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emplois Medical Writer

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    • The Senior Medical Writer is a key contributor within the medical writing team, responsible for developing clear, accurate, and engaging scientific content…
    • This role serves as the lead medical writer for assigned clients, brands, or therapeutic areas and contributes to additional projects as required.
    • 5+ years of experience as a medical writer in the sponsor and/or CRO setting.
    • BS degree or equivalent in a scientific or medical discipline with relevant…
    • Minimum 4 years of regulatory medical writing experience.
    • At least 2 years as a medical writing project lead.
    • Interpreting clinical data and translating results…
    • Experience mentoring associate or junior medical writers on scientific content quality and project execution.
    • Klick is hiring a Senior Medical Writer to develop…
    • Mentors and leads less experienced medical writers on complex projects, as necessary.
    • Manages medical writing activities associated with individual studies,…
    • Perform literature searches to support senior medical writers.
    • Act as a lead medical writer in the preparation of clinical documents or scientific publications.
    • Performs peer review of documents written by other medical writers, as required.
    • Supervises, trains, and mentors less experienced medical writers, as necessary.
    • Supervises and mentors less experienced medical writers, as necessary.
    • Performs peer review of documents written by other medical writers, as required.
    • 5+ years of experience as a medical writer in the sponsor and/or CRO setting.
    • BS degree or equivalent in a scientific or medical discipline with relevant…
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Job Post Details

Sr. Medical Writer (CA) - job post

Six Degrees Medical Consulting
4.0 étoile(s) sur 5
Canada
Temps plein
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Détails du poste

Type de poste

  • Temps plein

Lieu

Canada

Description complète du poste

Job Summary

The Senior Medical Writer is a key contributor within the medical writing team, responsible for developing clear, accurate, and engaging scientific content across a range of medical communication deliverables. This role combines strong scientific understanding with advanced writing skills and growing leadership in client and project management. The Senior Medical Writer ensures that content reflects strategic objectives and scientific integrity while supporting and mentoring junior team members.

Essential Job Functions

Content Creation:

  • Research and write a variety of medical communications materials including summaries, slides, meeting reports, manuscripts, and digital content
  • Incorporate client feedback effectively and professionally into revised deliverables
  • Attention to detail and ability to communicate complex information clearly and accurately
  • Creative-thinking skills to visualize and tell a story with graphics
  • Critically evaluate data from scientific literature, clinical studies, and other sources to ensure content accuracy and credibility
  • Knowledge of the global pharma industry and the associated regulatory and compliance requirements combined with knowledge of the global drug development process and product market needs



Therapeutic Area Development

  • Knowledge and proficiency across relevant therapeutic areas, including disease states, treatment landscapes, and emerging data
  • Apply therapeutic understanding to ensure content is contextually accurate, strategically aligned, and appropriate for target audiences
  • Understanding of client objectives, therapeutic priorities, and communication preferences over time



Project Leadership:

Take ownership of assigned projects and deliverables, managing timelines, client expectations, and internal review processes to ensure on-time, high-quality delivery



    Client Interaction:

    Participate in client calls and meetings, offering scientific input and demonstrating understanding of client needs and therapeutic landscapes



      Collaboration:

      Work closely with account management, creative, and strategy teams to develop integrated and scientifically sound communication programs



        Quality and Compliance:

        Ensure that all work adheres to agency quality standards, style guides, and industry guidelines (eg compliance, regulatory & legal)



          Mentorship:

          Support the development of junior writers through coaching, feedback, and sharing of best practices



            Professional Growth:

            Seek and apply feedback from mentors and peers; actively develop writing skills and therapeutic knowledge



              Minimum Qualifications:

              • Education:
                • Advanced degree in a scientific or medical discipline (PhD, PharmD, MD, MSc, or equivalent)
              • Experience:
              • 3–5+ years of experience in medical communications or related industry
              • Knowledge and Abilities:
              • Strong organizational skills, ability to set priorities to meet operational deadlines and juggle multiple projects in a fast-paced environment
              • Proficiency in Microsoft Office applications with a focus on presentations, graphics, and templates
              • Self-direction with integrity, positive attitude, confidence, speed, and with a passion for Reverba Global’s vision, mission, and values

              Work Environment
              This job operates in a professional in-person and virtual office environment. This role routinely involves standard office equipment such as computers and phones.

              Physical Demands
              The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

              This is largely a sedentary role - prolonged periods of sitting at a desk and working on a computer. Also includes travel and onsite execution of events as needed.

              Position Type/Expected Hours of Work
              This is a full-time position.

              Other Duties
              Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

              EEO Statement
              Reverba provides equal employment opportunities to all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, sexual orientation, marital status, religion, age, disability, gender identity, results of genetic testing, or service in the military. Equal employment opportunities applies to all terms and conditions of employment, including hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation, and training.

              We strongly encourage applications from Indigenous peoples, racialized individuals, women, persons with disabilities, and LGBTQ+ individuals.

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