Medical Writer II / Senior Medical Writer (Adelaide)

Medical Writer II / Senior Medical Writer (Adelaide)

10 Oct
|
Avance Clinical
|
Adelaide

10 Oct

Avance Clinical

Adelaide

Medical Writer II / Senior Medical Writer

Australian based, regulatory Medical Writer II or Senior Medical Writer required.

Remote, Hybrid or Office based working are all options.

Who are we?

We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980's. If you already work in this industry, you'll know that we are experts in our field.

Why should you join Avance Clinical?

We have a great, employee centric culture and offer excellent long term career prospects. We believe in work / life balance and offer 100% working from home (WFH) and hybrid options. We've doubled in size this past two years and have promoted 25% of our people in the last 12 months.

You'll be joining a high performing, supportive, established team of experienced Medical Writers & Editors most of which have a PhD.

You'll work on a diverse range of therapeutic areas and get to really explore the science behind a project.

We're seeking people that thrive in a positive environment, who are inquisitive and keen to have a genuine opportunity to learn and grow in a business that is expanding.

Broad Purpose

You’ll be responsible for the coordination, writing and editing of Investigator Brochure's (IBs), Clinical Study Protocols (CSP), Participant Information and Consent Forms (PICFs), Clinical Study Reports (CSRs) and any other clinical study documents required as part of the medical writing (MW)



range of services. The role also serves as a primary MW technical contact for other Avance departments and the client, for any clinical study documents assigned to be prepared, as well as mentors Medical Writers on MW tasks and maintaining quality processes.

Qualifications, Skills and Experience

- Ordinary degree in a scientific or relevant discipline.
- Higher degree in scientific or relevant discipline (desirable).
- Minimum 2 years of experience as a MW with prior experience in preparation of IBs, CSPs, PICFs, CSRs or other clinical trial documents.
- Minimum 3 years of experience in the biotechnology / pharmaceutical / clinical research industry.
- Strong research report writing skills and/or demonstrated experience in writing peer reviewed journal articles.
- Knowledge of ICH GCP guideline, ICH guideline, medical terminology and clinical trials processes.
- Knowledge of statistics and data analysis and presentation methods (desirable).
- Knowledge of pharmacokinetics (desirable).
- Excellent time management and organisational skills.
- Mentoring/leadership experience.
- Excellent oral and written communications skills.
- Demonstrated initiative,



reliability and ability to work unsupervised.
- Willingness to work in, and be supportive of, a positive and agile team culture.
- Intermediate to advanced skills in MS Office suite.

What next?

As a growing business we're looking for likeminded people to join us – we hope that's you.

- You must have full Australian working rights to be considered

At Avance difference is encouraged, its celebrated and it's something we strive for. We empowercultural, disability, LGBTI+, and gender equality.

Medical Writer / Scientific Writer / Biotech / CRO / Pharmaceutical / Regulatory Writer / Clinical Research / Clinical Trials / Adelaide / Brisbane / Melbourne / Sydney / Perth / PhD / work from home / remote working

Unlock job insights

Hirer responsiveness Salary match Number of applicants

Avance Clinical is the largest specialist Australian and US CRO delivering quality clinical trials in Australia, New Zealand and North America for international biotechs.

The CRO has been delivering clinical drug development services for international biotechs for FDA and EMA regulatory approval, for more than three decades.

Avance Clinical is the largest specialist Australian and US CRO delivering quality clinical trials in Australia, New Zealand and North America for international biotechs.

The CRO has been delivering clinical drug development services for international biotechs for FDA and EMA regulatory approval, for more than three decades.

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📌 Medical Writer II / Senior Medical Writer (Adelaide)
🏢 Avance Clinical
📍 Adelaide

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