Job summary
Job post source
This job is from a recruiting firm hiring for a separate company
Job overview
The Senior Medical Writer role involves producing high-quality regulatory and clinical documents for a global pharmaceutical company, contributing to regulatory compliance and clinical study communication.
Responsibilities and impact
The candidate will author clinical and regulatory documents, manage writing activities across projects, ensure alignment with regulatory standards, and collaborate with the global team.
Compensation and benefits
The position is a 12-month contract, full-time (40 hrs/week), and fully remote; no specific salary or benefits details are provided.
Experience and skills
Candidates must have a relevant life sciences degree (Ph.D. with 4+ years experience or BA/BS with 7+ years), experience authoring clinical/regulatory documents, and knowledge of ICH and management systems.
Work environment and culture
The role is fully remote and part of a dynamic global team emphasizing collaboration, attention to detail, and innovation in medical writing.
Company information
The job is for a global pharmaceutical company represented by a recruiting firm called Real.
Team overview
The candidate will join a dynamic global team focused on medical writing.
Job location and travel
Fully remote work arrangement.
Unique job features
The role offers the opportunity to work on high-quality regulatory and clinical documents within a global pharmaceutical setting with a focus on innovation.
Company overview
Real is a technology company specializing in mental health and wellness, offering a platform that provides accessible, affordable, and personalized mental health care. They generate revenue through subscription-based services, where users pay for access to therapy sessions, mental health programs, and self-care tools. Founded in 2019 by Ariela Safira, Real has gained attention for its innovative approach to mental health, combining digital tools with professional support to democratize mental health care. The company emphasizes inclusivity and aims to reduce the stigma associated with seeking mental health support.
How to land this job
Position your resume to highlight your experience in authoring clinical and regulatory documents, emphasizing your ability to craft scientifically accurate and high-quality materials like protocols and clinical study reports.
Focus on showcasing your familiarity with ICH guidelines, regulatory standards, and clinical trial data interpretation to align with the job's core requirements.
Apply through multiple platforms including Real's corporate website and LinkedIn to maximize your chances of being noticed for the Senior Medical Writer role.
Connect with professionals in Real's medical writing or regulatory affairs divisions on LinkedIn; use ice breakers such as commenting on recent regulatory changes or expressing interest in their approach to clinical documentation.
Optimize your resume for ATS by including keywords like 'medical writing,' 'clinical study reports,' 'regulatory documents,' 'ICH guidelines,' and 'clinical trial data interpretation' to ensure it passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify optimal application channels, and discover LinkedIn contacts for networking, allowing you to focus your energy on preparing for interviews and refining your skills.
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