QC Specialist, Medical Communications

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6 hours ago

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Parexel

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Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

📋 Description

• Cross check scientific information against cited references and ensure medical accuracy (fact check) • Ensure consistency with product label where applicable; and verify presence of essential information • Correct interpretation of scientific data from reference/sources, alignment/formatting of content as per style guides/journal guidelines/congress guidelines • Ensure consistency of scientific content across different sections (including text, figures, tables) accurate bibliography/in-text citation and alignment of figures/graphs as per branding guidelines • Confirm that every sentence is source annotated, and each source annotation matches with respective reference and vice versa • Ensure that information is presented in a neutral manner without any interpretations and/or author’s conclusion • Track work and communicate with client team on job reviews, prioritization etc., through emails and teleconferencing if needed • Participate in meetings, as required, to liaise with client stakeholders and resolve partially accepted or rejected comments after discussing with key stakeholders (med affairs lead, regulatory etc.) • Participate in assigned training programs and work on assignments as per requirement • Adherence to quality, timelines, confidentiality and security compliance

🎯 Requirements

• Experienced Medical Writer (1-2 years), with a scientific background and degree (PharmD, MD, PhD or Masters) • Strong attention to detail and accuracy, ability to manage and prioritize multiple, detailed activities • Good communication, coordination and time management skills • Ability to work within a team or across multiple teams (including remotely) as well as independently • Fluent in oral and written English with high level of communication skills • Prior experience working in any of the therapeutic areas of Cardiovascular Renal Metabolism (CRM), Respiratory, Inflammation, Immunology, Oncology would be advantageous

🏖️ Benefits

• Professional development opportunities