20 Jobs für Pharmaceutical Writing in Berlin
Stellenangebote Pharmaceutical Writing in Berlin Jobs
Job am 10.03.2026 bei StepStone gefunden
Novanta
• Berlin
[. .. ] Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation Plans and Reports (PRISMA PICO analysis) to assess the safety and performance, in accordance with applicable standards Strong attention to detail and maintaining accurate and [. .. ] ISO 14155) is required Knowledge of Clinical indication and application in Minimally Invasive Surgery is a plus Expert knowledge and experience in Medical Device/ Clinical investigation (ISO 14115) and/or pharmaceutical industries is a plus Fluent written and spoken English (at least C1) is required; German language skills is a plus Open and competent attitude when working with your stakeholders IT affinity and proficiency with the MS Office package Familiarity with AI tools is a plus Travel Requirements Travel by public [. .. ]
Job am 21.02.2026 bei StepStone gefunden
Novanta
Medical Affairs Manager (m/f/d)
• Berlin
[. .. ] Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation Plans and Reports (PRISMA PICO analysis) to assess the safety and performance, in accordance with applicable standards Strong attention to detail and maintaining accurate and [. .. ] ISO 14155) is required Knowledge of Clinical indication and application in Minimally Invasive Surgery is a plus Expert knowledge and experience in Medical Device/ Clinical investigation (ISO 14115) and/or pharmaceutical industries is a plus Fluent written and spoken English (at least C1) is required; German language skills is a plus Open and competent attitude when working with your stakeholders IT affinity and proficiency with the MS Office package Familiarity with AI tools is a plus Travel Requirements Travel by public [. .. ]
Job gestern bei Jobleads gefunden
• Berlin
[. .. ] Berlin/ Porto/ Riga or remote (Germany/ Portugal/ Latvia) Starting: at the next possible date LETS SPILL THE TEA ABOUT US: THE FORCE builds companies for companies in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the healthcare and pharmaceutical sector. We encourage work in flexible surroundings and as a diverse group when it comes to gender, nationality, religion, and ways of working. This unique culture is aimed at integrating employees and partners seamlessly into one organisation. Likewise, this organization shall easily adapt to customer organisations. Our unique way of [. .. ] ICH-GCP, regulatory requirements, and sponsor standards. Your literature research and scientific analysis dont leave a bitter aftertaste. You brew up study reports, scientific publications, and presentations. You tend to writing Clinical Study Reports (CSR) as well as to scientific writing/ reporting for publications and congress posters. You keep the pot boiling when it comes to the maintenance of accurate trial documentation and regulatory files. You pour your support into teaching activities and educational programs. You set a high bar for [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
(Senior) Principal-Clinical Outcome Assessment Science-Multiple locations in Europe-Hybri. . .
• Berlin
[. .. ] project delivery. This role brings deep expertise in COA measurement science to differentiate client solutions through expert-driven, highly insightful endpoint strategies. The role acts as a trusted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] advisor to pharmaceutical and biotechnology sponsors and represents IQVIA as an external scientific thought leader while ensuring internal scientific quality and best practices. Key responsibilities include: Client Strategy Leadership Scientific Differentiation Develop COA endpoint strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects. Bring senior COA expertise [. .. ] types (PRO, Obs RO, Clin RO, Perf O) and their application in clinical research. Extensive experience developing COA endpoint strategies across multiple therapeutic areas. Hands-on experience developing new COA instruments, including item writing and qualitative validation. Strong experience supporting FDA-facing endpoint strategy and regulatory interactions. Proven ability to lead, mentor, and oversee multidisciplinary scientific teams. Excellent scientific writing, presentation, and stakeholder engagement skills. Advanced degree (Ph D, MD, Pharm D, Dr PH, MSc) in a relevant scientific discipline strongly preferred. Strong publication record and recognized [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Giengen an der Brenz, Baden- Württemberg
[. .. ] Berlin/ Porto/ Riga or remote (Germany/ Portugal/ Latvia) Starting: at the next possible date Lets Spill The Tea About Us THE FORCE builds companies for companies in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the healthcare and pharmaceutical sector. We encourage work in flexible surroundings and as a diverse group when it comes to gender, nationality, religion, and ways of working. This unique culture is aimed at integrating employees and partners seamlessly into one organisation. Likewise, this organization shall easily adapt to customer organisations. Our unique way of [. .. ] ICH-GCP, regulatory requirements, and sponsor standards. Your literature research and scientific analysis dont leave a bitter aftertaste. You brew up study reports, scientific publications, and presentations. You tend to writing Clinical Study Reports (CSR) as well as to scientific writing/ reporting for publications and congress posters. You keep the pot boiling when it comes to the maintenance of accurate trial documentation and regulatory files. You pour your support into teaching activities and educational programs. You set a high bar for [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Senior Data Analyst
• Berlin
[. .. ] SQL and Python Experience in data storage and processing on cloud platforms such as AWS, GCP, or Azure Strong problem-solving skills and experience working with cross-functional teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Experience writing process documentation and data collection guidelines Nice to Have University degree in medicine or life sciences Understanding of healthcare, life sciences, or pharmaceutical industry data Experience with data visualization tools to create dashboards and reports Understanding of data engineering concepts (ETL, data pipelines) Experience with workflow automation tools such as Apache Airflow Experience working in an Agile or product-driven environment Familiarity with data privacy and compliance regulations (e. g. GDPR, HIPAA) Perks [. .. ]
Job am 24.03.2026 bei Jobleads gefunden
• Berlin
[. .. ] Heidenheim a. d. Brenz, Berlin, Porto, Riga, or remote (Germany/ Portugal/ Latvia) Starting: at the next possible date Your New Waters The FORCE builds companies for companies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in the healthcare, pharmaceutical, and medical devices sector. We encourage work in a flexible surrounding and as a diverse group when it comes to gender, nationality, religion, and ways of working. This unique culture is aimed to integrate employees and partners seamlessly into one organization. Likewise, this organization shall easily adapt to customer organizations. [. .. ] are in the swim in at least one area of our widely span activities from MAA strategy to life-cycle measures or local regulatory activities, e. g. technical or medical writing, life-cycle management, submission and procedure management, labelling. Your experience allows you to handle regulatory submissions (including e CTD publishing) swimmingly. Global and/or European projects arent unchartered waters to you. You bring along an ocean of knowledge when it comes to regulatory procedures and guidelines in the EU and beyond. [. .. ]
Job am 17.03.2026 bei Jobleads gefunden
Medical Affairs Lead
• Berlin
Führungs-/ Leitungspositionen
[. .. ] AI-powered tools at the convergence of medical imaging, radioligand therapy, and artificial intelligence. Starting with prostate cancer and expanding across oncology, we partner with world-leading medical institutions [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and pharmaceutical companies across the US, Europe, and Australia to bring precision oncology into everyday clinical practice. Our mission is to enhance diagnostic precision and expand access to expert-level cancer care, improving patient outcomes worldwide. Were venture-backed, early-stage, and building a team that blends deep clinical expertise with engineering [. .. ] Bring Bachelors or advanced degree in Medical Imaging, Medical Science, Life Sciences, or related field 3+ years of experience in medical affairs, medical science liaison, or clinical communications Strong scientific writing and data presentation skills; experience with peer-reviewed publications Experience building relationships with KOLs and clinical research communities Experience managing or coordinating clinical annotation, labeling, or data review teams Excellent communication skills; able to bridge clinical, product, and commercial audiences Bonus Points Experience in nuclear medicine, PET/ CT imaging, or [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Medical Affairs Manager Medical Devices (m/f/d)
• Berlin
[. .. ] Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation Plans and Reports (PRISMA PICO analysis) to assess the safety and performance, in accordance with applicable standards Strong attention to detail and maintaining accurate and [. .. ] ISO 14155) is required Knowledge of Clinical indication and application in Minimally Invasive Surgery is a plus Expert knowledge and experience in Medical Device/ Clinical investigation (ISO 14115) and/or pharmaceutical industries is a plus Fluent written and spoken English (at least C1) is required; German language skills is a plus Open and competent attitude when working with your stakeholders IT affinity and proficiency with the MS Office package Familiarity with AI tools is a plus Travel Requirements Travel by public [. .. ]
Job am 22.02.2026 bei Jobleads gefunden
Senior Medical Writer
• Berlin
[. .. ] content, patient narratives, and medical information engagement plans. Support the creation of visual content through effective data visualization techniques and contribute to innovative out of the box [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] solutions for medical writing projects. Ensure all materials align with client requirements, style guides, templates, preferences, and CACTUS internal SOPs, updating documents consistently to keep all content current and compliant. Perform as a document specialist, provide intellectual input across document types, and contribute to making cuttingedge research accessible to specific audiences as appropriate, by [. .. ] strong scientific writing skills. Ph D in medical, life or health sciences, or pharmacy or Masters degree in life sciences At least 3 years experience as a medical writer within the pharmaceutical industry, ideally within a medical communications agency Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Literature reviewing and evaluation capabilities. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Ability to multitask and work [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
• Berlin
[. .. ] Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation Plans and Reports (PRISMA PICO analysis) to assess the safety and performance, in accordance with applicable standards Strong attention to detail and maintaining accurate and [. .. ] ISO 14155) is required Knowledge of Clinical indication and application in Minimally Invasive Surgery is a plus Expert knowledge and experience in Medical Device/ Clinical investigation (ISO 14115) and/or pharmaceutical industries is a plus Fluent written and spoken English (at least C1) is required; German language skills is a plus Open and competent attitude when working with your stakeholders IT affinity and proficiency with the MS Office package Familiarity with AI tools is a plus Travel Requirements Travel by public [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
Medical Affairs Manager (m/f/d)
• Berlin
[. .. ] Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation Plans and Reports (PRISMA PICO analysis) to assess the safety and performance, in accordance with applicable standards Strong attention to detail and maintaining accurate and [. .. ] ISO 14155) is required Knowledge of Clinical indication and application in Minimally Invasive Surgery is a plus Expert knowledge and experience in Medical Device/ Clinical investigation (ISO 14115) and/or pharmaceutical industries is a plus Fluent written and spoken English (at least C1) is required; German language skills is a plus Open and competent attitude when working with your stakeholders IT affinity and proficiency with the MS Office package Familiarity with AI tools is a plus Travel Requirements Travel by public [. .. ]
Job am 18.02.2026 bei Jobleads gefunden
• Berlin
[. .. ] an attorney in a large law firm, biopharmaceutical company and/or technology company practicing law related to life sciences/ healthcare, digital health or technology Experience counseling on EMA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulation of pharmaceutical and device products, including mobile medical applications, connected devices, clinical decision support software and other diagnostic solutions, combination and companion products is strongly preferred Strong interpersonal communications, research and writing skills Highly developed ability to identify and advise on diverse legal, business, regulatory and compliance issues on a timely basis and to work independently and in a highly collaborative, cross-functional team Solid transactional and negotiating experience Common sense and good practical business judgment Fluency in English German language skills [. .. ]
Job am 18.12.2025 bei Jobleads gefunden
Quality Control Chemist (m/f/d)
• Berlin
[. .. ] Prepare test records, participate in drafting analysis reports, stability reports and Certificates of Analysis Participate in development of analytical procedures for the analysis of raw materials, in-process [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] samples and pharmaceutical products Perform instrumental analysis to assist in method development Research literature and pharmacopeia for methods when necessary Assist other members of the QC team with method development tasks Ensure GMP-compliant maintenance and qualification of QC equipment Organize and carry out equipment qualification as requested by the QC Manager, ensuring [. .. ] proteins and/or synthetic polymers Strong analytical interpretation skills General technical user knowledge in analytical instrumentation Intermediate to good English and German language competency (level B2/ C1) in speech and writing Selfmotivated, wellorganized, and proactive learner Ability to work independently in a structured manner Ability and willingness to train and instruct coworkers in newly developed testing methods Team player especially concerning work and lab organisation About us Biosynth is an innovative life sciences reagents, custom synthesis and manufacturing services company headquartered [. .. ]
Job gestern bei Neuvoo gefunden
Pharmtrace klinische Entwicklung GmbH
• Berlin
Homeoffice möglich
Betriebliche Altersvorsorge Jobticket
[. .. ] your sleeves and dive in deep into daily admin tasks: you ensure that every aspect of your project gets done, incl. detailed and assiduous documentation you can [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] use your academic writing/ reading/ analysis skills with us You are pro-active and empathetic in your communication with your colleagues: we work together as a team on all projects and ensure the best possible outcome for our clients and our company as a whole by regular, empathetic and pro-active communication via MS [. .. ] regulatory authorities, selection and qualification of hospital departments as trial sites, monitoring, safety, clinical image data management, statistical analysis and study report writing. Our clients are small and medium-sized pharmaceutical companies based in Europe, North America and Australasia. Our company headquarters are in Berlin, Germany, and Philadelphia, USA. 87749813 [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
IQVIA
(Senior) Principal-Clinical Outcome Assessment Science-Multiple locations in Europe-Hybrid/Home-based
• Berlin
[. .. ] engagement and project delivery. This role brings deepexpertisein COA measurement science to differentiate client solutions through expert-driven, highly insightful endpoint strategies. The role acts as a trusted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] advisor to pharmaceutical and biotechnology sponsors and represents IQVIA as an external scientific thought leader while ensuring internal scientific quality and best practices. Key responsibilities include: Client Strategy Leadership Scientific Differentiation Develop COA endpoint strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects. Bring senior COA expertise [. .. ] types (PRO, Obs RO, Clin RO, Perf O) and their application in clinical research. Extensive experience developing COA endpoint strategies across multiple therapeutic areas. Hands-on experience developing new COA instruments, including item writing and qualitative validation. Strong experience supporting FDA-facing endpoint strategy and regulatory interactions. Proven ability to lead, mentor, and oversee multidisciplinary scientific teams. Excellent scientific writing, presentation, and stakeholder engagement skills. Advanced degree (Ph D, MD, Pharm D, Dr PH, MSc) in a relevant scientific discipline strongly preferred. Strong publication record and recognized [. .. ]
Job am 23.03.2026 bei Neuvoo gefunden
Veeva Systems
• Berlin
[. .. ] SQL and Python Experience in data storage and processing on cloud platforms such as AWS, GCP, or Azure Strong problem-solving skills and experience working with cross-functional teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Experience writing process documentation and data collection guidelines Nice to Have University degree in medicine or life sciences Understanding of healthcare, life sciences, or pharmaceutical industry data Experience with data visualization tools to create dashboards and reports Understanding of data engineering concepts (ETL, data pipelines) Experience with workflow automation tools such as Apache Airflow Experience working in an Agile or product-driven environment Familiarity with data privacy and compliance regulations (e. g. GDPR, HIPAA) Perks [. .. ]
Job am 15.03.2026 bei Neuvoo gefunden
Nucs AI
Medical Affairs Lead
• Berlin
Führungs-/ Leitungspositionen
[. .. ] AI-powered tools at the convergence of medical imaging, radioligand therapy, and artificial intelligence. Starting with prostate cancer and expanding across oncology, we partner with world-leading medical institutions [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and pharmaceutical companies across the US, Europe, and Australia to bring precision oncology into everyday clinical practice. Our mission is to enhance diagnostic precision and expand access to expert-level cancer care, improving patient outcomes worldwide. Were venture-backed, early-stage, and building a team that blends deep clinical expertise with engineering [. .. ] Bring Bachelors or advanced degree in Medical Imaging, Medical Science, Life Sciences, or related field 3+ years of experience in medical affairs, medical science liaison, or clinical communications Strong scientific writing and data presentation skills; experience with peer-reviewed publications Experience building relationships with KOLs and clinical research communities Experience managing or coordinating clinical annotation, labeling, or data review teams Excellent communication skills; able to bridge clinical, product, and commercial audiences Bonus Points Experience in nuclear medicine, PET/ CT imaging, or [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
Pro Pharma Group
• Berlin
For the past 20 years, Pro Pharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and
pharmaceutical organizations of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the worlds largest RCO (Research Consulting Organization) , Pro Pharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality [. .. ] contact centers around the world, we provide customizable medical information services to meet the needs of companies of all sizes. Whether you need adverse event intake and follow-up, medical writing and content management solutions, promotional review, or other extended medical information services, our team of medical information specialists have the knowledge and experience to effectively support your needs. You can find out more about our Medical Information department and what they do here: The Day-to-day Answering technical questions [. .. ]
Neu Job heute bei Jooble gefunden
Indegene
Medical Copywriting Manager Germany
• Berlin
[. .. ] is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Key qualifications include [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] :-Experience with pharmaceutical brands-Knowledge of pharma regulations-Strong understanding of therapies and patient needs-Background in medical promotional marketing-Agency experience-Proficiency in German and English at C1 level or fluent-Candidates must be located in Germany Who are you? We are looking for a talented professional with medical copywriting skills that also [. .. ] ensuring that content development activities are supported by authentic and up-to-date references. -Thorough with PAAB submission and approval process including organizations internal MLR submissions. -Strong conceptual abilities, remarkable writing skills and a solid knowledge of the digital landscape-Support client engagement to act as brand partner, ensure project management and act as a liaison with the client and internal teams. -Develop and update content for various commercial assets, with a focus on omnichannel implementation on digital channels (including banner [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Writing pro Jahr?
Als Pharmaceutical Writing verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Writing Jobs in Berlin bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 20 offene Stellenanzeigen für Pharmaceutical Writing Jobs in Berlin.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Jobs in Berlin?
Aktuell suchen 8 Unternehmen nach Bewerbern für Pharmaceutical Writing Jobs in Berlin.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Stellenangebote in Berlin?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Writing Stellenangebote in Berlin:
- Novanta (2 Jobs)
- Pharmtrace klinische Entwicklung GmbH (1 Job)
- IQVIA (1 Job)
- Veeva Systems (1 Job)
- Nucs AI (1 Job)
- Pro Pharma Group (1 Job)
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs in Berlin?
Pharmaceutical Writing Jobs in Berlin gehören zum Berufsfeld Technische Dokumentation / Redaktion.
