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 teams to prepare critical clinical study documents, impacting the quality and compliance of clinical trial reporting globally.
Responsibilities and impact
The candidate will prepare and lead the creation of Phase I-IV study documents, manage document templates, collaborate with other departments on regulatory submissions, and serve as a publishing contact for clinical trial reports.
Compensation and benefits
The salary ranges from $80,735 to $160,265, with compensation varying by skills, experience, and location; specific benefits are not detailed but the company emphasizes a supportive and inclusive work environment.
Experience and skills
Requires a life science or related degree with at least 4 years of medical writing experience, excellent English communication, strong project management, regulatory knowledge (ICH E3, E6, E9), and flexibility for domestic and international travel.
Career development
The role offers ongoing training and career development opportunities within a dynamic global medical writing team.
Work environment and culture
Worldwide Clinical Trials promotes a diverse, inclusive, collaborative, and supportive culture with accessible leadership and a focus on enabling professionals to thrive.
Company information
Worldwide Clinical Trials is a global midsize CRO with over 3,500 employees, focused on innovative clinical research to advance treatments for persistent diseases.
Team overview
The medical writing team is global, dynamic, and well-supported, working closely with subject matter experts and regulatory strategists across the company.
Job location and travel
The position is remote, with requirements for domestic and international travel including overnight stays.
Unique job features
The role involves leadership in medical writing across multiple regulatory regions and therapeutic areas, with opportunities to work on diverse document types and regulatory submissions.
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 highlight your expertise in preparing and leading medical writing for Phase I-IV clinical trial documents, emphasizing familiarity with protocols, informed consent documents, clinical trial reports, and regulatory compliance across USA, Europe, and other regions.
Showcase your proficiency in collaborating with cross-functional teams including regulatory strategists and clinical methodologists, as well as your ability to manage document templates and publishing coordination.
Apply to the Senior Medical Writer role through multiple platforms such as Worldwide Clinical Trials' official corporate career page and LinkedIn to maximize your application visibility.
Connect with current medical writers or team leads at Worldwide Clinical Trials on LinkedIn, using ice breakers like commenting on their recent publications or expressing interest in their approach to regulatory document development.
Optimize your resume for ATS by incorporating keywords from the job description such as 'ICH E3, E6, E9 guidelines,' 'clinical trial reports,' 'medical writing,' 'regulatory compliance,' and 'project management' to ensure your resume passes automated screenings.
Use Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and facilitate networking outreach, allowing you to focus your energy on preparing for interviews and career growth.
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