Medical Writer

hace 1 semana


Barcelona, Barcelona, España Thermo Fisher Scientific A tiempo completo
At Thermo Fisher Scientific, you can find meaningful work that has a positive impact on a global scale. Join our team in bringing our Mission to life - helping our customers create a healthier, cleaner, and safer world. We provide our teams with the resources needed to achieve individual career goals while advancing science through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of new frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital, and decentralized clinical trial services. Your dedication to delivering quality and accuracy will enhance health outcomes that people and communities rely on, both now and in the future. Key Purpose: We are thrilled to expand our Medical Writing FSP Team in EMEA. This role can be done remotely from any location in EMEA. We are seeking a Medical Writer to focus on a client in the FSP space; experience in Immunology, Oncology, or Vaccines would be beneficial but not mandatory. The writer will produce high-quality medical and scientific content from planning through to delivering final drafts to internal and external clients. You will collaborate with clients internally and externally, facilitating effective communication that leads to operational excellence. Primary Responsibilities:
  • Serves as the main author for routine documents such as clinical study reports and study protocols, and compiles data from clinical studies.
  • Might assist with more complex clinical and scientific documents at the program level, including IBs, INDs, and MAAs.
  • Ensures adherence to quality processes and requirements for assigned documents. Might help in identifying best practices for optimal results.
  • May be involved in program management tasks, such as developing timelines, budgets, and forecasts for deliverables.
  • Represents the department in project launch meetings, review meetings, and project team meetings.
Education and Experience: Bachelor's degree in a scientific field or equivalent, plus relevant academic / vocational qualifications. Previous experience equivalent to 2+ years is required. Preferred experience in the pharmaceutical/CRO industry and advantageous experience in scientific writing and the Immunology, Oncology, or Vaccines fields. Skills and Qualifications:
  • Strong medical writing skills, including grammatical, editorial, and proofreading skills.
  • Ability to interpret and present complex data accurately and concisely.
  • Strong administrative, organizational, and planning skills with attention to detail and quality.
  • Able to work independently and as part of a team effectively.
  • Excellent oral and written communication skills.
  • Good understanding of regulatory documentation and the drug development process.
  • Demonstrates good judgment and decision-making skills.
  • Proficient in computer skills, familiar with client templates; Knowledgeable about document management systems and other relevant applications (e.g., Excel, Outlook).
Employee Benefits: At PPD clinical research services, we hire the best, develop ourselves and each other, and acknowledge the strength of working as a unified team. We recognize your desire to grow both professionally and personally in your career. Therefore, at PPD clinical research services, you will have access to development opportunities to help you realize your full potential. In addition to a competitive salary, we offer a comprehensive benefits package focused on employee health and well-being. We promote a healthy work-life balance at PPD clinical research services. We have experienced sustainable growth year after year and continue to foster a collaborative environment where colleagues share knowledge and enjoy working together. Although we are a global organization, we maintain a close-knit local feel. Our Mission is to empower our customers to create a healthier, cleaner, and safer world. As a team of over 100,000 colleagues, we uphold a common set of values - Integrity, Intensity, Innovation, and Involvement. Together, we strive to accelerate research, tackle complex scientific challenges, drive technological innovation, and support patients in need. Join PPD, part of Thermo Fisher Scientific, to #BeginYourJourney where diverse experiences, backgrounds, and perspectives are embraced.

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