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 the preparation of clinical study documents across all phases to support regulatory submissions and clinical development, impacting the quality and compliance of medical writing deliverables.
Responsibilities and impact
The role requires preparing and leading medical writing teams on Phase I-IV 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 ranges from $80,735 to $160,265 depending on skills, experience, and location. Benefits are not explicitly detailed but the company emphasizes a supportive and inclusive work environment.
Experience and skills
Candidates need a life science or related degree, at least 4 years of medical writing experience, excellent English communication, strong project management skills, knowledge of regulatory guidelines like ICH E3, E6, E9, and flexibility for domestic and international travel.
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 promotes a diverse, inclusive, collaborative, and supportive culture where employees are encouraged to be themselves and do their best work.
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 with peer, leadership, and administrative resources, working closely with subject matter experts across the company.
Job location and travel
The position is remote with expectations for domestic and international travel requiring a valid passport.
Unique job features
The role involves leadership in medical writing across multiple regulatory regions and phases, with opportunities to work on diverse documents and collaborate with various departments globally.
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 experience preparing and leading medical writing teams on Phase I-IV clinical study documents, including protocols, clinical trial reports, and regulatory submissions, as these are central to the Senior Medical Writer role at Worldwide Clinical Trials.
Highlight your knowledge of regulatory requirements and guidelines such as ICH E3, E6, and E9, and your ability to interpret complex clinical data clearly and concisely, which are key qualifications for this position.
Apply through multiple channels including Worldwide Clinical Trials' corporate careers page and LinkedIn to maximize your application visibility and ensure you meet all submission requirements.
Connect with current medical writers or team leads within Worldwide Clinical Trials on LinkedIn, using ice breakers like commenting on recent clinical trial innovations they shared or expressing genuine interest in their approach to regulatory document development.
Optimize your resume for ATS by incorporating keywords from the job description such as 'medical writing,' 'clinical trial reports,' 'regulatory submissions,' 'ICH guidelines,' and 'protocol development' to increase your chances of passing automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate the tailoring of your resume, identify multiple application portals, and suggest relevant LinkedIn contacts, allowing you to focus your energy on preparing for interviews and networking effectively.
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