Worldwide Clinical Trials

Senior Medical Writer - UK/US - Remote

REMOTEPosted 19 days ago

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 that support drug development and regulatory submissions globally.

  • Responsibilities and impact

    The role requires preparing and leading the creation of Phase I-IV clinical study documents, managing document templates, collaborating with other departments on regulatory submissions, and serving as a publishing contact for clinical trial reports.

  • Compensation and benefits

    The salary range is $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

    Candidates need a life science degree or equivalent, at least 4 years of medical writing experience, excellent English communication, regulatory knowledge (ICH E3, E6, E9), strong project management skills, and availability 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 fosters a diverse, inclusive, and collaborative culture with accessible leadership and supportive teams, encouraging employees to thrive 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 develop 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, supporting UK and US markets, with travel required domestically and internationally.

  • Unique job features

    The role offers the chance to work on a wide range of therapeutic areas and regulatory documents, with leadership responsibilities and involvement in high-level clinical development discussions.

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 preparing and leading medical writing teams on Phase I-IV clinical study documents, emphasizing protocols, clinical trial reports, and regulatory compliance across multiple regions including the USA and Europe.

  • Focus on showcasing your strong knowledge of regulatory guidelines like ICH E3, E6, and E9, your ability to interpret clinical data clearly, and your project management skills managing multiple deadlines independently.

  • Apply through Worldwide Clinical Trials' official corporate careers page and LinkedIn job postings to maximize your application visibility and ensure you are seen by different recruiting teams.

  • Connect with current medical writers or team leads at Worldwide Clinical Trials on LinkedIn; start conversations by complimenting recent company innovations, asking about their experience with cross-functional collaboration, or inquiring about the culture within the medical writing team.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'medical writing,' 'clinical trial reports,' 'regulatory requirements,' 'ICH guidelines,' and 'project management' to pass automated screenings effectively.

  • Use Jennie Johnson's Power Apply feature to automate multi-channel applications, tailor your resume with relevant keywords, and identify LinkedIn contacts for networking, allowing you to focus your energy on preparing for interviews and career growth.

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