The Helse Nord Tuberculosis Initiative (HNTI) is a collaborative programme between the Kamuzu University of Health Sciences (KUHeS), Malawi-Liverpool-Wellcome Trust Clinical Research Programme (MLW), and Helse Nord RHF of the University of Tromsø in Norway. HNTI supports collaborative and multidisciplinary tuberculosis (TB) research within the KUHeS with the long-term goal of building local scientific research capacity that is sustainable, internationally excellent and that makes a direct contribution to local and international TB diagnostic capacity control policy and practice.

The Helse Nord Tuberculosis Initiative (HNTI) under the PanACEA (Pan-African Consortium for the Evaluation of Antituberculosis Antibiotics) consortium wishes to conduct a multiple arm, multiple stage (MAMS), phase 2B/C, open label, randomized, controlled platform trial to evaluate experimental arms including an increased dose of rifampicin, an optimized dose of pyrazinamide, moxifloxacin and sutezolid, in adult subjects with newly diagnosed, smear-positive pulmonary tuberculosis. The aim of the study is to assess the efficacy of new regimens for treatment of drug-sensitive tuberculosis (TB) disease.

The study wishes to engage two (2) research nurses and one (1) research clinical officer who would be required to work full-time   under the STEP 2C study to be stationed at Queens Elizabeth Central Hospital. Details of the positions are as follows;

RESEARCH NURSE – 2 POSITIONS

DUTIES AND RESPONSIBILITIES

• Assessing participant enrollment criteria and conducting informed consent
• Collecting biological samples from participants
• Documenting and maintaining accurate records of study participant visits and procedures
• Ensuring that study procedures and protocols are followed
• Coordinating and working closely with hospital staff and community leaders on study project activities
• Assisting with sample organization, storage, and transport
• Compiling clinical data and entering it into a database
• Collaborating with Ministry of Health staff, study monitors and other international collaborators

QUALIFICATIONS

• Bachelor of Science in Nursing or Bachelor of Science in Nursing and Midwifery

GENERAL ATTRIBUTES

The ideal candidate should have the following attributes:

• Excellent oral and written communication skills.
• Proficiency in using computers, particularly working with internet, emails and MS Office packages.
• Interested in clinical or public health research
• Good interpersonal skills and the ability to work in a team.
• Ability to consistently follow procedures and systems put in place.
• Good problem identification and solving skills.

RESEARCH CLINICAL OFFICER -1 POSITION

DUTIES AND RESPONSIBILITIES

• Screening potential study participants to ensure eligibility criteria are met

• Administering informed consent to eligible participants and ensuring they understand the study procedures.

• Administering study drugs and monitoring for adverse effects.

• Conducting regular physical exams and collecting biological samples for laboratory analysis.

• Documenting study data accurately and maintaining accurate study records.

• Collaborating with other members of the study team to ensure study protocols are followed.

• Monitoring and managing participants’ symptoms and managing any adverse events.

• Conducting follow-up visits with participants to monitor progress and collecting additional data.

• Maintaining confidentiality of study information and participant data.

• Participating in regular meetings and training sessions to stay informed on study updates and advancements

• Collaborating with Ministry of Health staff, study monitors and other international collaborators

QUALIFICATIONS

• Diploma in Clinical Medicine

• At least 2 years of experience working in a clinical trial setting; with experience in tuberculosis treatment preferred

• Valid medical license and certification as a clinical officer.

GENERAL ATTRIBUTES

The ideal candidate should have the following attributes:

• In-depth knowledge of TB treatment and clinical trial design, Good Clinical Practice (GCP) guidelines, and regulatory requirements.

• Excellent written and verbal communication skills, with the ability to effectively communicate with patients, physicians, and other members of the healthcare team.

• Strong attention to detail and accuracy, with the ability to maintain detailed and accurate patient records.

• Ability to identify and solve problems independently and as part of a team.

• Excellent time management skills and ability to work under tight deadlines.

• Strong interpersonal skills, with the ability to build positive relationships with patients, families, and healthcare team members.

• Proficiency in using clinical trial software and other computer systems and tools.

APPLICATION PROCEDURE

Suitably qualified candidates should submit their applications in one pdf file consisting of Application letter, copies of certificates, detailed Curriculum Vitae and names and contact details of three traceable referees. Applications should be submitted via email to  [email protected]  and  [email protected]  with the title of the job and name of the project on the subject line of the email. The Application letter should be addressed to:

The Registrar
Kamuzu University of Health Sciences
P/Bag 360
Chichiri
Blantyre 3

Applications should be received no later than 29th March 2023. Only short-listed candidates will be acknowledged