Clinical Research Associate
Job Description
Central Monitor position
Exciting oppurtunity to join our South African team as a central monitor. Use your good analytical skills and keen eye to identify data discrepancies and trends.
Your tasks and responsibilities
Direct, motivate and manage the activities of the clinical trial sites to ensure that data and information is completed in the eCRF is accurately and timely.
Review the eCRF for errors and identify trends.
Use your remote monitoring experience to assist with the set-up and writing of 'Remote monitoring SOPs'
Monitor uploaded source documents remotely
Interact with site teams telephonically / via email
Your qualifications
Life-science degree or equivalent experience
At least 5 year’s field experience as a CRA
Flexible, easy going with excellent people skills
Responsible, highly motivated team player who can communicate within a team and are confident with investigators and Sponsor
What we have to offer you
Growth potential in a highly specialised, innovation oriented team, working closely to science flexible working hours
A growing international team with a far more than average company loyalty
All the advantages in daily business, a smaller, owner-managed and specialised CRO brings along
A really warm welcoming team where personality and qualification is clearly rated as more important than your academic title.
No travel, office based position
Skills Required
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Job Detail
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Job IdJD459008
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IndustryPharma/Biotech/Clinical Research
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Total Positions1
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Job Type:Full Time
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Salary:Depends
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Employment StatusPermanent
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Job LocationCape Town, South Africa
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EducationAny Graduate
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Experience3 - Years
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Apply ByFeb 20, 2020
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Job Posting DateJan 20, 2020