Monday 24 May 2021

Assistant Study Coordinator (KEN SHE Study) at Kenya Medical Research – KEMRI

Kenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya.

KMR6 Vacancy No. FN01-05-2021)

K MR6 Vacancy No. FN-10-03-2021

Reports to: Study Coordinator

Duration: 1 Year Renewable Contract as per KEMRI Scheme of Service. The first 3 months is a probation period

Duties and Responsibilities

  • Plan and coordinates the initiation of research study protocol, and the establishment of operating policies and procedures.
  • Plan, implement, supervise and conducts routine assessment of data collection and analysis systems in support of research protocol
  • Ensures the smooth and efficient day-to-day operation of research and data collection activities.
  • Coordinate the day-to-day activities of any technical support staff.
  • Assist in preparation of study initiation and monitoring visits
  • Assist in Regulatory binder assembly and maintenance
  • Recruitment and retention of study subjects
  • Assist study’s community engagement processes
  • Assist in staff training on the protocol related topics
  • Responding to priority mails, and participate in inter site calls and conferences
  • Assist in submission of the protocol to IRBs and renewals
  • Liaise with the study coordinator on reporting study related safety issues and reports and resolution of queries that may arise.
  • Attend to Staff HR related issues in liaison with the HR department
  • Drafting, reviewing and implementation of SOPs.
  • Assist on planning for orientation of new staff

Required Qualifications

Bachelor of Science or an equivalent Degree in Medicine, Nursing, Public Health or relevant field

Experience

  • Two years’ experience in clinical trials management and coordination
  • Experience with supervising research for public health or clinical studies

Desirable Qualities

  • Prior leadership experience managing research teams preferred
  • Experience with community health initiatives preferred
  • Experience with research studies or programs focused on senior citizens
  • Exceptional verbal and written communication skills
  • Fluency in English and Kiswahili
  • Ability to work effectively independently and as part of a team
  • Ability to effectively handle multiple priorities and organize workload
  • Excellent time and resource management skills
  • Ability to work with tight timelines and meet deadlines
  • Ability to manage and supervise a multi-disciplinary team
  • Ability to plan, initiate, coordinate and enforce protocols, policies and procedures
  • Experience using computers for a variety of tasks, including proficiency in organizing conference calls and typing to record meeting minutes
  • High level of competency in Microsoft applications including Word, Excel, and Outlook

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