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Editing Specialist

4+ years
Not Disclosed
10 July 24, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About Fortrea

Fortrea, a global leader in Contract Research Organizations (CRO), is dedicated to scientific rigor and clinical development. With extensive experience spanning decades, we provide pharmaceutical, biotechnology, and medical device customers with a broad array of solutions across over 20 therapeutic areas. Our team of more than 19,000 professionals operates in over 90 countries, driving transformative advancements in drug and device development to benefit partners and patients worldwide.

Position Responsibilities

  • Document Review and Editing: Proofread and edit scientific, regulatory documents, safety reports, and other materials to ensure adherence to company or client conventions, styles, formats, and terminology.
  • Standard Language Development: Assist in creating standard language for documents.
  • Report Compilation: Help compile electronic versions of final reports and create associated PDF files, including bookmarking and hyperlinking as needed.
  • Document Formatting: Format final documents and potentially facilitate editor meetings.
  • Mentoring: Train and mentor editors and new writers on style guides.
  • Process Improvement: Identify and address process improvements to enhance editing group efficiency.
  • Communication: Handle internal and external communication to gather necessary inputs and ensure high-quality deliverables.
  • Compliance and Accountability: Implement consistent, efficient processes to meet timelines and deliverables while ensuring compliance with regulatory requirements.
  • Customer Service: Cultivate a high standard of customer service and assume accountability for deliverables.
  • Additional Tasks: Perform additional activities as required based on project needs or managerial direction, following relevant training.

Join Our Team

Fortrea is on the lookout for driven problem-solvers and creative thinkers who are passionate about overcoming challenges in clinical trials. Our commitment to revolutionizing the development process ensures the rapid delivery of life-changing therapies to patients. By joining us, you will be part of a collaborative environment that promotes personal growth and allows you to make a significant global impact.

Fortrea is an Equal Opportunity Employer:

We are committed to fostering diversity and inclusion within our workforce. Fortrea does not tolerate harassment or discrimination of any kind and makes employment decisions based on business needs and individual qualifications. We do not discriminate based on race, religion, color, national origin, gender (including pregnancy and other medical conditions), family or parental status, marital status, sexual orientation, gender identity or expression, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all qualified individuals to apply.

For details on how we collect and store your personal data, please review our Privacy Statement at www.fortrea.com.