Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
QC Specialist, Medical Communications
Job ID R0000037349 , IndiaResponsibilities:
- 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), with knowledge of IT and digital solutions.
- Strong attention to detail and accuracy, ability to manage and prioritize multiple, detailed activities, results-orientated with fast and focused execution.
- 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, and values teamwork, collaboration, and innovation.
- Prior experience working in any of the therapeutic areas of Cardiovascular Renal Metabolism (CRM), Respiratory, Inflammation, Immunology, Oncology would be advantageous
#LI-REMOTE
Recently Viewed Jobs
You have not recently viewed any jobs
View all jobs