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Medical Writing Manager – North America (US/Canada)
Medical Writing – Remote
A global medical writing and consulting organization is seeking a Medical Writing Manager to support its continued growth in delivering regulatory documentation for the international pharmaceutical industry. This position reports directly to the Director of Medical Writing and plays a key leadership role within a collaborative team of experienced professionals. The organization is known for providing high-quality medical writing services that go beyond writing, involving strategic input and coordination in clinical development programs across various therapeutic areas.
Note: Candidates must be located in the United States or Canada.
Job Overview
:As a Medical Writing Manager, your responsibilities will include
- :Providing line management for a team of medical writers
- .Offering resource oversight and weekly guidance
- .Supporting professional development through regular (e.g., quarterly) check-ins
- .Conducting annual and ad-hoc performance reviews
- .Monitoring employee time and utilization
- .Reinforcing company values and mission to maintain a shared sense of purpose
- .Participating in management-level initiatives and strategy discussions
- .Engaging in business development activities such as delivering presentations, contributing to strategic planning, or representing the company in client meetings
- .Continuing to contribute to client writing projects with a reduced writing workload to allow for management responsibilities
.
Required Experience and Qualification
- s:2 years of line-management experience leading a team of medical writer
- s.At least 7 years of medical regulatory writing experience in pharmaceutical, biotech, or CRO setting
- s.Proven success as a Lead Medical Writer on various regulatory document types, including large-scale projects with international teams (e.g., submission dossiers, response documents
- ).Experience coordinating project-level activities, including resource management, quality control oversight, and process plannin
- g.Ability to conduct cost-benefit analyses to inform decision-making (e.g., resource assignment, conflict resolution
- ).Strong interpersonal, leadership, decision-making, and communication skill
s.
Compensation and Benefi
- ts:Competitive base sal
- aryAnnual bonus eligibility based on individual and company performan
- ce.Generous paid time off, including vacation, holidays, birthday, and sick lea
- ve.Comprehensive benefits package, including medical, dental, vision, disability, and life insuran
- ce.401(k) plan with company mat
- ch.Membership in professional associations and sponsored attendance at key industry conferenc
- es.Additional perks such as wellness programs and team-building even
Medical Writing Manager – North America (US/Canada)
Medical Writing – Remote
A global medical writing and consulting organization is seeking a Medical Writing Manager to support its continued growth in delivering regulatory documentation for the international pharmaceutical industry. This position reports directly to the Director of Medical Writing and plays a key leadership role within a collaborative team of experienced professionals. The organization is known for providing high-quality medical writing services that go beyond writing, involving strategic input and coordination in clinical development programs across various therapeutic areas.
Note: Candidates must be located in the United States or Canada.
Job Overview
:As a Medical Writing Manager, your responsibilities will include
- :Providing line management for a team of medical writers
- .Offering resource oversight and weekly guidance
- .Supporting professional development through regular (e.g., quarterly) check-ins
- .Conducting annual and ad-hoc performance reviews
- .Monitoring employee time and utilization
- .Reinforcing company values and mission to maintain a shared sense of purpose
- .Participating in management-level initiatives and strategy discussions
- .Engaging in business development activities such as delivering presentations, contributing to strategic planning, or representing the company in client meetings
- .Continuing to contribute to client writing projects with a reduced writing workload to allow for management responsibilities
.
Required Experience and Qualification
- s:2 years of line-management experience leading a team of medical writer
- s.At least 7 years of medical regulatory writing experience in pharmaceutical, biotech, or CRO setting
- s.Proven success as a Lead Medical Writer on various regulatory document types, including large-scale projects with international teams (e.g., submission dossiers, response documents
- ).Experience coordinating project-level activities, including resource management, quality control oversight, and process plannin
- g.Ability to conduct cost-benefit analyses to inform decision-making (e.g., resource assignment, conflict resolution
- ).Strong interpersonal, leadership, decision-making, and communication skill
s.
Compensation and Benefi
- ts:Competitive base sal
- aryAnnual bonus eligibility based on individual and company performan
- ce.Generous paid time off, including vacation, holidays, birthday, and sick lea
- ve.Comprehensive benefits package, including medical, dental, vision, disability, and life insuran
- ce.401(k) plan with company mat
- ch.Membership in professional associations and sponsored attendance at key industry conferenc
- es.Ongoing professional development opportuniti
- es.Additional perks such as wellness programs and team-building even
ts.
Seniority level
Seniority level
Not Applicable
Employment type
Job function
Job function
Writing/EditingIndustries
Pharmaceutical Manufacturing
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