Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC
Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC

Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC

London Temporary 36000 - 60000 £ / year (est.) Home office possible
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At a Glance

  • Tasks: Lead medical writing projects and create essential clinical documents.
  • Company: Join Syneos Health, a top biopharmaceutical solutions organisation dedicated to accelerating customer success.
  • Benefits: Enjoy fully remote work, career development, and a supportive culture that values diversity.
  • Why this job: Make a real impact in healthcare while collaborating with passionate professionals in a dynamic environment.
  • Qualifications: Bachelor's degree in relevant fields and experience in medical writing required; oncology knowledge preferred.
  • Other info: Work with a global team impacting 94% of all Novel FDA Approved Drugs.

The predicted salary is between 36000 - 60000 £ per year.

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you will collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we are able to create a place where everyone feels like they belong.

Job Responsibilities:

  • Acts as lead for assigned writing projects.
  • Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.
  • Develops or supports a variety of documents that include, but not limited to:
  • Clinical study protocols and clinical protocol amendments;
  • Clinical study reports;
  • Patient narratives;
  • Clinical development plans;
  • IND submissions and annual reports;
  • Integrated summary reports;
  • NDA and (e)CTD submissions;
  • Investigator brochures;
  • Clinical journal manuscripts, clinical journal abstracts, and client presentations.
  • Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
  • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
  • Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
  • Serves as peer reviewer on internal review team providing review comments on draft and final documents.
  • Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
  • Performs on-line clinical literature searches, as applicable.
  • Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
  • Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
  • Completes required administrative tasks within the specified timeframes.
  • Performs other work-related duties as assigned.
  • Qualifications:

    • Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.
    • Previous experience as a Senior Medical Writer working in a CRO or Pharma. Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as well as a familiarity with AMA style guide.
    • Demonstrated high degree of independence with effective presentation, proofreading, interpersonal, and leadership skills and ensure a team-oriented approach.
    • Strong proficiency in Word, Excel, PowerPoint, email, and Internet.
    • Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.
    • Needs experience writing clinical and submission ready documents.
    • Oncology / Auto-immune diseases experience.

    Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

    Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC employer: Syneos Health Careers

    Syneos Health is an exceptional employer that prioritises the growth and well-being of its employees, offering a supportive work culture where diversity and authenticity are celebrated. With a commitment to career development, comprehensive training, and a Total Self culture, employees can thrive in a fully home-based role while contributing to meaningful projects that impact lives globally. Join us to be part of a passionate team dedicated to innovation and excellence in biopharmaceutical solutions.
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    Contact Detail:

    Syneos Health Careers Recruiting Team

    StudySmarter Expert Advice 🤫

    We think this is how you could land Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC

    ✨Tip Number 1

    Familiarise yourself with the specific regulatory standards and guidelines mentioned in the job description, such as ICH-E3 and FDA regulations. This knowledge will not only help you during the interview but also demonstrate your commitment to the role.

    ✨Tip Number 2

    Network with current or former employees of Syneos Health on platforms like LinkedIn. Engaging with them can provide you with insider insights about the company culture and expectations, which can be invaluable during your application process.

    ✨Tip Number 3

    Prepare to discuss your experience with clinical and submission-ready documents in detail. Be ready to share specific examples of your work, especially in oncology or auto-immune diseases, as this aligns closely with the job requirements.

    ✨Tip Number 4

    Showcase your leadership and teamwork skills during interviews. Since the role involves collaboration across departments, emphasising your ability to work effectively in a team-oriented environment will make you a more attractive candidate.

    We think you need these skills to ace Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC

    Medical Writing Expertise
    Clinical Study Protocol Development
    Regulatory Knowledge (FDA, ICH)
    Document Review and Proofreading
    Statistical Analysis Plan Review
    Clinical Literature Search Skills
    Project Management
    Interpersonal Skills
    Presentation Skills
    Attention to Detail
    Familiarity with AMA Style Guide
    Ability to Interpret Clinical Data
    Experience in Oncology/Auto-immune Diseases
    Proficiency in Microsoft Word, Excel, PowerPoint
    Time Management

    Some tips for your application 🫡

    Tailor Your CV: Make sure your CV highlights relevant experience in medical writing, particularly in clinical and submission-ready documents. Emphasise your familiarity with FDA and ICH regulations, as well as any specific experience in oncology or auto-immune diseases.

    Craft a Compelling Cover Letter: In your cover letter, express your passion for the role and how your skills align with Syneos Health's mission. Mention your ability to work independently and your experience managing writing projects, as these are key aspects of the job.

    Showcase Your Writing Skills: Include samples of your previous medical writing work, if possible. This could be excerpts from clinical study protocols, reports, or any other relevant documents that demonstrate your proficiency in writing and adherence to regulatory standards.

    Highlight Team Collaboration: Since the role involves interacting with various departments, mention any past experiences where you successfully collaborated with cross-functional teams. This will show your ability to work within a team-oriented environment, which is crucial for this position.

    How to prepare for a job interview at Syneos Health Careers

    ✨Know Your Documents

    Familiarise yourself with the types of documents you'll be expected to write, such as clinical study protocols and reports. Being able to discuss these confidently will show your expertise and readiness for the role.

    ✨Understand Regulatory Standards

    Brush up on ICH-E3 guidelines and FDA regulations. Demonstrating your knowledge of these standards during the interview will highlight your suitability for the position and your commitment to compliance.

    ✨Showcase Your Independence

    Prepare examples that illustrate your ability to work independently and manage writing projects with minimal supervision. This is crucial for a Senior Medical Writer role, so be ready to discuss how you've successfully led projects in the past.

    ✨Highlight Team Collaboration

    Since the role involves interacting with various departments, be prepared to share experiences where you collaborated effectively with others. Emphasising your interpersonal skills will demonstrate that you can thrive in a team-oriented environment.

    Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC
    Syneos Health Careers
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    • Single Sponsor Senior Clinical Medical Writer - (fully home based) 6 month FTC

      London
      Temporary
      36000 - 60000 £ / year (est.)

      Application deadline: 2027-07-07

    • S

      Syneos Health Careers

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