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Principal Medical Writer - CRO / Melbourne
This job has expired or may no longer be taking applications, but other similar jobs are available.
Added: | 2022-12-02 |
Location: | Melbourne |
Salary: | Competitive salary (experience dependent) |
Duration: | Permanent |
Apjid | 3 |
Principal Medical Writer
We are seeking an experienced Medical Writer who will confidently lead medical writing projects across this dynamic and growing boutique CRO!
You will contribute to the business growth of medical writing services with your excellent business acumen as part of an established but growing mid-sized CRO.
You'll provide project leadership across all development, writing & editing of scientific, clinical content as, Investigator Brochures (IB), Clinical Trial Protocols, Participant Information Consent (PIC) and Clinical Study Reports, as well as ensuring medical accuracy & regulatory compliance across promotional tools. Developing SOPs, internal guidelines & best practice for content development.
An exciting opportunity to join a growing CRO with plenty of further career growth opportunities within as they continue to expand!
To be successful, you will have;
We are seeking an experienced Medical Writer who will confidently lead medical writing projects across this dynamic and growing boutique CRO!
You will contribute to the business growth of medical writing services with your excellent business acumen as part of an established but growing mid-sized CRO.
You'll provide project leadership across all development, writing & editing of scientific, clinical content as, Investigator Brochures (IB), Clinical Trial Protocols, Participant Information Consent (PIC) and Clinical Study Reports, as well as ensuring medical accuracy & regulatory compliance across promotional tools. Developing SOPs, internal guidelines & best practice for content development.
An exciting opportunity to join a growing CRO with plenty of further career growth opportunities within as they continue to expand!
To be successful, you will have;
- A positive 'can do' attitude
- Degree or equivalent combination of education, training & industry experience
- Experience writing regulatory documentation including study reports & protocols
- Thorough medical terminology knowledge & good understanding of clinical trial processes and ICH GCP guidelines
- Excellent verbal & written communicator
- Ideally experience in developing & delivering training programs within Medical Writing
- Good understanding of drug development & awareness of regulatory affairs
- Australian Citizen or Permanent resident
How to Apply
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