NIMR – National Institute for Medical Research Jobs (11 Vacancies)

NIMR – National Institute for Medical Research Jobs (11 Vacancies)

BACKGROUND:

The National Institute for Medical Research (NIMR) is a Parastatal Organization established

by the Act of Parliament No. 23 of 1979 and became operational in 1980.

Integrated Care for HIV and Non Communicable diseases in Africa is a collaborative Research Study between National Institute for Medical Research Muhimbili Centre, Liverpool School of Tropical Medicine – UK, MRC/UVRI – Uganda, Makerere University, IDI & The AIDS Support Organisation (TASO) in Uganda, Diabetes Federation in Tanzania and Ministries of Health for both countries.

The study will be conducted in Dar es Salaam and Coastal Region aim to develop and evaluate a model of integrated HIV and NCDs care that could be both sustainable and effective. Project is funded by National Institute for Health Research – United Kingdom.

Director General of the National Institute for Medical Research advertise the Study Coordinator and Clinical Research Nurse which are required to be filled with highly motivated and competent Tanzanians on contract basis.

SCOPE OF WORK:

The overarching objective of the assignment is to provide operational and technical support to the study coordinator and Principal Investigator (Pi) to ensure efficient planning, programming, and monitoring of project activities. NIMR now invites applications from suitable, qualified and experienced persons to fill the following available vacancies.

1. ASSISTANT STUDY COORDINATOR (1 POST)

JOB DESCRIPTION

The assistant study coordinator will assist the project coordinator in supports, facilitates and coordinates the daily project activities and plays a critical role in the conduct of the study. By performing these duties, the assistant coordinator works with the project coordinator, PI, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study and.

RESPONSIBILITIES:

1. As assistant study Coordinator, ensures assigned study is conducted in accordance with

the National IRB regulation and Good Clinical Practices (GCP) guidelines:

2. Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities

3. Develops accurate source materials and ensures compliance from site staff

4. Provides accurate and timely data collection, documentation, entry, and reporting in both sponsor and study databases

5. Ensures appropriate credentialing and training of the entire study team

6. Supports the regulatory staff in the maintenance of regulatory documents in accordance with Study SOP and applicable regulations

7. Interfaces with research participants, to support efforts to determine eligibility and consenting of study participants according to protocol

8. Communicates and collaborates specific study requirements to the research team,

including internal and external parties, sponsor, monitors, PI, and study participants

9. Ensures compliance with research protocols, by providing ongoing quality control

audits, including maintaining ongoing investigational drug accountability

10. Disburses investigational drug and provides patient teaching regarding administration,

as necessary

11. Communicates and collaborates w/ study team including internal and external parties,

sponsors, PI, and study participants

12. Facilitating communication of patients’ progress to NIMR and MoHCDGEC on

implementation strategies; this include, provide regular status updates and progress reports to project management.

13. Facilitate timely and effective stake holders’ communication through regular meetings,

reporting, site visits and conference calls.

14. Manage effective relationships and open communication with project site facilities and

key stakeholders.

15. Compile and maintain all project documentation in accordance with Project SOPs and

procedures. Prepare quarterly, annual and terminal progress reports of the work done as well as scientific report.

16. To help study coordinator organize meetings, as necessary, with study team members

and collaborators, including programme, accommodation, travel, venues and social events

17. And carry out any other related duties as may be assigned

18. Day to day running of clinical trial

19. Screening, enrolment and randomisation of study patients

20. Day to day clinical management of patients & OPD management of patients after discharge

EDUCATION QUALIFICATION AND ESSENTIAL SKILLS

1. Bachelor of Medicine (MD) or equivalent knowledge

2. Experience to work with research organization.

3. Analytical skills ability, to understand complex subjects, extract and communicate relevant information from data and documents.

4. Ability to prepare comprehensive project documentation and reporting, using MS Office software, for internal and stake holders’ communication.

5. Project management skills, including a demonstrated ability to define scope, manage stakeholders, manage schedule/task activity, manage change and communicate risks.

6. Communication skills fluent written and spoken English and Swahili including presentation skills

7. Previous experience in the field of clinical trials, and knowledge of good clinical practice would be highly desirable;

8. Self-motivated; able to work independently to complete tasks and respond to department requests and to collaborate with others to utilize their resources and knowledge to identify quality solutions.

9. Strong ability to prioritize tasks for both self and team to meet requirements and deadlines

DURATION OF CONTRACT:

One-year contract which may be renewed on the basis of performance and mutual agreement.

COMPENSATION:

A competitive salary will be awarded to a successful candidate.

2. CLINICAL RESEARCH NURSE (5 POSTS)

JOB DESCRIPTION

The Clinical Research Nurse, under the guidance and supervision of the Project coordinator & Principal Investigator (PI), ensures the integrity and quality of clinical trials are maintained and conducted in accordance with GCP and local regulations, Institutional Review Board (IRB) approvals, and procedures. This position is primarily responsible for the accurate completion of visit procedures and collection of information from study patients according to protocols, and for protecting the health, safety, and welfare of research participants.

RESPONSIBILITIES:

1. Providing nursing care to research study patients:

2. Ensures compliance with each study’s protocol by providing thorough review and documentation at each subject study visit

3. Participates in recruitment and selection of study participants by interviewing and

documenting medical history to determine compliance with eligibility requirements

4. Performs medical tests, including, but not limited to, vital signs

5. Provides patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment

6. Documents medical data in patient chart to capture protocol requirements

7. Interfaces with research participants, to support efforts to determine eligibility and consenting of study participants according to protocol

8. Obtaining informed patient consent from patient or family member

9. Filing of consent forms

10. Establishing and maintaining a positive relationship with study patients

11. Chasing outstanding blood results (in conjunction with study doctors) and informing

study doctor of results

12. Documentation of relevant clinical information in patient records

13. Organizing follow-up care on patient discharge

14. Book and chase results of investigations (Chemistries, viral load )

15. Tracing non-attenders through note entries, phone calls, text messages or visiting them in the community

16. NCDs & HIV (ARV) counselling of study patients and their treatment supporters

17. Faxing CRFs using Datafax

18. Responding to error reports from Datafax in collaboration with the study doctor

19. Updating of patient follow-up spreadsheet

20. Liaising with laboratory staff on a daily basis regarding new positive results

21. Assist with study and sub-study specimen collection, storage and shipping as required

22. Positive relationship building with all hospital staff.

EDUCATION QUALIFICATION AND ESSENTIAL SKILLS

1. Diploma of Nursing from an accredited nursing school

2. A valid registration from reputable Board of Nurses

3. Two (2) years of recent clinical nursing experience in a hospital, clinic or similar health

care setting.

4. Nursing competency skills per scope of practice (i.e., performing vital signs, nursing assessments, etc.)

5. Ability to proactively identify and solve problems; demonstrated initiative is imperative

6. Must have communication skills with the public as well as physicians and co-workers

7. Ability to work independently as well as in team environment

8. Strong interpersonal, customer service and multi-tasking skills

9. Must be proficient in Microsoft Office Word and Excel, electronic health systems and

databases used in research environment

10. Ability to work under pressure, multi-task, and manage deadlines

DURATION OF CONTRACT:

One-year contract which may be renewed on the basis of performance and mutual agreement.

COMPENSATION

A competitive salary will be awarded to a successful candidate.

3. STUDY CLERK (5 POSITIONS)

Ensure complete, accurate and timely data collection through efficient use of resources and tools, observing the welfare of participants

RESPONSIBILITIES:

The post holder will be responsible for accomplishing the following

1. Ensure that all clients/ study participants who come to the clinic are registered

2. Ensure that all study documents are kept following study procedures in a confidential place.

3. Ensure that all study participants are given appointments and study registers are completed before the participants leave the clinic.

4. Ensure that case reporting forms are retrieved and help to locate missing forms and in a timely manner

5. Ensure that they maintain restricted access to the registry and always keep it under lock

and key.

6. Ensure proper accountability of project resources including participant reimbursements in line with NIMR policies

EDUCATION QUALIFICATION AND ESSENTIAL SKILLS

Certificate in nursing/record keeping or a relevant field.

2 years’ working experience on medical/health Organization

Keeping clinical trial/observational study participant records

computer skills including internet and emailing

DURATION OF CONTRACT:

One-year contract which may be renewed on the basis of performance and mutual agreement.

COMPENSATION:

A competitive salary will be awarded to a successful candidate.

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 30th July, 2018 to the address below. Applicants are also reminded to indicate all contact information necessary with which information can reach them easily. Apply Online Through

e-mail: muhimbili@nimr.or.tz and career@nimr.or.tz

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 & career@nimr.or.tzOnly shortlisted applicants will be notified. In case you do not hear from us in two weeks’ time after the closing date consider yourself unsuccessful.