Contract Medical Writer
- Employer
- Worldwide Clinical Trials
- Location
- Nottingham, GB
- Salary
- Competitive
- Start date
- 18 Nov 2020
- Closing date
- 1 Dec 2020
View more
- Discipline
- Medical Communications, Medical Writing
- Hours
- Part Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
RESPONSIBILITIES:
- 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.
OTHER SKILLS AND ABILITIES:
- 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).
REQUIREMENTS:
- 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.
- Available for domestic and international travel, including overnight stays (valid passport).
Company
Find out more about working for our company
Brief Company Description;
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
- Website
- https://www.worldwide.com/
- Mini-site
- Worldwide Clinical Trials
- Telephone
- +44 115 956 7711
- Location
-
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom
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