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 phases I-IV, impacting regulatory compliance and clinical development.
Responsibilities and impact
The role requires preparing and leading medical writing teams on study documents like protocols, informed consent forms, clinical trial reports, and regulatory submissions, ensuring adherence to global regulations and coordinating with other departments.
Compensation and benefits
The salary ranges from $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 communication, strong project management, regulatory knowledge, and flexibility for 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 with accessible leadership and values passion and purpose.
Company information
Worldwide Clinical Trials is a global midsize CRO with over 3,500 employees focused on innovative clinical research to improve patient lives.
Team overview
The medical writing team is global, dynamic, and supported by leadership and peers, working closely with subject matter experts and other departments.
Job location and travel
The position is remote with potential domestic and international travel requiring a valid passport.
Unique job features
The role involves working on a wide range of therapeutic areas and documents, with opportunities to liaise with regulatory authorities and manage document templates 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
Position your resume to highlight your expertise in medical writing for Phase I-IV clinical trial documents, emphasizing your experience with protocols, clinical trial reports, and regulatory submissions relevant to the US, Europe, and other regions.
Stress your knowledge of regulatory guidelines such as ICH E3, E6, and E9, and your ability to interpret complex clinical data into clear, concise written documents.
Apply through multiple channels including Worldwide Clinical Trials' corporate careers page, LinkedIn job postings, and other reputable job boards to maximize exposure.
Connect on LinkedIn with professionals in Worldwide Clinical Trials' medical writing or clinical operations teams; use ice breakers like commenting on recent company innovations or asking about their experiences with cross-functional collaboration within the company.
Optimize your resume for ATS by incorporating keywords from the job description such as 'medical writing,' 'clinical trial reports,' 'ICH guidelines,' 'protocol development,' and 'regulatory submissions' to ensure it passes initial screenings.
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