Associate Director Medical Content Review
Canopy Life Sciences LLC - Danbury, Connecticut, us, 06813![Canopy Life Sciences LLC](/api/image?src=https%3A%2F%2Fgeneral-board-default.s3.us-east-2.amazonaws.com%2Fpublic%2Fimages%2Fdesk-360x180.webp&w=640&q=75&f=webp)
Work at Canopy Life Sciences LLC
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Overview
Do you have the following skills, experience and drive to succeed in this role Find out below.Job Summary:
Our growing company is always seeking motivated and ambitious professionals with expertise in Medical Content Review.
At Canopy, we understand that the advertising environment has evolved and with it, so have the skills required for promotional and medical content review. In this new environment, you must understand and appreciate the legacy as well as provide creative, forward-looking ideas, approaches, and solutions to drive content that is both compelling and compliant. We look for applicants with a progressive mindset that are grounded in practiced principles to deliver a superior level of support to our clients.
The role of Associate Director, Medical Content Review is to act as the primary medical and scientific content reviewer and provide final approval for all medical and promotional assets for clients. This role does not have any direct reports.
The following are the general duties and expectations of the role:
· Represent Medical Affairs on the promotional review committee as the lead Medical Reviewer.
· Conduct medical review and provide guidance on rigor of data used in medical and promotional content to ensure scientific and medical accuracy.
· Effectively collaborate with Commercial, Regulatory, and Legal business partners to provide strategic input and drive alignment.
· Maintain ongoing communication and alignment with assigned therapeutic area peers in Medical Affairs for awareness and consistency with strategy.
Qualifications for the role include:
· An advanced science or medical degree (PharmD, PhD, MD, PA, NP, RN) strongly preferred.
· At least 3-5 years of direct promotional/medical review experience and be comfortable working independently in a fully remote role with minimal oversight.
· Demonstrated ability to critically analyze research design, methods, and outcome measures.
· Advanced knowledge of pharmaceutical guidelines and regulations.
· Demonstrated ability to critically analyze research design, methods, and outcome measures.
As a part of our full-time team, you are eligible for our Comprehensive Benefits including:
Medical, Dental and Vision Insurance
Disability Insurance and Life Insurance
401(k) program with company match
A balanced approach to work-life that offers a generous PTO program and Holidays.
This is a remote position.
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