Study Supervisor
1 week ago
**Summary**
Responsible for the supervision of Clinical Staff for their assigned studies, organisation of study documentation and execution of study protocols in Clinical Research Environment under the direction of the Principal Investigator and or the Site Manager/ Site Director.
The Study Supervisor will report directly to the Site Director & Site Manager giving weekly updates on their assigned studies, apprising them of any issues, seeking guidance when necessary and completing assigned tasks with mínimal supervision.
**1.0 - Key Requirements**
- Good written and verbal communication skills
- Ability to understand medical/scientific terminology relative to study type
- Good inter-personal skills
- Good team player
- Ability to convey information in a clear and concise manner
- Ability to follow protocols
- Ability to lead a team in a chosen direction
- Ability to maintain accurate records, either electronically or as hard copies
- Ability to supervise multiple studies
- Ability to allocate resources
- Ability to train other personnel in study related issues
**2.0 - Education and experience**
A good standard of education preferable to degree level.
Experience conducting clinical research.
Experience in training personnel.
Able to conduct: informed consent, interview, assessment study of eligibility requirements, instrumentation, needed study procedures.
**Job Types**: Full-time, Permanent
Pay: $40,000.00-$43,000.00 per year
**Benefits**:
- Dental care
- Extended health care
- Paid time off
- Vision care
Schedule:
- 8 hour shift
**Education**:
- Bachelor's Degree (preferred)
**Experience**:
- Clinical laboratory: 2 years (preferred)
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