Job Description

Research Medical Officer (Doctor-12 Months FTC) - JhbAdditional Information:The Mycology Division aims to improve the outcomes of people affected by serious, life- threatening fungal diseases in South Africa and the African region through public health-focused epidemiological, clinical and basic science research and innovationTheir work also stretches to other important infectious diseasesMain Puprose of the Job:To join the COMBAT Candida clinical study site team at Chris Hani Baragwanath Hospital and manage day-to-day activities of the study site, under direct supervision of the site principal investigator(s) and the study clinical lead/co-ordinator, according to the study protocolTo contribute to the data analysis and any peer-reviewed publications arising from the study, and to contribute to related sub-studies or projectsLocation:Chris Hani Baragwanath Academic Hospital (main site) & Helen Joseph Hospital - JohannesburgKey performance areas:Contribute to the development of study documentation including protocols, patient information sheets and consent forms, SOPs/WPDs, quality assurance and quality control guidelines and training manualsCompile source notes and recruitment toolsParticipate in regular meetings between the clinical teams at the sites and ensure good communications between sites and the management groupMaintain close contact with the study management group and consult them on strategic issues that might have any safety or major financial implications for the project. This will include, but not be limited to, collation of weekly reports of study progress to be shared with the study management groupConduct clinical study in accordance with GCP regulations and standard operating proceduresProactively resolve protocol queries and missing data with the study Management GroupCover duties of the COMBAT trial study team during staff leave periodsAssist in all clinical aspects of the study, including venepuncture, cannulation, blood sample processing, drug administration and clinical observation when necessaryOversee clinical procedures including dispensing of related drugs to study participants and other protocol related procedures, with the study nurses and pharmacistsScreen and enroll patients in accordance with the study protocol and ethical guidelinesObtain participant's informed consent before commencement of any study related activitiesConduct any pre-study entry medical evaluation for potential participants & offer daily clinical care to study participants, with the study doctor. S/he should also ensure that patients who need referral to other health care services are duly referredMaintain confidentiality of all participants' study informationReview patient vitals, X-rays, echocardiograms, scans and other study-related resultsReport any adverse events and ensuring appropriate action is taken until a final report is completedStudy the full history of referred patients from other clinics and discuss the relevant risk factorsMonitor and evaluate the quality of care and counselling conducted at the study site(s) and assess findings with the teamPerform spot check evaluations to quality control clinical source notes and CRFsMonitor the Study Recruitment/Retention Plan including planning meetings to address challenges of study enrolment and participant retentionPlay a supervisory role for the study clinical and nursing teams to ensure that; teams adhere to the set standard operating procedures in the conduct of clinical trials and that all staff are full trained in the SOPs pertaining to their daily work; data collection process is enhanced for quality with quality control measures in place; recruitment/accrual targets are being met; proper source documentation procedures are followedManage the duties of the clinical study site teamIdentify study specific training needs and consequent provision of training in liaison with the Trial Ops Manager for study staff during study implementationConduct staff training i.e. CRF completion training, quality assurance and other study related trainingTo act as a leader, resource and role modelPerforms any other duties as assigned by the Site PI, Senior Research Clinician and/ or CIRequired minimum education and training:MBBCh DegreeHPCSA RegistrationCertification in Good Clinical Practice (GCP)Project management qualification will be an advantageRequired minimum work experience:Minimum 1-year work experience, preferably in a Clinical Research environmentDesirable additional education, work experience and personal abilities:Displays serious concern for the safety and well-being of patientsAbility to function and operate strategically with sound clinical acumenConfidentiality, tact and discretion must be always maintainedThorough, with good attention to detailOrdered and systematic in approach to tasks, with strict adherence to protocolExceptional planning and organizational skills are required together with working knowledge of Microsoft Office and EmailAble to exercise discretion and independent decision-makingAbility to prioritize own workload, take initiative (pro-active) and work to tight deadlinesSelf-motivated with a high regard for work ethic, values and integrityTO APPLY:Only if you meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.Please Apply Online and complete your registration via our website to enable and protect you as a candidate, and to accept the new POPIA terms and conditions.This will then create your permanent profile with which you can apply for all jobs as advertised by AJ PERSONNEL.However, you may remove your profile from AJ PERSONNEL when you are no longer in the job market.Please take note that the applicants who do not adhere to the above criteria will not be considered for the respective position.Wits Health Consortium will only respond to shortlisted candidates.Candidates who have not been contacted within two weeks of the closing date can consider their applications to be unsuccessful.Closing date: 03 March 2025Note: No CV will be accepted after the closing date.Please note:WHC, in accordance with its Employment Equity goals and plan, will give preference to suitable applicants from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments thereto.AJ Personnel is only responsible for advertising and the response handling on behalf of their client Wits Health Consortium.AJ Personnel does not have any salary or other information regarding the position.For more information please contact:Amanda Celliers

Skills Required