Job title: PRN Phase I Medical Writer -US/CANADA REMOTE
Company: Worldwide Clinical Trials
Job description: Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.Why WorldwideWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!What the PRN Medical Writer doesThe PRN Medical Writer is responsible for carrying out medical writing activities in accordance with client specifications in a timely, accurate, and efficient manner, within budget and to the written, scientific, and ethical standards in accordance with regulatory requirements and WCT standard operating procedures (SOPs).What you will do
- Prepare study documents such as protocols, informed consent documents, clinical study reports (CSRs), patient narratives, and other study documents in accordance with regulatory requirements and WCT SOPs.
- Coordinate internal and client document review cycles.
- Attend project-related meetings, as needed.
- Review and QC documents, as needed.
- Serve as publishing point-of-contact in conjunction with the document coordinator to publish CSRs or other documents, as needed.
- Identify and appropriately communicate risks associated with document delivery and propose mitigation plans.
- Advise project teams and clients on medical writing-related issues.
- Complete project-specific and company training, as assigned.
- Perform other duties as assigned.
What you will bring to the role
- Excellent written and spoken English, able to accurately interpret data and express findings in a clear and concise written manner.
- Project/time management and organizational skills, as well as the ability to work independently.
- Flexibility in meeting challenging deadlines and changing requirements while working on multiple projects.
- Comprehensive Microsoft Office, especially WORD but also PowerPoint and Excel skills, as well as internet skills.
- Ability to communicate with professionals from a variety of backgrounds.
- Attention to detail-style, consistency, grammar, syntax, scientific accuracy.
- Knowledge of applicable regulatory requirements and guidelines (in particular ICH E3, E6, and E9).
Your experience
- University/college degree (life science or related allied health profession) and American Medical Writers Association Certification or equivalent combination of education and experience that provides the individual with the required knowledge, skills, and abilities to perform the above responsibilities.
- Graduate degree preferred.
- Minimum of 1 year of clinical pharmaceutical industry experience.
Why WorldwideWe love knowing that someone is going to have a better life because of the work we do.To view our other roles, check out our careers page at ! For more information on Worldwide, visit or connect with us on .
Expected salary:
Location: Canada – USA
Job date: Sun, 26 May 2024 01:36:12 GMT
