Sjukhusfysiker - Lediga jobb

Göteborgs universitet möter samhällets utmaningar med mångsidig kunskap. 58 000 studenter och 6800 medarbetare gör universitetet till en stor och inspirerande arbetsplats. Stark forskning och attraktiva utbildningar lockar forskare och studenter från hela världen. Med ny kunskap och nya perspektiv bidrar Göteborgs universitet till en bättre framtid.

Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

På Neurokemiska laboratoriet på Sektionen för psykiatri och neurokemi bedrivs medicinsk neurokemisk forskning med inriktning att förstå patofysiologin vid Alzheimers sjukdom och andra neurodegenerativa sjukdomar. Ett viktigt mål är att identifiera proteinförändringar kopplade till patofysiologin av humana sjukdomar, så kallade biokemiska markörer, vilka kan användas till att förstå sjukdomsmekanismer, för diagnostik och för att följa effekten av läkemedel hos människor.

Sektionen för psykiatri och neurokemi, söker nu en postdoktor för forskning kring identifiering och utveckling av biomarkörer för neurodegenerativa sjukdomar i ryggvätska och blod genom LC-MS-baserad proteomik och masspektrometri med isotoputspädning.

Ämne

Neurokemi med inriktning mot proteomik och biomarkörer 

Ämnesbeskrivning

Neurodegenerativa sjukdomar, i synnerhet demens, blir allt vanligare i takt med att befolkningen åldras. De kognitiva tester som idag används inom demensdiagnostik är ofta för trubbiga för att upptäcka lindrig kognitiv svikt eller för att särskilja mellan olika neurodegenerativa sjukdomar. Även om etablerade biomarkörer i cerebrospinalvätska (CSV), och på senare tid blodbaserade biomarkörer, finns för Alzheimers sjukdom (AD) och rutinmässigt används i diagnostiken, saknas sådana markörer fortfarande för andra tillstånd. Således behöver vi nya markörer som speglar olika sjukdomsmekanismer för att kunna ställa en tidig och säker diagnos.

Arbetsuppgifter

I anställningen ingår att utföra masspektrometribaserad proteomikanalys av cerebrospinalvätska och plasma med hjälp av tandem mass tag (TMT)-tekniken och data-independent analysis (DIA) i kohorter bestående av patienter med olika neurodegenerativa sjukdomar, såsom Alzheimers sjukdom, frontotemporal demens, amyotrofisk lateral skleros och parkinsonsjukdomar. Syftet är att identifiera proteinförändringar associerade med sjukdomarnas underliggande patologiska processer. 

Vidare ingår utveckling av riktade analysmetoder för utvalda kandidatbiomarkörer med hjälp av masspektrometri med isotoputspädning (IDMS). Anställningen är även kopplad till ett projekt som syftar till att utveckla en referensmetod för biomarkören neurofilament light chain (NfL) i plasma.

Arbetsuppgifterna omfattar provpreparation, LC–MS-analys, databearbetning och statistisk analys. I anställningen ingår även administrativa uppgifter såsom sammanställning, dokumentation och rapportering av resultat. 

Behörighet

Behörighet för anställning som lärare regleras i Högskoleförordningen 4 Kap och Göteborgs universitets anställningsordning. 

Behörig att anställas som postdoktor är den som har avlagt doktorsexamen, konstnärlig doktorsexamen eller som har en utländsk examen som bedöms motsvara doktorsexamen. Detta behörighetskrav ska vara uppfyllt senast vid tidpunkten då anställningsbeslutet fattas.

I första hand bör den komma i fråga som har avlagt examen högst tre år före ansökningstidens utgång. Även den som avlagt examen tidigare bör komma i fråga i första hand, om det finns särskilda skäl. Med särskilda skäl avses ledighet på grund av sjukdom, föräldraledighet, förtroendeuppdrag inom fackliga organisationer, tjänstgöring inom totalförsvaret, eller andra liknande omständigheter samt klinisk tjänstgöring eller för ämnesområdet relevant tjänstgöring/uppdrag.

Behörig att anställas som postdoktor för denna anställning är den som innehar doktorsexamen inom biomedicin, neurokemi, neuroproteomik eller relaterade områden.

Bedömningsgrund

Den sökande skall ha forskningserfarenhet inom området proteomik, biomarkörer och neurologiska sjukdomar. Kunskap och erfarenhet av högupplösande masspektrometri och bioinformatisk analys av proteomikdata är meriterande. Övriga önskvärda kvalifikationer är en god förmåga att självständigt bearbeta data och att koordinera projekt och ha kontakter med samarbetspartners. Stor vikt kommer också att läggas vid personlig lämplighet.

Anställning

Anställningen är en tidsbegränsad anställning i 2 år, 100% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse.  

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta forskare Johan Gobom, tfn: +46 730 229 028, e-post: mailto:johan.gobom@neuro.gu.se

Ansvarig chef är professor/sektionschef Henrik Zetterberg, tfn: +46 768 672 647, e-post: mailto:henrik.zetterberg@clinchem.gu.se

Ansökningshandlingar skickas inte till kontaktpersonerna.

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag. 

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2026-07-17

Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten. Universitetet tillämpar individuell lönesättning. Enligt Riksarkivets föreskrifter är universitetet skyldigt att förvara ansökningshandlingar i två år efter tillsättningsbeslutet. Om du som sökande till en anställning särskilt begär tillbaka dina handlingar återsänds de när de två åren har förflutit, i annat fall kommer de att gallras ut. Till bemannings- och rekryteringsföretag och till dig som är försäljare: Göteborgs universitet anlitar upphandlad annonsbyrå i samband med rekrytering av personal. Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av jobbannonser.

Göteborgs universitet möter samhällets utmaningar med mångsidig kunskap. 58 000 studenter och 6800 medarbetare gör universitetet till en stor och inspirerande arbetsplats. Stark forskning och attraktiva utbildningar lockar forskare och studenter från hela världen. Med ny kunskap och nya perspektiv bidrar Göteborgs universitet till en bättre framtid.

Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

På Neurokemiska laboratoriet på Sektionen för psykiatri och neurokemi bedrivs medicinsk neurokemisk forskning med inriktning att förstå patofysiologin vid Alzheimers sjukdom och andra neurodegenerativa sjukdomar. Ett viktigt mål är att identifiera proteinförändringar kopplade till patofysiologin av humana sjukdomar, så kallade biokemiska markörer, vilka kan användas till att förstå sjukdomsmekanismer, för diagnostik och för att följa effekten av läkemedel hos människor.

Sektionen för psykiatri och neurokemi, söker nu en postdoktor för forskning kring identifiering och utveckling av biomarkörer för neurodegenerativa sjukdomar i ryggvätska och blod genom LC-MS-baserad proteomik och masspektrometri med isotoputspädning.

Ämne

Neurokemi med inriktning mot proteomik och biomarkörer 

Ämnesbeskrivning

Neurodegenerativa sjukdomar, i synnerhet demens, blir allt vanligare i takt med att befolkningen åldras. De kognitiva tester som idag används inom demensdiagnostik är ofta för trubbiga för att upptäcka lindrig kognitiv svikt eller för att särskilja mellan olika neurodegenerativa sjukdomar. Även om etablerade biomarkörer i cerebrospinalvätska (CSV), och på senare tid blodbaserade biomarkörer, finns för Alzheimers sjukdom (AD) och rutinmässigt används i diagnostiken, saknas sådana markörer fortfarande för andra tillstånd. Således behöver vi nya markörer som speglar olika sjukdomsmekanismer för att kunna ställa en tidig och säker diagnos.

Arbetsuppgifter

I anställningen ingår att utföra masspektrometribaserad proteomikanalys av cerebrospinalvätska och plasma med hjälp av tandem mass tag (TMT)-tekniken och data-independent analysis (DIA) i kohorter bestående av patienter med olika neurodegenerativa sjukdomar, såsom Alzheimers sjukdom, frontotemporal demens, amyotrofisk lateral skleros och parkinsonsjukdomar. Syftet är att identifiera proteinförändringar associerade med sjukdomarnas underliggande patologiska processer. 

Vidare ingår utveckling av riktade analysmetoder för utvalda kandidatbiomarkörer med hjälp av masspektrometri med isotoputspädning (IDMS). Anställningen är även kopplad till ett projekt som syftar till att utveckla en referensmetod för biomarkören neurofilament light chain (NfL) i plasma.

Arbetsuppgifterna omfattar provpreparation, LC–MS-analys, databearbetning och statistisk analys. I anställningen ingår även administrativa uppgifter såsom sammanställning, dokumentation och rapportering av resultat. 

Behörighet

Behörighet för anställning som lärare regleras i Högskoleförordningen 4 Kap och Göteborgs universitets anställningsordning. 

Behörig att anställas som postdoktor är den som har avlagt doktorsexamen, konstnärlig doktorsexamen eller som har en utländsk examen som bedöms motsvara doktorsexamen. Detta behörighetskrav ska vara uppfyllt senast vid tidpunkten då anställningsbeslutet fattas.

I första hand bör den komma i fråga som har avlagt examen högst tre år före ansökningstidens utgång. Även den som avlagt examen tidigare bör komma i fråga i första hand, om det finns särskilda skäl. Med särskilda skäl avses ledighet på grund av sjukdom, föräldraledighet, förtroendeuppdrag inom fackliga organisationer, tjänstgöring inom totalförsvaret, eller andra liknande omständigheter samt klinisk tjänstgöring eller för ämnesområdet relevant tjänstgöring/uppdrag.

Behörig att anställas som postdoktor för denna anställning är den som innehar doktorsexamen inom biomedicin, neurokemi, neuroproteomik eller relaterade områden.

Bedömningsgrund

Den sökande skall ha forskningserfarenhet inom området proteomik, biomarkörer och neurologiska sjukdomar. Kunskap och erfarenhet av högupplösande masspektrometri och bioinformatisk analys av proteomikdata är meriterande. Övriga önskvärda kvalifikationer är en god förmåga att självständigt bearbeta data och att koordinera projekt och ha kontakter med samarbetspartners. Stor vikt kommer också att läggas vid personlig lämplighet.

Anställning

Anställningen är en tidsbegränsad anställning i 2 år, 100% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse.  

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta forskare Johan Gobom, tfn: +46 730 229 028, e-post: mailto:johan.gobom@neuro.gu.se

Ansvarig chef är professor/sektionschef Henrik Zetterberg, tfn: +46 768 672 647, e-post: mailto:henrik.zetterberg@clinchem.gu.se

Ansökningshandlingar skickas inte till kontaktpersonerna.

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag. 

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2026-07-17

Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten. Universitetet tillämpar individuell lönesättning. Enligt Riksarkivets föreskrifter är universitetet skyldigt att förvara ansökningshandlingar i två år efter tillsättningsbeslutet. Om du som sökande till en anställning särskilt begär tillbaka dina handlingar återsänds de när de två åren har förflutit, i annat fall kommer de att gallras ut. Till bemannings- och rekryteringsföretag och till dig som är försäljare: Göteborgs universitet anlitar upphandlad annonsbyrå i samband med rekrytering av personal. Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av jobbannonser.

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.

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.

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.

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.

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.