Medical writer
CTC Clinical Trial Consultants ABSammanfattning
CTC is seeking an experienced Medical Writer to join their team in Uppsala, contributing to the development of regulatory documents for clinical trials. The role involves writing clinical study protocols and reports, coordinating quality control processes, and collaborating with cross-functional project teams. The position allows for hybrid work and is full-time, offering opportunities for professional development in a supportive environment.Jobbet i korthet
Anställningstyp
tillsvidareanstallning
Arbetstid
heltid
Förmåner
Flexible working hours.Wellness allowance.Generous vacation terms.Professional development opportunities in a knowledge-intensive environment.
Ansök senast: 2026-08-17
Publicerad: 2026-07-03
Beskrivning
Join CTC - where ambition is high and one of the goals is to strengthen the Swedish infrastructure in the Life Sciences! We are growing and are now looking for an additional Medical Writer who wants to contribute to CTC's continued journey. Are you an experienced Medical Writer (MW) who wants to use your expertise to drive CTC's development? Then this is the opportunity for you!
As a Medical Writer at CTC, you will be part of a team of four other MWs responsible for writing and quality-checking regulatory documents, primarily clinical study protocols and reports. The work alternates between individual tasks and teamwork. You will be part of various study-specific project teams responsible for initiating and managing clinical projects until the delivery of study results. These cross-functional project teams include professionals such as project managers, medical and scientific advisors, research nurses, doctors, statisticians, and more.
Main responsibilities:
To write clinical study protocols and clinical study reports in accordance with ICH E6, ICH E3, and/or ISO 14155, and coordinate the development and quality control processes of these documents, both internally and with our clients.
To write other regulatory documents and texts such as summary of results, narratives, substantial amendments and responses to authorities.
To coordinate and lead meetings, both internally and externally, and act as a point of contact for clients.
To serve as a mentor to colleagues.
Other tasks such as medical coding, writing abstracts and scientific articles, writing assignments related to safety reporting, and writing marketing documents may also be required.
We are looking for a driven and experienced Medical Writer who truly enjoys writing and formulating scientific texts. To succeed in this role, you need to have the ability to quickly and efficiently interpret, summarize, and present large amounts of data. We require you to have at least 3 years of experience in medical writing, drug development, and clinical trials.
Previous experience in consultancy work and an understanding of the customer perspective are also valued. As a person, you are communicative and enjoy collaborating with experts in various fields. You are flexible, works independently, and deliver within agreed timelines. CTC's core values: Innovation, Community, Respect, Commitment, and Professionalism resonate with you.
Required qualifications
MSc in the life sciences field.
At least 3 years of experience in medical writing, drug development, and clinical trials.
Experience in leading meetings and coordinating complex and parallel deliveries within agreed timelines.
Proficiency in using the Microsoft Office suite, especially Microsoft Word.
Excellent ability to express yourself grammatically correctly and clearly in English, both spoken and written.
Good knowledge of the Swedish language (spoken and written).
Preferred qualifications
A PhD in the life sciences field.
Experience with Phase 2-3 trials.
Experience with medical devices and/or advanced therapy medicinal products (ATMP), as well as knowledge of regulatory requirements related to these areas.
Experience in writing eCTD module 2; Clinical and Non-Clinical overview/summary, Investigator's Brochures (IBs), Annual Safety Reports (ASRs).
At CTC, you will be covered by a collective agreement and offered benefits such as flexible working hours, wellness allowance, and generous vacation terms. You will have the opportunity to work in a knowledge-intensive environment in a company with short decision-making paths, with good professional development opportunities.
The position is located at our office in Uppsala (hybrid work is possible). Full time (40 hours per week).
If you have questions, contact Marit Wangheim (Director Medical Writing) marit.wangheim@ctc-ab.se
Please submit your application no later than 17 August 2026.
CTC Clinical Trial Consultants AB is a Clinical Research Organization (CRO) with operations in Uppsala, Stockholm, Linköping, and Gothenburg.
As a CRO, we conduct clinical trials and investigations on behalf of the pharmaceutical and medtech industry and academic institutions. We offer a comprehensive full-service solution that includes all the services, activities, and deliverables required to successfully conduct a clinical trial- bringing new pharmaceuticals and products to patients. We currently conduct clinical studies across all phases of development, from Phase 0 through Phase IV.
Most of our studies are carried out at our own research clinics, although we also collaborate with external clinical sites.
We employ approximately 125 people, around half of whom work in clinical roles. Our headquarters are located in Uppsala.
As a Medical Writer at CTC, you will be part of a team of four other MWs responsible for writing and quality-checking regulatory documents, primarily clinical study protocols and reports. The work alternates between individual tasks and teamwork. You will be part of various study-specific project teams responsible for initiating and managing clinical projects until the delivery of study results. These cross-functional project teams include professionals such as project managers, medical and scientific advisors, research nurses, doctors, statisticians, and more.
Main responsibilities:
To write clinical study protocols and clinical study reports in accordance with ICH E6, ICH E3, and/or ISO 14155, and coordinate the development and quality control processes of these documents, both internally and with our clients.
To write other regulatory documents and texts such as summary of results, narratives, substantial amendments and responses to authorities.
To coordinate and lead meetings, both internally and externally, and act as a point of contact for clients.
To serve as a mentor to colleagues.
Other tasks such as medical coding, writing abstracts and scientific articles, writing assignments related to safety reporting, and writing marketing documents may also be required.
We are looking for a driven and experienced Medical Writer who truly enjoys writing and formulating scientific texts. To succeed in this role, you need to have the ability to quickly and efficiently interpret, summarize, and present large amounts of data. We require you to have at least 3 years of experience in medical writing, drug development, and clinical trials.
Previous experience in consultancy work and an understanding of the customer perspective are also valued. As a person, you are communicative and enjoy collaborating with experts in various fields. You are flexible, works independently, and deliver within agreed timelines. CTC's core values: Innovation, Community, Respect, Commitment, and Professionalism resonate with you.
Required qualifications
MSc in the life sciences field.
At least 3 years of experience in medical writing, drug development, and clinical trials.
Experience in leading meetings and coordinating complex and parallel deliveries within agreed timelines.
Proficiency in using the Microsoft Office suite, especially Microsoft Word.
Excellent ability to express yourself grammatically correctly and clearly in English, both spoken and written.
Good knowledge of the Swedish language (spoken and written).
Preferred qualifications
A PhD in the life sciences field.
Experience with Phase 2-3 trials.
Experience with medical devices and/or advanced therapy medicinal products (ATMP), as well as knowledge of regulatory requirements related to these areas.
Experience in writing eCTD module 2; Clinical and Non-Clinical overview/summary, Investigator's Brochures (IBs), Annual Safety Reports (ASRs).
At CTC, you will be covered by a collective agreement and offered benefits such as flexible working hours, wellness allowance, and generous vacation terms. You will have the opportunity to work in a knowledge-intensive environment in a company with short decision-making paths, with good professional development opportunities.
The position is located at our office in Uppsala (hybrid work is possible). Full time (40 hours per week).
If you have questions, contact Marit Wangheim (Director Medical Writing) marit.wangheim@ctc-ab.se
Please submit your application no later than 17 August 2026.
CTC Clinical Trial Consultants AB is a Clinical Research Organization (CRO) with operations in Uppsala, Stockholm, Linköping, and Gothenburg.
As a CRO, we conduct clinical trials and investigations on behalf of the pharmaceutical and medtech industry and academic institutions. We offer a comprehensive full-service solution that includes all the services, activities, and deliverables required to successfully conduct a clinical trial- bringing new pharmaceuticals and products to patients. We currently conduct clinical studies across all phases of development, from Phase 0 through Phase IV.
Most of our studies are carried out at our own research clinics, although we also collaborate with external clinical sites.
We employ approximately 125 people, around half of whom work in clinical roles. Our headquarters are located in Uppsala.
Ansök till tjänsten
Medical writer
OM FÖRETAGET
CTC Clinical Trial Consultants AB
