Medical Research Council (MRC) Unit, The Gambia – We are the leading
research centre in sub-Saharan Africa, carrying out internationally
competitive research into tropical medicine for over 50 years. Our
current research agenda focuses on three themes: Disease Control &
Nutrition; Vaccines & Immunity. Looking towards the
future. we are aiming to push forward into new and challenging areas
reflecting changes in national and global health priorities.
We are recruiting to fill the position below:
Job Title: Research Clinician HIPC
- Established in 1947, the Medical Research Council Unit The
Gambia has an international reputation for ground-breaking research into
some of the leading causes of morbidity and mortality in the tropics.
Achievements include a large trial showing the efficacy of Haemophilus
influenzae type b vaccine in The Gambia and the subsequent near
elimination of the disease, pioneering studies of the impact of
insecticide treated bed nets as a preventive measure against malaria
leading up to their worldwide use, studies demonstrating the impact of
conjugate pneumococcal vaccines on pneumonia and child mortality and the
demonstration of a dramatic reduction in the carriage of Hepatitis B
in The Gambia due to the effects of vaccination.
- To reflect global health priorities and consequent international
funding opportunities the current research portfolio of MRC Unit The
Gambia is organized under three themes: Vaccines and Immunity, Disease
Control & Elimination and Nutrition. Cross-cutting these themes are
research in Maternal and Neonatal Health and an expanded research focus
across West Africa. Non-communicable diseases, particularly those
which are infection-related, are another area of work which is expected
to expand. These themes have been selected to target national health
needs, to reinforce sub-regional and international links and to address
some of the major priorities of the post-2015 Sustainable Development
- The Unit has an established clinical trials support office
(CTSO) and a research governance manager who provide advice on the
conduct of clinical trials and other clinical research and who provide
professional leadership and training. This includes support to address
the current regulatory environment in relation to Good Clinical
Practice, the regulatory requirements in The Gambia, the EU Clinical
Trials Directive and other internationally recognised standards for
clinical trial conduct. The research governance manager also oversees
the clinical trial sponsorship responsibilities taken on by The
- We are currently engaged in an ongoing series of clinical
vaccine trials ranging from phase 1 (including first-in-child and
first-in-infant cohorts) to phase 4 trials of various sizes, designs and
endpoints. The majority of trials are investigator-led and
internally-sponsored by the MRC Unit The Gambia although we also work
with other non-commercial and, on occasions, commercial sponsors.
- Recent trial have predominantly been undertaken in the Western
coastal region of The Gambia at established clinical trial facilities
within the compounds of government health facilities although future
trials will also be undertaken in other parts of The Gambia and also
potentially further afield.
- Many infections in young children and babies can be prevented by
giving vaccines to young babies, as we already do within the Expanded
Programme on Immunisation (EPI). However, many babies around the world
still die every year from infections. If we wish to make new vaccines to
change this situation, we need to better understand how babies’ bodies
defend themselves against infections. In the last few years, laboratory
tests including omic methods have become available which allow us to
have a much closer look at how the bodies’ protection works. These new
tests work with blood volumes small enough for us to take from newborns
and little babies. For this study along with our partners we are using
these omic methods to measure how EPI vaccines together protect babies.
The knowledge gained from this study may contribute to making better
early child vaccines in the future.
- Grade 2 – 30 – 32 points according to experience and
qualifications. Candidates with their FWACP Part 2 or equivalent, would
be Grade 2 – 32 points.
- Candidates with a directly relevant higher degree or with very
significant clinical vaccine trial research experience at least
comparable to either of the above might be considered for the higher
point (32 points)
Purpose of the Job
- To undertake or oversee all aspects of the study including
informed consent, assessing eligibility, collection of all data required
including safety data, completion of documentation and supervision of
the field team according to study protocol.
- To provide clinical assessment and care to study participants presenting with adverse events.
The post-holder will:
- Ensure that study objectives and methods are explained in an
appropriate language to potential study participants and/or guardians as
applicable, and informed consent is obtained prior to enrolment.
- Motivate, supervise, train and monitor the work of field team on
a daily basis to ensure that recruitment, clinical assessment, care,
and follow-up of study participants and collection of data and samples
are taken accurately, according to protocol and in a timely fashion. .
- Monitor treatment, progress of study participants if admitted for in-patient care.
- Undertake verbal autopsies if necessary to ascertain the cause of death of study participants, if any.
- As part of the recruitment procedures for this trial the
clinician will need to provide on-call cover at night and at weekends to
recruit participants and to assess any study subject who becomes unwell
out of hours.
- Strictly adhere to GCP guidelines, study protocol and MRCG
safety manual at all times. Ensure that confidentiality is maintained in
the collection and handling of information.
- Conduct the clinical assessment, investigation and care of study participants as may be required.
- Work on the Clinical Services on-call rota and provide clinical
support in the MRCG Outpatients Department on a rota basis and within
the confines of the work commitment required by the trial.
- The post-holder will be a full-time member of the MRC staff.
- The post-holder will report to Dr. Olubukola Idoko, Clinical Trial Coordinator.
- The theme Leader for the Vaccines and Immunity Theme and PI for the study is Professor Beate Kampmann.
- The Unit Director is Professor Umberto D’Alessandro.
- The Director of Operations is Mr Joan Vives Tomas.
- Appraisals are held at least annually.
Length of appointment:
- The appointment is for 2 years in the first instance and is subject to a probationary period of 6 months.
Any other duties:
- To perform any other duties consistent with the remit of the post.
- MBBS or equivalent.
- Experience of staff management
- Excellent interpersonal and verbal/written communication skills
- A flexible and well-organized approach to work and an ability to meet deadlines
- Attentiveness to detail
- Excellent written and spoken English
- Commitment to working in a multi-disciplinary team
- Excellent organizational skills
- Willingness to be on-call and work outside the normal working hours
- Practical experience of health research in developing countries
- Previous experience in conducting clinical trials according to ICH-GCP
- Clinical paediatric experience
- Record of publications in peer-reviewed journals
- Part 1/2 of FWACP or equivalent in paediatrics
- Postgraduate qualifications (Masters, Doctoral level)
- Excellent IT skills (Microsoft Word, Excel, Access).
- MRCG is an equal opportunities employer and operates a strict no smoking policy.
- Only short listed candidates will be contacted.
How to Apply
Interested and qualified candidates should send their applications to: [email protected] to obtain Application Form and a copy of the Job descriptions.
Application Deadline: 28th April, 2017.
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