Remote Medical Writing Manager/Senior Manager
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Trilogy Writing & Consulting, an Indegene company, is currently looking to hire a Medical Writing Manager/Senior Manager, reporting directly to the Director of Medical Writing, to support our growing company in producing regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our writers are integral members of clinical development teams supporting the writing and coordination of successful documentation across a broad spectrum of therapeutic areas. As our company continues to expand, there is room to develop with us and your ideas will form our future together. For further insight into who we are and what we do, please explore our website (www.trilogywriting.com).
Applicants must live in Canada and be authorized to work for any employer in Canada (we are unable to sponsor or take over sponsorship of an employment visa at this time); this is a fully remote position.
Job Overview:
As a Medical Writing Manager/Senior Manager, you will:
- Provide line management of a group of medical writers.
- Provide resource oversight and guidance on a weekly basis.
- Oversee professional development including regular (i.e. quarterly) meetings with all members of the honeycomb.
- Conduct annual and ad-hoc performance reviews for all members of the honeycomb.
- Oversee each employee’s time and utilization.
- Regularly reinforce the company’s values and purpose to maintain a sense of shared values, purpose, mission, and vision
- Participate in Trilogy management-level activities.
- Participate in business development activities such as giving talks or workshops on behalf of Trilogy, participating in management meetings to discuss strategic developments for the company, or representing Trilogy at meetings with clients.
- In addition, continue writing on client projects but have a reduced writing workload to accommodate these management activities.
Required experience and qualifications (professional skills) for this role:
- Experience managing a team of medical writers in a line-management function for a minimum of 2 years.
- A minimum of 8 years of medical regulatory writing experience in a pharmaceutical, biotech, or CRO environment.
- Demonstrated ability and experience as a Lead Medical Writer on multiple types of regulatory documents/writing projects, including complex, multiple-document projects with global,
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