Medical Writer 2

Medical Writing is organised as a global group of around approximately 100+ Medical Writing staff in US / Brazil, India, Europe, South Africa, Ghana, Japan, China / Taiwan, Australia, New Zealand.

The group mostly prepares study protocols and clinical study reports for Phase I-III interventional studies.

These cover an extremely wide range of indications, with oncology being one of the most common.

We also occasionally work on other documents (IBs, manuscripts, CTD summaries).

This role is home based and can be based anywhere in Australia.

Essential Functions

Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.

Manage day-to-day workload : identify project needs, track timelines and implement customer requests, keeping manager / senior staff abreast of progress on tasks and any potential problems with project work.

Lead customer meetings independently.

May give presentation to an existing customer (e.g. to discuss templates, results, lessons learned), responding appropriately to feedback.

May deliver basic level training to small groups or individuals within IQVIA on the role of the medical writer, on medical writing processes, or on specific customer templates / processes.

May also provide guidance to more junior colleagues.

May take the role of Project Manager for a small and short Medical Writing project.

Complete project finance activities, including monitoring and forecasting budgeted hours.

Understand budgets and project finance principles.

Interact with Project Leader / Project Finance Manager directly regarding straightforward financial issues, increasing ability to estimate hours needed for more straightforward / routine tasks.

May propose revisions to standard operating procedures (SOPs) or suggest process improvements for consideration.

Qualifications

Minimum Bachelor's Degree in life sciences related discipline or related field

At least 3 years of experience in medical writing or relevant.

Proficiency in Japanese is a bonus.

Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.

Ability to identify deficiencies, errors, and inconsistencies in a protocol or report.

Good understanding of common statistical methods used in clinical trials and / or interpretation of their results.

Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output.

Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.

Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues.

In depth knowledge of drug development, medical writing, and associated regulations.

Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.

Excellent written and oral communication skills including grammatical and technical writing skills.

Excellent attention to detail and accuracy.

Communicates clearly, effectively and confidently with others.

Demonstrated abilities in collaboration with others and independent thought.

Demonstrates confidence and maturity in most routine medical writing situations.

Demonstrates good judgement in requesting input from senior staff.

Ability to establish and maintain effective working relationships with coworkers, managers and customers.

Ability to effectively manage multiple tasks and projects.

Ability to proactively identify potential issues / risks, consider solutions, and raise with the customer, with senior guidance and input.

Must be computer literate.

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