Medical Writer **Associate Director **Lead a team in Regulatory and Clinical Writing for Rare Genetic Diseases **Fully Remote

Reference: JPC570

Expiry Date: 01-08-2023

Category Regulatory Affairs

Salary: Competitive

Job Type: Full Time

Middlesex County
United States

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Job Description

Are you an experienced medical writer eager to develop your team-managing skills?

Are you knowledgeable in both clinical and regulatory writing?

Do you have strong interpersonal skills and excellent writing skills?

If so, then you could be the new Lead Medical Writer our client is looking for!

This smaller biotech is looking for a detail-oriented Lead Medical Writer to join their midst. My team and I are helping our client find someone who can comply with industry style guidelines and work well in a team within condensed timelines.

About the role:

- It will allow you lead the narrative and be responsible for alignment of content across key regulatory documents and recommending improvements to the documentation preparation processes and templates

- It will put your name to maintaining compliant standard operating procedures and maintenance of medical and regulatory writing deliverables

- It will give you the voice to shape and contribute to program goals, key messages and timeline discussions

- It reports to a highly accomplished VP, who will support you in developing and growing the medical writing function

- It comes at an Associate Director level, with enough room and support to help you grow at your own speed

- It is fully remote and comes with an impressive salary, solid bonus, stock and benefits.

About the company:

- It’s a smaller company (about 300 people), where everyone is committed to the work they are doing, the science behind it, the difference they are making for their patients and the support they can offer to their colleagues

- The company culture is very friendly, caring and engaging and it will not take the right person long to be completely immersed in it

- The executive team is comprised of experienced professionals in all sectors, who all have proven track records on either discovering, developing, or commercializing drugs in their therapy areas

- The pipeline is very focused, the market cap - solid, and the team has great readout on the products in development

- They have their own scalable, in-house GMP manufacturing capabilities, which allows them to move to clinical phase much more readily

- They have stable collaborations with several leading global pharma organizations, for long-term co-development and co-commercialization for several NMEs.

To Apply!

If you are interested in hearing more about this or other roles in Medical Writing, please contact me, Theo Moore on 587.216.9302 or via email, or my colleague Ivan Nash on +1-908-378-8980.