A leading biotechnology and pharmaceutical company in the RNA space is looking to expand their clinical writing team with a Sr. Manager Medical Writing for a 6 month contract position. This Sr. Manager will aid clinical project teams in completing their clinical document deliverables, as well as be self-motivated, detail-oriented, and be flexible in their workload and timeline management.
Responsibilities and Requirements:
· Senior Clinical & Regulatory Writing experience (IB’s, CSR’s, Protocols, etc)
· Served as lead medical writer, with previous proven leadership experience with cross functional team
· CRO oversight / Outsourced work management
· Experience in Vaccines and Infectious Diseases
· Experience working in a fast-paced environment across all responsibilities
· Management of timelines and deliverables
· Minimum of 6-8 years Medical Writing with at least 5 years of pharmaceutical or biotech experience, or equivalent experience
· Veeva Vault – highly preferred
What this client can offer you:
· Earnings: Competitive hourly rate of $120/hr
· Fully Remote Work, 40 hours/week
· Contract Length = 6months, but likely to extend, conversion to permanent possible
· Opportunity to work at a leading pharmaceutical and biotechnology company that expects to continue rapid growth
· Fantastic company culture
· Medical, Dental, and Vision insurance
To apply to this role or to learn about other similar roles, please email me at h.boehm@sciproglobal.com.