Lead Nonclinical Medical Writer
About the job
Acumen was established by industry-experienced medical writers and clinicians with the vision of creating a world leading medical writing company that places writers at the forefront. Our primary objective is to cultivate a supportive and collaborative environment where writers can thrive and deliver exceptional work. With a track record of serving over 100 Sponsors in the pharmaceutical and biotechnology industry, our medical writing teams make significant contributions to drug regulatory submissions (INDs, CTAs, NDAs, and BLAs) and publications across diverse therapeutic areas.
Acumen is currently seeking a highly skilled Senior/Lead Nonclinical Writer to join our growing team as a remote writer on a permanent basis. In this position, you will directly interact with Sponsors to author and oversee a wide range of nonclinical regulatory documents. Lead Nonclinical Writers work as individual contributors or medical writing team leaders, with the support of Acumen quality control, project management, and software development professionals. For the ideal candidate, this role may expand to include management and training of junior nonclinical writers.
Acumen is committed to supporting and training well-rounded clinical developers. Ours is a culture of sharing knowledge and expertise and providing opportunities for cross-functional training within the medical writing landscape. To attract and retain the very best talent, we offer a compensation package that is among the most competitive in the industry:
Generous benefits package included (health and dental and vision insurance, profit share, 401K match)
Salary is $120,000 and up, depending on experience
Full-time, remote position
US residents only
Qualifications
A minimum of 3 to 5 years of experience in the field, with a strong track record in nonclinical document writing, including Module 2 eCTD summaries, pre-IND briefing documents, and nonclinical study reports
An advanced scientific degree, preferably a PhD, in the biological sciences
Ability to work collaboratively in a fast-paced, dynamic environment is essential
Strong attention to detail and excellent written and verbal communication skills
In-depth knowledge of regulatory requirements, guidelines, and standards
Proficiency in Microsoft Word and other relevant software tools
Strong leadership and team management skills, including mentoring junior medical writers
Knowledge of therapeutic areas relevant to our portfolio (including oncology and immunology) is desirable
Interested? Send us a resume and a brief cover letter. We look forward to hearing from you!
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