To manage and lead the clinical trial team and activities and to provide health care to patients participating in clinical trials according to study protocols
Location:
Parktown xe2x80x93 Johannesburg
Key performance areas:
Clinical Trial Management
Compile source notes and recruitment tools
Undertake recruitment of eligible patients according to protocol requirements
Actively engages with sponsors and attends project meetings, as and when required
Plan, implement, and complete the clinical research activities for clinical trials
Conduct clinical trials in accordance with GCP regulations and Standard Operating Procedures (SOP)
Proactively resolve protocol queries and missing data with Study Coordinators and/or Clinical Trials Assistants
Patient care and screening
Screen and enroll patients in accordance with the study protocol and ethical guidelines
Provide medical care to patients
Review patient vitals, echocardiograms, scans, and other study-related results.
Report any adverse events.
Study the full history of referred patients from other clinics and discusses the relevant risk factors
Quality Assurance
Perform spot-check evaluations to quality control clinical source notes and CRFs
Conduct regular clinical team meetings to identify, discuss and solve study queries
Meet with Monitors as and when required
Teamwork & Support
Conduct staff training i.e. CRF completion training, quality assurance, and other study-related training
Assist the team with ad hoc assignments and duties
Required minimum education and training:
MBBCh/MBChB Degree
Certification in Good Clinical Practice (GCP), project management, and a license in drug dispensing will be an advantage
Required minimum work experience:
Minimum one (1) year of experience in clinical trials
Professional body registration:
Registration with HPCSA
Desirable additional education, work experience, and personal abilities:
Displays serious concern for the safety and well-being of patients
Ability to function and operate strategically with sound clinical and business acumen
Confidentiality, tact, and discretion must be maintained at all times
Thorough, with good attention to detail
Ordered and systematic in approach to tasks, with strict adherence to protocol
Exceptional planning and organizational skills are required together with working knowledge of Microsoft Office
Able to exercise discretion and independent decision-making
Ability to prioritize own workload, take initiative (pro-active) and work to tight deadlines
Self-motivated with high regard for work ethic, values, and integrity
Overtime and traveling may be required from time to time
Communicate effectively with patients, management, clinicians, and sponsors
Work as part of the multidisciplinary team to ensure good patient care and good-quality data
Work effectively, co-operatively, and amicably with patients and staff
TO 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.
Please take note that the applicants who do not adhere to the above criteria will not be considered for the respective position.
The closing date for all applications: 29 August 2023.
Note AJ Personnel is fully POPI compliant.
Note WHC, in accordance with their 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.
Please note:
AJ PERSONNEL is only responsible for the advertising of the advertisement on behalf of their client Wits Health Consortium.
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.
AJ Personnel does not have any salary or other information regarding the position.