions and other notifiable
  events to Sponsor, relevant local ethics and regulatory authorities.

• The
  applicant should be a Medical doctor with advanced training in clinical
  research, epidemiology or public health.
• Additional
  training in Good Clinical Practice.
• Registered
  with Medical and Dental Practitioners Council.
• Previous
  experience on clinical trial study implementation is an asset.
• Extensive
  knowledge of ICH guidelines, GCP, and the clinical trial study process.
• Ability
  to work effectively in teams as well as independently.
• Excellent
  verbal and written communication skills

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