Clinical Trial Study Doctor - Johannesburg Verfied

Salary Negotiable Johannesburg, Gauteng Johannesburg, Gauteng more than 14 days ago 24-06-2016 8:59:32 AM
20-07-2016 9:00:17 AM
Main purpose of the job
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 and Baragwanath, Johannesburg

Key performance areas
Compile source notes.
Compile recruitment tools (if applicable).
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.
Proactively resolve protocol queries and missing data with Study Coordinators and/or Clinical Trials Assistants.
Screen and enroll patients in accordance with 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.
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.
Train staff on protocol requirements.

Required minimum education and training
MBchB or equivalent

Professional body registration
HPCSA registration

Required minimum work experience
Minimum 1 years’ experience in a clinical trial environment.
Prior exposure to an oncology environment is advantageous.

Desirable additional education, work experience and personal abilities
Certification in good clinical practice (GCP).
Communication skills both written and verbal.
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 work load, take initiative (pro-active) and work to tight deadlines.
Self-motivated with a high regard for work ethic, values and integrity.