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Seats For Sale2nd Hand, still in good condition, offroad seats for sale.Available for:YZ,YZF ,CRF, RMZ,KXPlease note they are mostly on the older models and not newer models.Please contact us for information and prices on0734835830.
2d
3
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CLUTCHES FOR OFFROAD BIKES FOR SALEWe have the following 2nd hand clutches for sale: 1.CRF 250 R2.CRF 450 R CORE3.CRF 450 R EXPPlease contact us for details and prices on 0734835830.
2d
12
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BIKE PARTS FOR OFFROAD/ATV/MX FOR SALE.We have a variety of different 2nd hand spares for sale:Plastics, body parts, electric parts, suspension parts, engine parts, gearbox parts and many more.Mainly on the following off-roadsYZ,YZF,CR,CRF,KX,KXF,RM,RMZ,XR and some Quad BikesWe have 2nd hand and new parts available.Please contact us for more details on 073 483 5830.
2d
8
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CRANKSHAFTS FOR OFFROAD/MX/ATV FOR SALE2nd Hand & Rebuilt Crankshafts for sale:Big variety available. Raptor 660 & 700YZ,YZF,YFZXR,CRFRMKXFBOMBARDIER Please contact us for more information and prices on 073 483 5830.
2d
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3d
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1mo
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23d
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1mo
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1mo
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Main purpose of the job:
To provide best practice data collection, clinical assessments, collection of specimens, and care, according to protocols, and to provide pre-and post-test HIV counseling
Location:
Wits RHI – C/O Esselen and Klein Street Hillbrow - Johannesburg
Key performance areas:
Inform participants about the studyObtain informed consent according to SOPs and screen potential participantsDraw blood from participants, process samples as required, and send samples or specimens to the laboratoryObtain vital signs and conduct special investigations e.g., ECG, Rapids, etc.Administer study questionnaires/interviewsInform participants of test results, as requiredProvide appropriate health education and counseling where necessaryRefer participants to alternative care if necessaryTake responsibility for the Emergency Contact Research cell phone, during the delegated time periodTaking of the minutes for weekly research team meetingsEnsure labs are printed, converted, graded, and reviewed by an investigator prior to CRF completion, according to SOPsCollect participant data from medical notes and complete CRFsMaintain full clinical records for all participantsMaintain an inventory of laboratory samplesPerform sample-related activities such as but not limited to labeling, storage, collection, and completion of DCFsCompile relevant reports and feedback on all activitiesQuality control CRFs and other study documentsTake ownership and accountability for tasks and demonstrates effective self-managementFollow through to ensure that quality and productivity standards of own work are consistently and accurately maintainedMaintain a positive attitude and respond openly to feedbackTake ownership of driving your own career development by attending training and development sessions and relevant meetings
Required minimum education and training:
Diploma in General Nursing (3 years)A valid driver’s license
Required minimum work experience:
Minimum 1 year of nursing experience in HIV
Desirable additional education, work experience, and personal abilities:
A diploma in Primary Health Care or similar will be an advantageCertification in good clinical practiceExperience in a research environmentExperience in pediatricsOrdered and systematic with strict compliance to protocolsBe tactful, respectful, and maintain confidentialityGood administrative skills together with working knowledg...
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly93d3cuZGl0dG8uam9icy9qb2IvZ3VtdHJlZS8xOTgwMDg0MDkxP3NvdXJjZT1ndW10cmVl&jid=1267442&xid=1980084091
2y
5
2mo
5
1mo
7
11d
5
R 78,000
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Yamaha YZ450F 23Hours on since new
bike is in immaculate condition
new on bike
D.I.D MX gold series chain
PBR sprockets
Dunlop MX33 tyres
Excel Takasago rims
plastics
ODIgrips
graphics
shock, forks and motor just been serviced
Motocross
Mx
Dirt Bike
yamaha
ktm
Husqvarna
honda
kawasaki
Suzuki
125, 250, 450
yz, yzf, Cr, Crf, kx, kxf, Fc, Tc, Rm, Rmz, Sx, Sxf
18d
1
Main purpose of the job: To perform on-site laboratory processes and ensure efficient workflow of the onsite laboratoryLocation: Wits RHI – 7 Esselen Street, Hillbrow, Research Centre - Johannesburg On the 3rd and 4th Floor Key performance areas: Perform and document all lab testing as per GCLP, SOPs, and Protocol requirements under the supervision of a medical technologistCo-ordinate all daily lab activities to ensure work is completed within the required turnaround time (TAT)Ship samples to outsourced laboratoriesFollow up on DCF and Final reports within TATDistribute laboratory results to doctors nurses/site coordinators effectively and timeouslyPerform all in-house storage using the LDMS system if requiredPerform laboratory equipment maintenance, lab decontamination, and temperature surveillance in the onsite laboratoryPerform backup duties at other Wits RHI on-site labs when requested to do soPerform troubleshooting activities as and when required and ensure communication with the lab manager/supervisor Medical TechnologistEnsure equipment maintenance is performed as per maintenance schedules and SOPsMonitor and control stock levels and ensure sufficient stock is available such that lab activities are not adversely affectedTimeous and logical filing of all laboratory recordsDemonstrate cost consciousness, and assist in meeting budgetary targetsRepresent the on-site Laboratory in meetings as required by managementCommunicate with the study team, suppliers, lab manager, or other stakeholders in a professional and effective mannerComply with Good Clinical Practice (GCP), Protocol requirements, and Standard Operating Procedures (SOPs) in all lab duties, processes/activitiesVerify the accuracy of data in source documentation and accuracy of transcription from source data to Case Report Forms (CRF) as neededEnsure errors on source documents e.g. CRF are corrected, initialed, and datedSupport the timely transmission/data faxing of relevant Case Report Forms following QC activity (as needed)Ensure completion of corrective action of internal and external QC reports and monitoring reviewsPerform Quality control procedures as lab SOPS and LQMPEffectively communicate/report all quality challenges to the lab managerEnsure conformance to the External Quality Assurance programIdentify and communicate trends in the quality of lab testing or control proceduresAttend to audit reports and effectively implement corrective action and future preventative measuresAssist with the development of new lab documentsEnsure lab documentation filing is up to date and audit-ready throughout the studyPrepare lab reports as requested eg monthly reports, lab closeout reports, audit closeout reports, etc.Required minimum education and training: Technicians Certificate in Medical Technology Health Professions Council of South Africa
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA4XzYyNjE3X180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1220680&xid=1108_62617
2y
1
The main purpose of the job: To administer, maintain and coordinate the logistical aspect of clinical trials according to Good Clinical Practice, study Protocol and Standard Operating Procedures, and act as a pivotal point of contact for the clinical trial team and the sponsorLocation: Helen Joseph Hospital, JohannesburgKey performance areas: Assist in the Recruitment, Screening, and Enrolment of eligible participants according to Protocol requirements.Assisting in the recruitment and consenting and enrolment of study participantsAssist the Medical Officers/Principal Investigator, and Study team in the day-to-day running of the studyManage scheduled and unscheduled patient visits and appointments in accordance with the study protocolConduct protocol and SOP training for staffLiaise with the CHRU regulatory department for the reporting of SAEs and protocol deviations etc.Liaise with the Sponsor, Laboratory, Pharmacy, and external monitoring contractorPerform participant’s vitals (as and when required) and direct patients to relevant assessment.Assist with study specimen collection (i.e. blood, urine, sputum, cervical specimens, and semen).Collect, process, and ship specimens as per protocol.Administering trial medications and diagnostic tests if requiredCompletion of Source Documentation and e-CRF’s within strict timelinesComplete relevant research questionnaires, assessments, CRF transcription.Review of participant files for completenessMaintain and update the Investigator Site FileSite supervision and managementManagement of freezers/fridges for samples kept at the siteRequired minimum education and training: Qualified as a Professional Nurse Professional body registration: Registered with the South African Nursing Council (SANC) Required minimum work experience: 3 years of experience in a clinical research environmentDesirable additional education, work experience, and personal abilities: Ability to lead and work independently as well as be part of a multidisciplinary teamFlexibility to adapt to changes in study requirementsAbility to speak local languagesComputer LiteracyGCP Certification is advantageousStaff supervisory and management experienceAble to exercise discretion and independent decision makingEmpathy and UnderstandingDriver’s License and own vehicleTO APPLY: Only if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.Please Apply Online and complete your registration on Ditto Hire (our application tracking system) to enable and protect you as a candidate 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. A
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA5Xzg5OTAyX180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1223424&xid=1109_89902
2y
1
Main purpose of the job: To administer, maintain and coordinate the logistical aspect of clinical trials according to Good Clinical Practice, study Protocol and Standard Operating Procedures, and to act as a pivotal point of contact for the clinical trial team and the sponsorLocation: Helen Joseph Hospital, JohannesburgKey performance areas: Assist in the Recruitment, Screening, and Enrolment of eligible participants according to Protocol requirements.Assisting in the recruitment and consenting and enrolment of study participantsAssist the Medical Officers/Principal Investigator, and Study team in the day-to-day running of the studyManage scheduled and unscheduled patient visits and appointments in accordance with the study protocolConduct protocol and SOP training for staffLiaise with the CHRU regulatory department for the reporting of SAEs and protocol deviations etc.Liaise with the Sponsor, Laboratory, Pharmacy, and external monitoring contractorPerform participant’s vitals (as and when required) and direct patients to relevant assessment.Assist with study specimen collection (i.e. blood, urine, sputum, cervical specimens, and semen).Collect, process, and ship specimens as per protocol.Administering trial medications and diagnostic tests if requiredCompletion of Source Documentation and e-CRF’s within strict timelinesComplete relevant research questionnaires, assessments, CRF transcription.Review of participant files for completenessMaintain and update the Investigator Site FileSite supervision and managementManagement of freezers/fridge for samples kept at the siteRequired minimum education and training: Qualified as a Professional Nurse Professional body registration: Registered with the South African Nursing Council (SANC) Required minimum work experience: 3 years experience in a clinical research environmentDesirable additional education, work experience, and personal abilities: Ability to lead and work independently as well as be part of a multidisciplinary teamFlexibility to adapt to changes in study requirementsAbility to speak local languagesComputer LiteracyGCP Certification is advantageousStaff supervisory and management experienceAble to exercise discretion and independent decision makingEmpathy and UnderstandingDriver’s License and own vehicleTO APPLY: Only if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.Please Apply Online and complete your registration on Ditto Hire (our application tracking system) to enable and protect you as a candidate 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. AJ Per
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA5Xzc2OTYzX180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1197352&xid=1109_76963
2y
5
23d
4
25d
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2mo
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