CTC Resourcing Solutions is a specialist staffing organization based in Basel, London, and Munich providing flexible staffing to the pharmaceutical industry across Europe. They are currently looking for a Senior Medical Writer to be based in Berkshire, England, West Lothian, Scotland, or home-based. The role would involve leading global writing teams to develop clinical trial documents for drugs and medical devices. Qualifications include a science degree, medical writing experience, and experience preparing clinical study protocols and reports. The successful candidate would receive a competitive salary and benefits package.

1. Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded in Basel, Switzerland in 1997, is a specialist staffing organisation based in
Basel, London and Munich, providing flexible resourcing solutions to the pharmaceutical industry across Europe,
with contract and permanent placements in clinical development, data management, statistics, regulatory affairs
and medical marketing.
For one of our clients, we are currently looking for a
Senior Medical Writer
Reference Number: 50-13-819-SMW-W
Type of placement: Permanent
Location: Berkshire, England or West Lothian, Scotland or Home-Based
Our client is the word’s leading provider of biopharmaceutical services. With a network of > 27,000
professionals working in over 80 countries, it has helped develop or commercialise all of the top 50
best selling drugs on the market. Through its application of extensive therapeutic, scientific and
analytical expertise, our client helps biopharmaceutical and health sciences customers navigate the
increasingly complex landscape with more predictability to enable better outcomes.
Main Responsibilities:
 Lead global writing teams for the development of clinical trial documents (e.g. Clinical Study
Reports, Clinical Study Protocols & Statistical Analysis Plans) for investigational drugs,
biopharmaceuticals or medical devices
 Confidently work with others to develop study protocols from brief outlines, and take
responsibility for a variety of clinical and regulatory documents for a range of international and
local sponsors
 Understand and interpret study objectives and clinical trial data as well as the regulatory and
scientific requirements of the documents
 Interact directly with international project team members and clients regarding the medical
writing needs of global trials or programmes
 Proactively manage your own deliverables identifying and responding to potential challenges
with solutions
 Balance project lead roles with quality control and review responsibilities for colleagues
 Work with minimal direction, identify project needs, and create and deliver against project
timelines
 Mentor/train junior staff, as assigned
Qualifications and Experience:
 Bachelor of Science (Honours) degree, advanced degree preferred
 Relevant experience as a medical writer
 Extensive hands-on experience in preparing clinical study protocols and reports
 Demonstrate a solid scientific academic background, together with existing clinical and / or
regulatory medical writing experience
Our offer:
 Competitive basic salary
 Bonus
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK
Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch

2. Flexible benefits package including, but not limited to:
 Contributory Pension
 Private Health Insurance
 Permanent Health Insurance
 Life Assurance
 Additional benefits based on health and well-being
 25 days holiday increasing with length of service
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK
Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch