Centre for Microbiology Research
KEMRI - RCTP
Opening Date: 17th May ,2021 Closing Date: 7th June,2021
Study Description
The KEN SHE Study is a prospective, blinded randomized study that will test the efficacy of
single-dose bivalent and nonavalent HPV vaccination as a catch-up strategy.
1. Position: Assistant Study Coordinator (Position 1) KMR6 Vacancy No. FN-
01-05-2021) K MR6 Vacancy No. FN-10-03-2021
Reports to: Study Coordinator
Location: Kisumu
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
2. Position: Research Data Manager (1 Position) KMR6 Vacancy No. FN-02-
05-2021) K MR6 Vacancy No. FN-10-03-2021
Reports to: Study Coordinator
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Overseeing daily data activities
Oversee data clerks duties
Conduct training of all data clerks and relevant staff on data specific items,
study protocol, SOPs and documents, equipment use
Creating and maintaining all study database
Updating and overseeing databases updates
Generating study summaries and reports as required
Arranging screening, enrolment and follow up files for daily schedules
Performing QA/QC of electronic and paper Case report forms (CRFs),
clinical chart notes and name chart, ensures competency at all QC levels
Printing CRFs and arranging them in study binders
Faxing and refilling of CRFs as needed
Communicates with CC on behalf of data in relation to QC, supplies, CRFs
updates and changes in CRFs.
Spearheads the randomization process and ensures the process is smooth
Ensures Label printing and delivery to the clinic team
Spear heads analysis and resolution of DFNet queries
Organizes eligibility meetings, tracks the screen/enrollment participant status
records and provides daily reports.
Develops all data related SOPs
Assist staff in data analysis e.g. abstract writing
Ensures data printers and data fax machines are maintained and stored well.
Maintain data supplies inventory
Manage study data
Tracking of all study documents, data and storage
Ensures archival procedures of all study data, hard and soft is secured and
stored well
Ensures confidentiality and safe storage of all participant identifying materials
like link logs are kept confidentially.
Gives QA/QC monthly and weekly reports
Provide weekly site data reports
Ensure biometric data capture of all study participants- configuration and
programming, registration and verification of participants.
Required Qualifications
Bachelor’s Degree in Statistics/ Applied Statistics/Biostatistics/Computer
science
Conversant with statistical packages i.e. Stata, SPSS, R, SAS.
Conversant with data management databases i.e. MS access, Excel SQL or
Visual basics.
Basic IT skills i.e. Software installations, printer installations and trouble
shootings.
Having experience with data fax transmission machine is an added advantage.
Experience
At least two (2) years Clinical research experience is an added advantage
Desirable Qualities
Leadership skills to promote creativity and innovation.
Excellent verbal and written skills, good organizational, interpersonal, and
team skills.
Applicable knowledge working with other clinical databases e.g. SAS, etc.
Experience with working on Phase I- IV study trials within a clinical set up.
Organizational and time management skills.
Must have strong written and verbal communication skills, project
management skills, computer skills, and database skills.
Ability to lead a team of workers
3. Position: Study Nurse (4 Positions) K MR 7 Vacancy No. FN-03-05-2021
Reports to: Study Doctor
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme of
Service. The first 3 months is a probation period
Duties and Responsibilities
Register and consent study participants and assist with eligibility
determination, screening and enrolment of study participants.
Informed Consent administration per study protocol and collection of
participant medical and surgical history.
Work in consultation with the study clinicians in all steps above
Participant vaccination and psychosocial counselling
Prescreening and screening of participants
Support in health talks to participants at the clinic and mobilization sources.
Collect nasal swab specimens and phlebotomy.
Observe participants after vaccination and report any AEs observed to study
doctor.
Ensure participant flow at the clinic.
Respond to questions about the study posed by participants and the
community in consultation with the study doctor.
Ensure participant retention and adhere to site retention strategies.
Maintain a good relationship with the community, study participants and other
clinic staff.
Maintain up to date participant visit notes
Administer Case Report Forms (CRFs), accurate recording of data on CRFs
and perform self QC
Assess adherence to study products- vaccine schedules and take anthropometric
measurements
Perform home visits.
Develop and review clinic related SOPs
Laboratory results interpretation
Prepare weekly and monthly progress reports of personal study activities
Closely work with other staff members to ensure the success of the study
Required Qualifications
Diploma in Nursing
Must be registered with the Nursing officers council of Kenya.
Experience:
Knowledge and experience in vaccine administration and psychosocial
counselling
Good Clinical Practice training/Human Subjects Protection training
At least two (2) years Clinical research experience
Desirable Qualities
Commitment to integrity and high quality performance
Good interpersonal skills and ability to work in a team
Keen and attentive to detail
Ability to follow instructions and procedures
Articulate in both verbal and written communication in English and Swahili.
Counseling skills
Computer literacy
4. Position: Receptionist (1 Position)) K MR 7 Vacancy No. FN-04-05-21
Reports to: Retention Officer
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
• Receive and welcome all visitors to the study clinic
• Receive and welcome referred participants for screening and possible
enrollment and follow up visits.
• Schedule appointments with participants.
• Organize in liaison with the clinic lead and Outreach coordinator, schedules for
study participants
• Counter-checking completeness of locator information forms after
screening/enrollment and during follow-up visits.
• Facilitate efficient participant flow within the clinic.
• Receive all external and internal calls to the reception.
• Receive parcels and direct them to respective staff
• Write regular reports on the participant clinic flow, appointments and
reimbursements.
• Maintain participant schedule database, re imbursement and ensure they are
refreshed and comfortable as they wait.
• Observe participants’ and visitors’ traffic within the clinic
• Receive all parcels delivered at the reception, track and disburse appropriately
• Maintain the study participant link log and all registers, diaries and appointment
cards, ensuring confidentiality and safe storage of these documents
• Updating participant link log
• Communicate well with all visitors at the reception including study
participants. Chanel all issues raised appropriately
• Take minutes during study site meetings and send them out on time
• Liaise with the PI and maintain her diary
• Facilitate study regulatory approvals, forwarding submission package to
SERU/PPB and follow up of the approvals with the Nairobi CMR office
• Ensure participant retention
Required Qualifications
Minimum diploma in Secretarial, Front Office Administration, hospitality or
any other relevant courses
Excellent knowledge and extensive experience in computer applications, MS
word, Excel, and access
Experience:
At least two (2) years Clinical research experience
Desirable Qualities
Organizational and time management skills.
Must be a good communicator, good listener, patient, proactive and with vast
knowledge in Public relation
Excellent social and public relations skills
Computer literacy
Data entry skills
Ability to follow instructions, good listener, honest and attention to detail
Fair Knowledge and experience in finance and budgets
5 .Position: Research Driver (1 Position) K MR 8 Vacancy No. FN-05-05-2021
Reports to: Study Administrator
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Safely drive the vehicles as assigned
Ensure compliance to the road Traffic Act
Carry out daily routine checks on the vehicle before driving out.
Ensure maximum security of vehicle and its accessories under his
charge.
Ensure safety of passengers and cargo under his charge.
Monitor condition and performance of vehicle and promptly report to
superiors.
Carry out minor repairs and adjustments on the vehicle, and maintain
their cleanliness.
Take vehicle for servicing and repairs as directed by the superior.
Maintain a record of movements for the vehicle assigned to him.
Submit reports on vehicle movements and mechanical conditions as
requested
Report any accidents experienced to the administrator within the same
working day of occurence
Offer transport to study visitors
Transport staff members to various outreach activities
Picking potential participants to study clinic from collaborating
recruitment sources
Transporting study participants to specialized clinics or hospitalization
Assist in purchase and delivery of study supplies as needed
Transporting subjects, locating/tracing them where necessary.
Shipment of study participants samples to respective laboratory
Assist in distribution of study recruitment materials
Required Qualifications
O-Level School Certificate.
Valid Driving License class BCE
Certificate of Defensive Driving Course will be added advantage.
Current Certificate of Good conduct
Basic Automotive Mechanical skills and sound knowledge about
vehicles.
Experience
At least Three years proven experience as a driver on highways
Desirable Qualities
Must be a good communicator, good listener, patient, proactive and
can follow instructions.
Good eye sight, neat and good interpersonal skills
Good knowledge of the local community and traffic
Experience in courier or shipment of biological specimens
6. Position: Study Administrative officers (2 Positions) K MR6 Vacancy No.
FN-06-05-2021
Reports to: Study Finance Manager
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Imprest reconciliations and management
Petty cash management
Bank reconciliations
Monitor budget through expenditure tracking
Prepare variance reports
Assist in facilitating trainings & conferences
Monitor & ensure payments for vendors are actualized
Manage contracts & agreements between the Program & other service
providers
Asset register management
Assist in Inventory management
Support in study related procurement processes and tracking of supplies
Required Qualifications
• B.com. Degree (Finance/Accounting option), Business Administration or
equivalent
• CPA (II) or Equivalent
Experience
• Minimum of 3 years’ experience in a busy organization
• Experience working in research organization is an added advantage
Desirable Qualities
• Advanced computer skills on MS Office, accounting software packages
• Ability to manipulate large amounts of data and to compile detailed reports
• High attention to detail and excellent analytical skills
• Knowledge and experience in Procurement and supplies
• Good presentation skills. 1 Position) K MR6 Vacancy No. FN-08-03-2021
7. Position: Data Clerk (Position 3) K MR7 Vacancy No. FN-07-05-
2021
Reports to: Data Manager
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Updating study databases
Arranging screening, enrolment and follow up files for daily schedules
Performing QA/QC of electronic Case report forms (eCRFs), chart notes and
name charts to ensure quality and accuracy.
Printing CRFs, Consent forms as needed and arranging them in participant
binders
Maintain data supplies inventory
Study Data management and filling
Participate in participant randomization process
Updating participant link log
Label printing and delivery to the clinic team
Labeling data room, logs, books and files
Participate actively in the archival process of study data and ensuring proper
storage and maintenance of the same
Communicate closely with Data Manager to ensure priority tasks are completed
and to resolve any data or other related issues that arise
Ensure data entry computers and all equipment in data room are secure and
used appropriately.
Develop and review of data related SOPs
Required Qualifications
Diploma in ICT or computer related courses.
Experience in data entry and organization
Competency in using computer software applications like Microsoft Office
programs and familiarity with web-based programs, excel spreadsheets
required.
Experience
• Minimum of 2 years’ experience in a research organization and filed work
• Proven project management skills and experience of managing staff in social
science research projects, educational outreach or public engagement
initiatives
• Demonstrated experience of communication and coordination with education
stakeholders at all levels;
• Experience in conducting mixed-methods social science research involving
the collection and analysis of qualitative and quantitative data;
• Excellent written communication skills
Desirable Qualities
Excellent interpersonal, teamwork, and communication skills.
Strong organizational skills.
Commitment to integrity and high quality performance.
Attention to details
Strong professional references from previous supervisors.
Above average computer applications experience and proficiency.
Ability to work in a clinically busy, resource-challenged, and demanding
environment
8. Position: Laboratory Technologists (3 Positions) K MR7 Vacancy No.FN
-08-05-2021
Reports to: Laboratory Manager
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Accurate and timely performing of Study specific assays
Nasal Swab collection of participants
Ensuring custody of participant specimens and storage/archival
Appropriate reporting of any abnormal lab result.
Ensure maintenance and troubleshooting on all lab equipment and report to
the supervisor
Running and logging of specimen controls as per the set SOP.
Ensuring Laboratory Waste segregation and management.
Developing and updating laboratory inventory.
Developing and continuous review of standard operating procedures in
keeping with the protocol for the laboratory, and all lab related documents
and manuals.
Ensure compliance with all the SOPs and respective specimen flow charts
Projection on consumables and reagents, and re-ordering whenever due and
ensuring custody.
Participate and pass all required proficiency testing
Participate in timely enrolment of all EQAs required
Participate in supervised sample shipment procedures
Ensure that are IATA certified and compliant
Updating and ensuring quality assurance of the lab specimen data base
GCLP compliant
Receive, download, and post/report all external lab results/reports
Transcription of all lab results and communication of the same as per the lab
results communication SOP
QA/QC point persons at the lab level
Required Qualifications
Diploma in Medical Laboratory
Degree in Medical Laboratory, biomedical laboratory or biochemical
laboratory added advantage
Extensive and recent hands-on experience on running HIV-1, Pregnancy
testing, CD4 count, PCR, HIV ELISA assays and medical sample shipment.
Must have Good Clinical laboratory Practice training and/or CITI training.
Must be registered with KMLTTB with a valid Practicing Certificate.
Experience
At least two (2) years Clinical research experience in a busy research laboratory
setting
Desirable Qualities
Excellent written and verbal communication skills.
Extensive organization skills
Ability to work in a clinically busy, resource-challenged and demanding
environment.
Commitment to integrity and high quality performance
Good interpersonal skills and ability to work in a team
Keen and attentive to detail
Ability to communicate lab results , write reports and trouble shoot lab
equipment related challenges
Proactive, ability to work independently, interact well with other departments
Familiarity with a multi- department clinical lab setting
9. Position: Research Medical Officer (Position 1) K MR5 Vacancy No. FN-
09-05-2021
Reports to: Study Coordinator
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Administration and budget plans for the clinic department
Supervision – clinic staff and clinical activities, including duty allocation and
weekly Rota, ensure smooth clinical flow.
Staff training- Regular staff trainings and assessments on protocol, SOPs and
other study relevant materials
Participant safety- Assess participant eligibility, assess, monitor, track, grade
and report Adverse events/Serious Adverse events including laboratory
results
Participant recruitment and retention
Community and stakeholder engagement
Perform participant medical and physical examinations
Develop and review study SOPs, manuals and IEC materials
Quality control: Ensure high quality data collection and timely query
resolution by the clinical team.
Report writing and presentations : Prepare weekly and monthly progress
reports of clinic study activities
Required Qualifications
Experienced, practicing medical officer (MD/MBChB) with extensive and
recent hands-on experience and expertise in supervision.
Experience
Minimum 3 years professional clinical experience hands-on experience and
expertise in supervision
Desirable Qualities
Experience managing and supporting other staff in the professional field
Professional experience in emergency/disaster medicine, outbreak
management, Public Health, Pediatrics, Rural and remote medicine or other
relevant areas is an asset
Good Clinical Practice training/Human Subjects Protection training
Up to date with resuscitation and anaphylaxis including competent to give
intramuscular injections and subcutaneous administration of local
anesthetic
Experience working with pediatric, adult and geriatric patient populations
Ability to coordinate and deliver out-patient services in low-resource settings
Competent computer skills (Windows, Microsoft Office, spreadsheets, word
processing, e-mail)
Commitment to integrity and high quality performance
Building trust; Teamwork; Communication; Professionalism; Empowering
others; Diversity; Judgement/Decision-making.
10. Position: Community Tracker (Positions 4) K MR7 Vacancy No. FN-10-
05-2021
Reports to: Community Liaison Officer
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Community engagement
Community sensitization and mobilization for the study.
Work with CORPS to map study area and recruit potential subjects
Hold regular meetings and communication with local leaders and Community
Units
Network with stakeholders
Participate in accelerated mobilization (distributing flyers and posters and
conducting a mobile campaign with a public address system to mobilize the
community.
Liaise with community leaders, gatekeepers and the community members
about the study in consultation with the CLO.
Community Advisory Board formulation and continuously liaising with the
board
Participant recruitment activities
Conducting outreach activities and participant referral
Escorting participants home as needed
Counseling and informed consent process
Develop and review participant recruitment SOP and implement strategies
Participant referral to site
Participant retention activities
Obtaining and updating participant locator information
Report writing on recruitment and retention strategies and updating of the
community diary
Develop and review participant retention SOP and implement strategies
Participate in health talks at the site, community and health facilities
Participant physical and phone tracing as needed.
Participant home visits
Required Qualifications
Diploma in Community Health, Social Sciences, Social Work, Sociology,
Psychological Counselling or other related fields.
Experience in working in a busy clinical research set up with extensive hands-
on experience working in with communities and other stakeholders.
Experience
More than two (2) years Clinical Research experience
Good Clinical Practice training/Human Subjects Protection training is an
added advantage
Desirable Qualities
Commitment to integrity and high quality performance
Good interpersonal skills and ability to work in a team
Keen and attentive to detail
Ability to task-shift
Ability to work independently, team player, good communicator, respectful,
flexible, enthusiastic, innovative and proactive
Articulate in both verbal and written communication in English and Swahili.
Luo speakers have an added advantage.
Experience in mobilizing the community especially youth and women
organizations
Computer literacy
Counselling skills
11. Position: Clinical Officer (Position 1) KMR7 Vacancy No. FN-10-03-
2021Position) K MR6 Vacancy No. FN-10-03-2021
Reports to: Study Doctor
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme
of Service. The first 3 months is a probation period
Duties and Responsibilities
Register, consent study participants and assist with eligibility screening and
enrolment of study participants.
Prescreening of participants
Support in health talks to participants at the clinic and mobilization sources
Conduct physical and medical examinations for study participants.
Participant vaccination and psychosocial counselling
Perform phlebotomy and collect nasal swab specimen collection
Complete case report forms and work closely with the study doctor to report
all possible SAEs to the study safety monitor and KEMRI IRB.
Address safety queries raised by the study safety monitor
Conducts follow up visits on study participants.
Perform clinical assessments of participants, grading of symptoms/diagnoses,
interpret laboratory results and follow up
Carry out medical examinations and manage adverse events among study
participants.
Collect requisite study laboratory and pathological specimens
Prepare and counsel participants as per the study protocol.
Perform accurate record keeping and check study forms for completeness and
accuracy each day.
Participate in the eligibility criteria selection of study participants
Discuss participants follow-up schedule visits in collaboration with the
nursing desk and reception.
Respond to questions about the study posed by participants and the
community.
Maintain a good relationship with the community and other clinic staff.
In-depth understanding the logistics required to conduct of the study.
Report problems encountered to study Medical officer and consult
appropriately.
Assess adherence to study products by participants and institute appropriate
measures
Attend to the clinic help line
Contact participants with Adverse events, work with the Community team to
trace up these participants, counsel them, follow them up and accurately
document progress
Prepare weekly and monthly progress reports of personal study activities
Assist the study doctor in the development and review of clinic related SOPs
Continuously update clinic room inventory and safe keeping of all items in
the respective clinic rooms
Required Qualifications
Diploma in Clinical Medicine and Surgery
Holds a current practicing license Clinical Officers Council of Kenya
Experience
At least two (2) years Clinical research experience
Desirable Qualities
Demonstrated track record working in busy clinic
Knowledge and experience in vaccine administration and psychosocial
counselling
Strong interpersonal, communication, and listening skills
Must be able to work in a professional and ethical manner with competence,
accountability, and integrity
Basic computer skills
Detail-oriented
12. Position: Cleaner and Messenger (P o s i t i o n 2) K MR 11 Vacancy No.
FN-11-05-2021
Reports to: Study Administrator
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme of
Service. The first 3 months is a
probation period
Duties and Responsibilities
Provides efficient messenger services focusing on achievement of the
following results
Collection and delivery of mail and other materials as required from and
to the post office, courier and other institutions like Kenya power and
Safaricom/ Zain within town.
Sorting, delivery and pick up of mail from various offices on the
premises at regular intervals. Maintenance of records as required
Photocopying and duplicating services;
Ensuring that tea, water and refreshments are served and provided to
the study staff and official meetings as requested;
Assist in the loading, unloading and movement of furniture,
equipment and cargo office supplies;
Perform Variety of unskilled tasks as helper and messenger;
Remain flexible and work additional hours when required;
Other duties as required.
Provides efficient organization and cleaning services
Keeping clean the offices, kitchen, corridors, toilets, and training
venues and the office environment at all the times;
Paying attention and ensuring hygienic standard of sanitary facilities
at all the times;
Keeps office room floors, surfaces, furniture, walls, doors, windows,
curtains clean and hygienic;
Clean the toilets and to put in the toilets the toilet rolls, soaps, washing
liquid and hand towels when required;
Report on the stock status of toilet rolls, soaps, washing liquid etc.;
Maintaining the organization of paper, documents, and clean desks
and offices;
Supporting office hospitality in the presence of guests;
Maintaining cleanliness of the entrance and office environment
Required Qualifications
Minimum o-level
Experience:
At least 1 year of work experience preferably with a busy medical
organizations.
Desirable Qualities
Understanding of the study site operations, procedures and
requirements
Efficiency in the delivery of all listed services
Focuses on result for the site and responds positively to feedback;
Consistently approaches work with energy and a positive, constructive
attitude;
Responds positively to critical feedback.
Flexible
Preferred previous training in cleaning & tea service processes;
Quality oriented; Supportive; Timely; Personal organization;
knowledge of Hygiene; Ethical
S/he demonstrates a client-oriented approach, high sense of
responsibility, courtesy, tact and ability to work with people with
diverse backgrounds.
Applicants should attach the following:
• Letter of Application (Indicate Vacancy Number on the subject
line)
• Current Resume or Curriculum Vitae with Telephone number and e-
mail address
• Two letters of reference with contact telephone numbers
• Copies of Academic Certificates and Transcripts
• A copy of the latest pay slip (if applicable)
• A copy of National Identity card or passport
All applications to be done through email [email protected]
KEMRI or any of its programs, Studies or Projects does not solicit for Money or any form of reward for a Job applicant to be considered for employment. Any such requests should be immediately reported to the HR department. Canvassing will lead to automatic disqualification.
KEMRI IS AN EQUAL OPPORTUNITY EMPLOYER COMMITTED TO DIVERSITY; PERSONS WITH DISABILITY, WOMEN YOUTH AND THOSE FROM MARGINALIZED AREAS ARE ENCOURAGED TO APPLY.
only Shortlisted candidates will be contacted