Medical Research Council Unit The Gambia - The MRC Unit The Gambia at London School of Hygiene and Tropical Medicine (LSHTM) is one of two research units established in sub- Saharan Africa by the Medical Research Council UK and is the MRC Unit The Gambia at LSHTM’s single largest investment in medical research in a low and middle income country. MRC Unit The Gambia at LSHTM represents a unique concentration of scientific expertise and high quality research platforms in the West African region.
Location: Fajara, Gambia Department / Division: Research Support Office Grade: 2 - 35 Points
Length of appointment: The appointment is for 1 year (with possible extension to 3 years) and is subject to a probationary period of 6 months.
Introduction
The Medical Research Council Unit The Gambia is one of the largest scientific research centres in sub-Saharan Africa, with an international reputation for ground-breaking research into some of the leading causes of morbidity and mortality in the tropics.
Our overall goal is to improve the health of people in developing countries by aiming for excellence in research, healthcare and training.
Our research program spans basic scientific research, clinical studies, epidemiological studies and intervention trials, and translational research.
The field and laboratory-based work draws on excellent research and clinical facilities and attracts international funding.
To reflect changes in national and global health priorities and new international funding opportunities a new research portfolio has been organized under three themes:
Disease Control & Elimination;
Vaccines & Immunity; Nutrition &
Planetary Health.
These themes have been selected to target health needs of low- and middle-income countries, to reinforce sub-regional and international collaborations and to address some of the major current priorities in the Sustainable Development Goals.
The Unit, led by Professor Umberto D’Alessandro, receives an MRC core investment grant every 5 years, following the review of past activities and future plans.
In addition, all research activities are supported by external grants from a variety of sources.
The Unit has a turnover of more than £22m per annum and employs about 1,400 staff.
The Unit has a Clinical Trials Unit to conduct and advise others on the conduct of clinical research, to provide professional leadership and training in clinical trials, including support to address the current regulatory environment in relation to Good Clinical Practice and the EU Clinical Trials Directive.
The post-holder may be based at MRC Fajara or elsewhere in The Gambia according to the needs of ongoing trials.
Purpose of the Job
To support the Principal Investigator (PI) in all aspects of the management of the study and assume partly responsibilities of the PI when delegated
To be a focal point for communication with the sponsor and study team.
To oversee the development of study specific procedures and other trial documents required for trial conduct and to provide input into protocol development when required.
To oversee the daily conduct of the study at the trial sites.
To ensure the rights and safety of trial participants are maintained as paramount by all trial staff
To oversee the quality and consistency of all trial data entered into CRF/eCRF as specified in the study protocol and relevant study specific procedures
To oversee the training and supervision of the trial team staff including research clinicians, nurses, field workers, clinical trial officers, laboratory and data personnel
Work in partnership with the Clinical Trials Unit
To maintain the trial master file/investigator site file
Role
The post-holder will:
Know, understand and follow the study protocol at all times
Establish appropriate procedures required for effective running of the clinical trial such as study specific procedures and source documents.
Ensure that study objectives and methods are explained adequately to the clinical trial team and train nurses and field workers in the conduct of the study.
Manage the study staff and motivate, supervise and monitor the work of the clinical trial team on a daily basis to ensure that recruitment, clinical assessments, medical care and follow-up of study participants are conducted smoothly and that collection of data and samples are taken accurately according to protocol and in a timely fashion.
Ensure that the trial is conducted strictly according to ICH-GCP guidelines with respect to quality and ethics including confidentiality.
Oversee the review of all source data before entry into the dedicated database and follow-up queries.
Monitor the conduct of the trial by reviewing the assessment of clinical and safety data.
Coordinate the work of the clinical and laboratory study team
Undertake all work strictly following the safety guidelines as laid down in the MRC’s Safety Manual.
Manage the trial master file in conjunction with the PI
Provide limited clinical services at the study health centres or MRC clinic, when feasible in accordance with the required work for the trial.
S/he will oversee the daily conduct of the study, supervise the data entry into the CRF/eCRFs, supervise the study team of Clinicians, Nurses and Field Workers.
S/he will be the focal point for communication with the study team.
Relationships:
The post-holder will be a full-time member of the MRC staff.
The post-holder will report to Prof Umberto D’Alessandro, the PI of the trial, or to Dr Annette ERHART, co-PI and Malaria Research Coordinator at the MRC Unit;
The Unit Director and Theme Leader for the Disease Control & Elimination Theme is Professor Umberto D’Alessandro.
The Director of Operations is Dr Davis Nwakanma.
Appraisals:
Appraisals are held at least annually.
Any other duties:
To perform any other duties consistent with the remit of the post.
Person Specification
Education and Training - minimum requirements:
MB BS or equivalent medical qualification
FWACP or comparable Masters Level training in the field of clinical trials and/or vaccinology or comparable clinical trial hands-on experience
Previous work on clinical trials of drugs/vaccines following GCP requirements
Experience of clinical vaccine trials in a relevant setting
Practical experience of health research in developing countries
Experience of staff management
Excellent written and spoken English
Commitment to working in a multi-disciplinary team
Excellent interpersonal and verbal/written communication skills
A flexible and well-organized approach to work and an ability to meet deadlines
Excellent organisational skills
Excellent IT skills (Microsoft Word & Excel, in particular)
A team player and motivator
Willingness to be on-call and work outside the normal working hours.
Desirable:
Record of publications in peer-reviewed journals
Ability to work on databases and statistical packages.
Experience & Job related knowledge:
Previous work on clinical trials of drugs/vaccines following GCP requirements
Practical experience of health research in developing countries
Experience of staff management
Excellent written and spoken English
Abilities & Aptitudes:
Commitment to working in a multi-disciplinary team
Enthusiastic and committed team player and team motivator
Excellent interpersonal and verbal/written communication skills
A flexible and well-organized approach to work and an ability to meet deadlines
Attention to details
Excellent organizational skills
Other:
Willingness to be on-call and work outside the normal working hours.
Preferred:
Ability to work on data bases and statistical packages
Record of publications in peer-reviewed journals
Excellent IT skills (Microsoft Word, Excel, Access).
Remuneration
The salary will be on Grade 2, 35 Points of MRCG at LSHTM’s pay scale.
A minimum net monthly salary of 95,000 Dalasi is on offer. This equates to 1,860 USD approximately per month using the prevailing Dalasi / USD exchange rate.
Please note that the salary will be paid in Dalasi and that the USD figure quoted is only given as a guide.
For displaced staff the package will include rent-free furnished accommodation, flights, displacement allowance for spouse and children, contribution to school fees for children and shipment of personal effects.
Application Closing Date
21st February, 2022.
Method of Application
Interested and qualified candidates should please download the "Application Form" below. Completed Application forms and Documents should be e-mailed to: recruitment@mrc.gm using the Job Title as the subject of the mail.
Please check your qualifications against the requirements displayed in the position description since only those applicants that meet the requirements will be considered.
You are therefore strongly encouraged to apply only to an advertised vacancy notice for which you consider you possess the required qualifications, skills and knowledge.
Decisions regarding which candidates are selected for interview are based upon the information that you provide in your application form. It is advisable to retain a copy of your completed application form in the event that you need it to help you prepare for interview.
MRCG at LSHTM is an Equal Opportunities Employer and operates a strict no smoking policy.
MRCG at LSHTM does not contact applicants to confirm the receipt of completed application forms.
Due to the number of applications received, it is MRC policy to contact shortlisted candidates only.
Application forms not received by the stipulated deadline will not be submitted for shortlisting.
If you do not hear from us within five weeks of the closing date, you should assume that your application has been unsuccessful.