Job description:
I. Obtaining informed patient consent from patient or family member
II. Filing of consent forms and Translation
III. Establishing and maintaining a positive relationship with study patients
IV. Chasing outstanding blood results (in conjunction with study doctors) and informing study doctor of results
V. Documentation of relevant clinical information in patient records
VI. Organising follow-up care on patient discharge
VII. ARV counselling of study patients and their treatment supporters
VIII. Maintain investigator site file (ISF)
OTHER TRIAL RELATED ACTIVITIES
1. Ordering trial equipment
2. Positive relationship building with all hospital staff.
3. Ensuring adequate supplies of IMP in conjunction with pharmacist and trial manager.
4. Ensure patient is linked in to local ARV treatment program following end of trial follow up period
Qualifications and experience
• Diploma in Nursing, Research experience will be an added advantage
• Preferably at least 2 years of experience in clinical trial research projects
• Managerial skills
• Expertise in field work
• Team player and motivator
I. Obtaining informed patient consent from patient or family member
II. Filing of consent forms and Translation
III. Establishing and maintaining a positive relationship with study patients
IV. Chasing outstanding blood results (in conjunction with study doctors) and informing study doctor of results
V. Documentation of relevant clinical information in patient records
VI. Organising follow-up care on patient discharge
VII. ARV counselling of study patients and their treatment supporters
VIII. Maintain investigator site file (ISF)
OTHER TRIAL RELATED ACTIVITIES
1. Ordering trial equipment
2. Positive relationship building with all hospital staff.
3. Ensuring adequate supplies of IMP in conjunction with pharmacist and trial manager.
4. Ensure patient is linked in to local ARV treatment program following end of trial follow up period
Qualifications and experience
• Diploma in Nursing, Research experience will be an added advantage
• Preferably at least 2 years of experience in clinical trial research projects
• Managerial skills
• Expertise in field work
• Team player and motivator
APPLICATION INSTRUCTIONS:
Remunerations:
Competitive attractive salaries attached to all posts depending on qualifications and experiences.
Mode of Applications
All applications should be enclosed with certified photocopies of relevant certificates and detailed curriculum vitae.Applicants are required to submit their applications not later than one week after the first appearance of this advertisement to the address below. Applicants are also reminded to indicate all contact information necessary with which information can reach them easily. Only shortlisted applicants will be notified. In case you do not here from us in two weeks time after the closing date consider yourself unsuccessful.
The Centre Director
National Institute for Medical Research
Muhimbili Medical Research Centre
P O Box 3436
Dar Es Salaam, TANZANIA.
e-mail: muhimbili@nimr.or.tz
Competitive attractive salaries attached to all posts depending on qualifications and experiences.
Mode of Applications
All applications should be enclosed with certified photocopies of relevant certificates and detailed curriculum vitae.Applicants are required to submit their applications not later than one week after the first appearance of this advertisement to the address below. Applicants are also reminded to indicate all contact information necessary with which information can reach them easily. Only shortlisted applicants will be notified. In case you do not here from us in two weeks time after the closing date consider yourself unsuccessful.
The Centre Director
National Institute for Medical Research
Muhimbili Medical Research Centre
P O Box 3436
Dar Es Salaam, TANZANIA.
e-mail: muhimbili@nimr.or.tz
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