| Title | Senior Clinical Research Associate |
| Description | Performs and coordinates all aspects of the clinical monitoring process in accordance with ICH GCP and FDA guidelines and global/local SOPs to assess the safety and efficacy of investigational products and/or medical devices.
Responsible for ensuring that data will pass international quality assurance audits.
Effective resource management and in ensuring time lines are met
Represents the company in the global medical research community and develops collaborative relationships with investigational sites.
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| Required Skills | Strong analytical and problem solving abilities
Result-oriented, attention for details and organized
Effective interpersonal and verbal/written communication skills
Able to travel as and when required
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| Qualification | Degree in Science with a major in Pharmacy, Biological Life Sciences or Nursing from a recognized Tertiary Institution.
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| Experience | Prior clinical monitoring experience in the capacity of a CRA (minimum 3 years) |
| Contact details | Please send updated resume (including salary information and notice period) to the suriati@resourcescientific.com, or call +65 6275 0183 for enquiries.
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