• The Clinical Contracts Specialist (CC Specialist) is responsible for the timely development of investigator grants and Clinical Trial Agreement templates during the start-up stage of a Clinical Trial. The CC Specialist will work closely with Project Management, Clinical Operations, Legal teams, and the client to ensure finalisation of approved site budgets and execution of approved site Clinical Trial Agreements. The ideal candidate will be professional, analytical and possess excellent written and verbal communication skills
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Minimum Qualifications & Experience:

• * Bachelor’s Degree in a relevant field (science, law or other).
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• * Minimum 3 years’ experience in the clinical trials industry including experience in contract and budget negotiation.
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• * Understanding of business/financial concepts used in clinical trials.
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• *Excellent communication and interpersonal skills. Good organisational skills; positive team player; attention to detail.