Job summary
Job post source
This job is directly from Worldwide Clinical Trials
Job overview
The Senior Medical Writer role at Worldwide Clinical Trials involves leading medical writing for clinical trial documents across phases I-IV, impacting regulatory submissions and study communications globally.
Responsibilities and impact
The role requires preparing and leading the medical writing team on various clinical study documents, managing document templates, collaborating with other departments on regulatory documents, and serving as a publishing contact for clinical trial reports.
Compensation and benefits
The salary range is $80,735 to $160,265 depending on skills, experience, and location; benefits details are not specified.
Experience and skills
Candidates need a life science degree or equivalent, at least 4 years of medical writing experience, excellent English skills, knowledge of regulatory guidelines (ICH E3, E6, E9), and proficiency in Microsoft Office; travel availability is required.
Career development
The company offers ongoing training and career development opportunities within a dynamic global medical writing team.
Work environment and culture
Worldwide Clinical Trials values diversity, inclusion, collaboration, creativity, and supports a cohesive and accessible leadership environment where employees thrive.
Company information
Worldwide Clinical Trials is a global midsize CRO with over 3,500 employees focused on innovative clinical research to find cures for persistent diseases.
Team overview
The medical writing team is global, dynamic, and supported by leadership and peers, working closely with subject matter experts and regulatory strategists.
Job location and travel
The position is remote, supporting UK/US markets, with domestic and international travel required.
Unique job features
The role involves working on a wide range of regulatory documents across multiple regions and therapeutic areas, with leadership responsibilities in medical writing and template management.
Company overview
Worldwide Clinical Trials is a global contract research organization (CRO) that provides phase I-IV clinical trial services to the pharmaceutical and biotechnology industries. They specialize in therapeutic areas such as neuroscience, cardiovascular, metabolic, and rare diseases. Founded in 1986, the company has grown to operate in more than 60 countries, leveraging their scientific expertise and innovative technologies to deliver high-quality data and support drug development. Their revenue is primarily generated through service contracts with pharmaceutical companies, offering comprehensive clinical trial management, data analysis, and regulatory support.
How to land this job
Tailor your resume to emphasize your expertise in preparing Phase I-IV clinical study documents such as protocols, informed consent forms, clinical trial reports, and Investigator Brochures, highlighting your knowledge of regulatory requirements across the USA, Europe, and other regions.
Showcase your strong command of medical writing standards, including familiarity with ICH guidelines E3, E6, and E9, and your ability to manage document templates and publishing processes efficiently.
Apply through multiple platforms including Worldwide Clinical Trials' official careers page, LinkedIn, and other job boards where the position is listed to maximize your application visibility.
Connect with medical writing professionals and team members at Worldwide Clinical Trials on LinkedIn; open conversations by referencing recent company initiatives, expressing enthusiasm for their collaborative culture, or asking about the team’s approach to regulatory document challenges.
Optimize your resume for ATS by incorporating keywords from the job description such as 'medical writing,' 'clinical trial reports,' 'ICH E3/E6/E9,' 'protocol development,' and 'regulatory submissions' to ensure your resume passes initial automated screenings.
Leverage Jennie Johnson’s Power Apply feature to automate tailored resume customization, find all relevant application portals, and identify LinkedIn contacts in the medical writing division, freeing up your time to focus on interview preparation and networking.
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