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You are here : Home / / SITE LEAD (GSK MALARIA STUDY) & MEDICAL OFFICER (EPIMAL STUDY)

SITE LEAD (GSK MALARIA STUDY) & MEDICAL OFFICER (EPIMAL STUDY)

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      KAMUZU UNIVERSITY OF HEALTH SCIENCES

PHNG

  VACANCY ANNOUNCEMENT

The Kamuzu University of Health Sciences (KUHeS) is a new University formed by merging College of Medicine and Kamuzu College of Nursing and established by an Act of Parliament (No. 20 of 2019). It is a comprehensive health and allied sciences University and intends to train more health professionals that are globally competent but locally relevant.

The Public Health & Nutrition Research Group (PHNG) is a research unit within the School of Public Health and Family Medicine. PHNG’s mission is to advance research and knowledge in all their aspects and to promote high quality multidisciplinary and inter-professional research to shape local and international health policy, programs, and practices. The current research focus for PHNG is in maternal and child health research with a special focus on human growth, nutrition and the interactions between infection and nutrition. Other areas of interest include health systems, implementation science, food security, food systems research.

The University is inviting applications from suitably qualified candidates to fill the following positions:

  1. SITE LEAD (GSK MALARIA STUDY)

Role Overview

The PHNG GSK Malaria Mangochi Site Lead will be the overall coordinator responsible for the day to day management and coordination of the observational study to evaluate the safety, effectiveness and impact of the RTS,S/AS011E vaccine in young children at the Mangochi site which comprise the Mangochi and Monkey Bay clusters. As Overall Site Lead, he/she will be de-facto Co-Investigatorof the EPIMAL003 and EPIMAL005 study protocols.

The Site Lead will primarily be based in Mangochi with very frequent travel to Blantyre. He/she will report to the Principal Investigator and GSK Site Process Lead and other GSK appointed contractors.

 

Duties and responsibilities

  1. Oversee and coordinate day to day study activities at the site (includes Mangochi and Monkey Bay Clusters).
  2. Be primarily the budget holder at the site for all EPIMAL studies
  3. Plan and train study teams using ICH GCP guidelines, Institutional policies, local regulations, protocol and SOPs.
  4. Record and report Severe Adverse Events.
  5. Keep up to date the study investigators file at the site.
  6. Participate in the review of study Standard Operating Procedures.
  7. Lead in community engagement with assistance from the PI to ensure all community leaders are aware of the study activities.
  8. Ensure collation and distribution of all study related materials to study teams in line with the budget
  9. Organize and document action points from weekly study team meetings.
  10. Provide weekly and monthly study report.
  11. Conduct performance appraisals for staff under direct supervision.
  12. Identify knowledge and skill gaps for the study team and effectively plan training for them.
  13. Carry out any other relevant duties that may be assigned by the PI.

Minimum Requirements

  • MBBS degree with at least 5years’ clinical experience of which at least two years should be in Paediatric research.
  • Registered with Medical Council of Malawi and be certified in Good Clinical Practice (GCP) and Human Subjects protection (HSP).
  • Must be numerate and have good computer skills (Excel, Word, Zoom and Outlook),
  • Must have strong leadership, communication and research skills.

 

  1. MEDICAL OFFICER (EPIMAL STUDY)

Role Overview

The Medical Officer will be responsible for conducting clinical evaluations of study participants. The officer will also be responsible for reporting severe adverse events, adverse events of special interest, adverse events following immunizations and expedited adverse events. The medical officer will also facilitate resolution of queries and also ensure that all corrections made are reflected in the electronic information storage system (Inform).

The Medical Officer will be based in Mangochi. He/she will report to the Site Lead

Duties and Responsibilities

  1. Clinical evaluation of study participants
  2. Facilitate weekly resolution of safety queries.
  3. Draft and submit safety reports such as serious adverse events, protocol deviations and protocol violations to COMREC
  4. Report adverse events of special interest (AESI) to the sponsor in protocol specified time interval.
  5. Supervise and train clinical officers in diagnosis and management of AESI and Adverse Events Following Immunisation (AEFI).
  6. 6.    Any other duties as assigned by site lead, co-PI and PI as specified in the protocol delegation log.
  7. Provide feedback to Ministry of Health staff and other partners on patient care outcomes
  8. Facilitate study participant referral to tertiary facilities for diagnosis and management of disease   

Minimum Requirements

  • MBBS degree from a reputable institution with more than threeyears clinicalexperience and at least one year research experience.
  • Must have experience with Quality Control (QC) and Quality Assurance (QA)of research studies and must be certified in Human Subjects Protection (HSP) and Good Clinical Practice (GCP. Good computer skills (Excel, Word), leadership and communication skills and research skills.
  • Must be registered member of Medical Council of Malawi

How to Apply

Applicants meeting the requirements for any of the positions should submit applications including copies of certificates and a detailed CV with names, emails and contacts of 3 traceable professional referees, (one of which must be from the most recent or current employer) to:

The Registrar

Kamuzu University of Health Sciences

P/Bag 360

Chichiri

Blantyre 3

Or via email to: hr@medcol.mw

 

To apply for this job email your details to dmwenye@medcol.mw

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