Category

Description

About the role:

Prepare, organise, conduct and follow-up routine monitoring and close out visits as per relevant study plan
Motivate and train investigators and site staff to ensure obligations in regards to study timelines
Ensure ethics submissions are made by investigator sites in a timely manner
Adherence to ICH-GCP and any other regulatory guidelines and requirements including adverse events and serious adverse event reporting
Compliance with mandatory SOPs as agreed for the study
Complete all reports accurately and within the predetermined timelines.

About you:

At least 2 years experience in a similar role within a CRO or Pharmaceutical company
Excellent co-ordination and time management capabilities including the ability to prioritise demands
Tertiary qualifications in Science or a relevant area preferred
Strong interpersonal skills including the ability to communicate well with various types of people
Excellent verbal and written communication skills
Proficiency in the use of the Microsoft Office suite of products.

We are searching for individuals who are results oriented and able to handle rapidly changing priorities in a fast moving environment. You must be willing to extend yourself, take on new challenges with a

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