Current jobs related to Clinical Trials Medical Writer - London, Greater London - SML Medical Supplies Inc
-
Senior Medical Writer
3 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeAbout the RoleWorldwide Clinical Trials is seeking a Senior Medical Writer to join our team in Europe. As a Senior Medical Writer, you will be responsible for creating high-quality clinical documents that support the development of new medications.Key ResponsibilitiesDevelop and maintain clinical documents, including clinical study reports, protocols, and...
-
Senior Medical Writer
3 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeAbout the RoleWorldwide Clinical Trials is seeking a Senior Medical Writer to join our team in Europe. As a Senior Medical Writer, you will be responsible for creating high-quality clinical documents that support the development of new medications.Key ResponsibilitiesDevelop and maintain clinical documents, including clinical study reports, protocols, and...
-
Senior Medical Writer and Therapeutic Specialist
24 hours ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeAt Worldwide Clinical Trials, we are a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to advance new medications from discovery to reality.We offer a competitive salary of $120,000 - $180,000 per annum, based on experience, as well as a range of benefits including health...
-
Senior Medical Writer
1 month ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeJoin Our Team at Worldwide Clinical TrialsWe are a leading global contract research organization (CRO) working in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications.Our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases enables us to develop...
-
Senior Medical Writer
1 month ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeJoin Our Team at Worldwide Clinical TrialsWe are a leading global contract research organization (CRO) working in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications.Our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases enables us to develop...
-
Senior Medical Writer
3 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeAbout the RoleAs a Senior Medical Writer at Worldwide Clinical Trials, you will be part of a talented team of 3,000+ professionals spanning 60+ countries. We are united in our cause to improve the lives of patients through new and innovative therapies.Our ExpertiseWe have a dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and...
-
Senior Medical Writer
4 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeAbout UsWorldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions for advancing new medications.Our MissionWe are united in our cause to improve the lives of patients through innovative therapies. Our dedicated team of 3,000+ professionals...
-
Medical Director, Medical Affairs Leader
2 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeJob Title: Medical Director, Medical AffairsAbout the Role:As a Medical Director, Medical Affairs at Worldwide Clinical Trials, you will lead the development and implementation of medical strategies to support the growth and success of our clients. You will work closely with cross-functional teams to drive medical insights and deliver value to our...
-
Medical Director, Medical Affairs Specialist
4 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeCompany Overview:Worldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions for advancing new medications.Job Summary:We are seeking a highly skilled Medical Director to join our team. As a key member of our medical leadership, you will be...
-
Medical Writer Specialist
4 weeks ago
London, Greater London, United Kingdom Translate Plus Full timeJob Title: Medical WriterJob Description:We are seeking a highly skilled Medical Writer to join our team at Translate Plus. As a Medical Writer, you will be responsible for communicating complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.Responsibilities:Clinical and...
-
Medical Writer Specialist
4 weeks ago
London, Greater London, United Kingdom Translate Plus Full timeJob Title: Medical WriterJob Description:We are seeking a highly skilled Medical Writer to join our team at Translate Plus. As a Medical Writer, you will be responsible for communicating complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.Responsibilities:Clinical and...
-
Senior Medical Writer
5 days ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeAbout the RoleAs a Senior Medical Writer with our Europe-based team, you will work closely with global project leaders to develop customized solutions for biotechnology and pharmaceutical companies.Our ExpertiseWe specialize in cardiovascular, metabolic, neuroscience, oncology, and rare diseases, ensuring flexible plans and swift problem-solving for our...
-
Medical Writer
2 weeks ago
London, Greater London, United Kingdom MMS Full timeMMS is a leading Contract Research Organization (CRO) that provides innovative data-focused services to the pharmaceutical, biotech, and medical device industries. With a proven scientific approach to complex trial data and regulatory submission challenges, MMS supports clients in creating compelling submissions that meet rigorous regulatory standards.Key...
-
Medical Director, Medical Affairs
4 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeRequisition Number: 8203Position Title: Medical Director, Medical AffairsExternal Description:About UsAt Worldwide Clinical Trials, we're a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Our company's...
-
Medical Director, Medical Affairs
4 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeRequisition Number: 8203Position Title: Medical Director, Medical AffairsExternal Description:About UsAt Worldwide Clinical Trials, we're a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Our company's...
-
Statistical Programmer
7 days ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeJob Title:Statistical Programmer - Clinical TrialsAbout Us:Worldwide Clinical Trials is a global, midsize Contract Research Organization (CRO) that pushes boundaries, innovates and invents to find cures for the world's most persistent diseases.We are a team of almost 3,000 experts, bright thinkers, dreamers and doers, working together to change the way the...
-
Medical Director, Medical Affairs Leader
3 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeRequisition Number: 8203Position Title: Medical Director, Medical AffairsExternal Description:Our Mission:At Worldwide Clinical Trials, we are dedicated to advancing new medications from discovery to reality. Our team of experts applies a scientific heritage and therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases to...
-
Medical Director, Medical Affairs Leader
3 weeks ago
London, Greater London, United Kingdom Worldwide Clinical Trials Full timeRequisition Number: 8203Position Title: Medical Director, Medical AffairsExternal Description:Our Mission:At Worldwide Clinical Trials, we're dedicated to advancing new medications from discovery to reality. Our team of 3,000+ professionals spans 60+ countries, united in our cause to improve patient lives through innovative therapies.Our Expertise:We...
-
Principal Medical Writer, Regulatory
4 weeks ago
London, Greater London, United Kingdom BioMarin Pharmaceutical Inc. Full timeJob Title: Principal Medical Writer, RegulatoryAt BioMarin Pharmaceutical Inc., we are seeking a highly skilled and experienced Principal Medical Writer, Regulatory to join our team. As a key member of our Regulatory Affairs department, you will be responsible for creating high-quality, regulatory-grade documents that support the development and approval of...
-
Principal Medical Writer, Regulatory
4 weeks ago
London, Greater London, United Kingdom BioMarin Pharmaceutical Inc. Full timeJob Title: Principal Medical Writer, RegulatoryAt BioMarin Pharmaceutical Inc., we are seeking a highly skilled and experienced Principal Medical Writer, Regulatory to join our team. As a key member of our Regulatory Affairs department, you will be responsible for creating high-quality, regulatory-grade documents that support the development and approval of...
Clinical Trials Medical Writer
2 months ago
We are seeking a skilled Medical Writer to join our team at SML Medical Supplies Inc. As a Medical Writer, you will play a crucial role in creating high-quality, scientifically sound content for our clients.
Key Responsibilities:- Develop a deep understanding of assigned therapy areas and stay up-to-date with emerging trends and advances in the field.
- Write well-crafted, scientifically accurate content that meets client needs and expectations.
- Collaborate with clients to ensure content meets their requirements.
- Provide research and content support for new business initiatives as needed.
- Ensure compliance with relevant codes of practice in content development.
- PhD in the life sciences.
- Transferable experience from academia or a non-medical communications environment, or < 1 year of medical writing experience in a medical communications agency or in-house pharma med comms team.
- Ability to write compelling medically and/or scientifically oriented content.
- Confident verbal communication around medical/scientific topics.
- Opportunity to work on a wide range of projects and develop your skills.
- Collaborative and dynamic work environment.
- Professional development opportunities.
- Flexible working arrangements.
