77 Jobs für Regulatory Writing in Berlin
Stellenangebote Regulatory Writing in Berlin Jobs
Job am 10.03.2026 bei StepStone gefunden
Novanta
• Berlin
Teilzeit Werkstudenten
[. .. ] with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Job Summary As a Material Compliance Intern, you will support the Material [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Compliance team in regulatory compliance activities by reviewing documentation, supporting system and datarelated tasks, and assisting with material compliance declarations in an international environment. Position Details Primary Responsibilities Be part of the Material Compliance team and actively support regulatory and operational compliance activities across the product lifecycle. Take ownership of compliance request coordination and [. .. ] data preparation and documentation. Assist in maintaining compliance databases, substance inventories and legal registers for chemical and product regulations. Additional tasks may be assigned by the manager verbally or in writing Required Experience, Education, Skills, Training and Competencies Enrolled student (Bachelors or Masters) in engineering, natural sciences, environmental sciences or a comparable field. Interest in material compliance, chemical regulations or product compliance topics. Strong knowledge of Microsoft Office, including a high proficiency in Excel; knowledge in Power BI preferred. Structured, detail-[. .. ]
Job am 10.03.2026 bei StepStone gefunden
Novanta
Medical Affairs Manager Medical Devices (m/f/d)
• Berlin
[. .. ] procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/ MEDDEV. Primary Responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR) , Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report) , and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) [. .. ] 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 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 [. .. ]
Job am 21.02.2026 bei StepStone gefunden
Novanta
• Berlin
[. .. ] procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/ MEDDEV. Primary Responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR) , Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report) , and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) [. .. ] 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 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 [. .. ]
Job am 14.02.2026 bei StepStone gefunden
Novanta
Post Market Surveillance (PMS) Specialist Medical Devices (m/f/d)
• Berlin
[. .. ] recalls/ FSCAs and/or corrective actions. Evaluation of adverse events based on the event description and medical device investigation results Provision of a decision on reporting obligations based [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on international regulatory requirements Reporting of adverse events in line with country-specific requirements Search and evaluation of vigilance data for medical devices using country-specific databases Support with risk analysis and assessment of benefit-risk-ratio Provision of a significant input in Health-Risk Assessments Provision of a decision on recall/ FSCA [. .. ] vigilance database management and the evaluation of vigilance data, focusing on the benefit-risk ratio, required Experience in literature search and review required as well as knowledge of regulatory medical writing General QMS knowledge Open and competent attitude when working with your stakeholders Fluent written and spoken English, German would be a plus Ability to coordinate complex workflows Structured and systematic working approach High-quality documentation skills Travel Requirements Attendance on conferences, conferences and trade shows Willingness to travel to all [. .. ]
Job am 22.03.2026 bei Jobleads gefunden
• Berlin, Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] the maintenance of our current product portfolio. This role requires a blend of quantitative and qualitative analysis, exceptional communication skills, and a proactive approach to staying current [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with market and regulatory developments. You will be responsible for monitoring your own portfolio of ratings, as well as assigning new ratings as Scopes coverage grows. You will be the subject matter expert on your coverage, representing the team and Scope visvis issuers, investors, and the media and regularly produce research to strengthen Scopes [. .. ] estate) among others Willingness to take responsibility with an entrepreneurial attitude Independent thinker with strong analytical and problemsolving skills Multicultural, collaborative, selfstarter, versatile, inquisitive and detailoriented personality Experience in research writing with strong written and oral communication skills Team player with excellent interpersonal skills Ability to meet deadlines and motivate others to do the same Strong MS Office (Word, Excel, Power Point) computer skills Fluency in at least one major European language (English and/or French preferred) in addition to German [. .. ]
Neu Job heute bei Jobleads gefunden
Senior Data Engineer (m/f/d)
• Berlin
[. .. ] job is not for you, if You need a welldefined scope handed to you on day one. You prefer working in isolation and shipping quietly. You think [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data engineer means writing SQL and waiting for requirements. You need a large team around you to be effective. Youre not comfortable working under bankinggrade regulatory scrutiny. Hard Requirements 3+ years building data infrastructure with tooling such as AWS/ GCP/ Azure, Snowflake/ Click House/ Redshift, orchestration, pipelines. Experience in a heavily regulated industry banking, fintech, payments. You know what it means to build data systems under regulatory scrutiny. Based in Berlin or willing to relocate this [. .. ]
Job gestern bei Jobleads gefunden
• Berlin
[. .. ] research, ideally in digital health or medical devices. Strong statistical and data analysis skills (e. g. R, Python) and a solid understanding of clinical methodology. Proven track [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] record in scientific writing, grant applications, and regulatory submissions. Experience with Sa MD, ISO 14155, MDR, and CDS systems is a strong plus. Hands-on experience with Electronic Data Capture (EDC) and real-world evidence projects. Fluency in English and German, both written and spoken. A strategic thinker who can translate clinical needs into product design and business impact. [. .. ]
Job gestern bei Jobleads gefunden
Medical Affairs Manager
• Berlin
[. .. ] YOU: You add your ingredients to the planning, coordination, and execution of medical and scientific research projects, including clinical trials. You ensure the recipes for Good Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Practice (GCP) and regulatory requirements are followed. You assist in study documentation, data collection, and data management. You become a regular in coordinating communication between investigators, sponsors, CROs, and study teams, as well as in aligning 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 2 Tagen bei Jobleads gefunden
• Berlin
Sabbaticals
[. .. ] youll be the architect of Personios total rewards philosophy-designing compensation and equity programs that attract and retain top talent across Europe. This isnt about running a playbook; [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] its about writing one. Youll own our equity strategy end-to-end, partner with leadership on critical decisions, and build scalable frameworks that support our journey from high-growth scale-up to IPO and beyond. If you want to shape-not just support-how a leading tech company rewards its people, this is [. .. ] things equity. Vendor Compliance Management: You manage our equity platform provider, ensuring data integrity and seamless employee experience, while partnering with Legal, Tax, and Finance to maintain compliance across global regulatory requirements (409A, tax reporting) . Strategic Business Partnering: You collaborate with Talent, People, and Finance to diagnose talent challenges, design reward solutions, and model budget impacts-acting as a trusted advisor to leadership on compensation strategy and market positioning. Compensation Cycles Governance: You support annual performance and compensation review cycles, [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Finance Consultant (m/w/d)
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] compensation, benefits, health and safety, and employee support Support the development and optimization of efficient HR processes and administrative procedures Monitor compliance with internal policies as well [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as legal and regulatory requirements Identify, assess, and mitigate potential legal risks and support the prevention of liability and litigation issues Ensure compliance with legal requirements relating to the companys business premises and operational framework Being responsible for compliance with the requirements of ISO 27001 and supporting security awareness across the organization Contracts, Commercial [. .. ] degree or diploma in Accounting, Economics or equivalent Experience with the German rules and regulations for the area A mandatory requirement is that you master the German language, both in writing and orally. Besides, you master English at a level to be able to work internationally You are Berlinbased or have easy access to the city as we work in the office most of the week About us A common trait in c Brain is to be passionate about software, and we [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Berlin
[. .. ] and Industry Knowledge Comprehensive understanding of IT services markets Knowledge of AI application implementation challenges across different industries for Cloud Services Understanding of regional differences in AI [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] capabilities, adoption trends, regulatory requirements, etc for cloud models. Awareness of ethical, regulatory, and governance issues surrounding AI deployment Understanding of the impact of AI on enterprise cloud services procurement and decision-making processes Ability to translate Services technical capabilities into business value propositions Communication And Presentation Skills Exceptional writing abilities with experience creating research reports and thought leadership content Strong presentation skills and ability to communicate complex topics to non-technical audiences Experience conducting interviews with industry experts and C-level General Managers Ability to facilitate discussions and working sessions with diverse stakeholder groups Clear communication of data-driven [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Regulatory Affairs Manager posted about 2 months ago Belle Health AI Technologies Berlin, Germany
• Berlin
#
Regulatory Affairs Manager Posted on November 24, 2025 (4 months ago) # About Belle Health Belle Health is a women9s health company focused on developing digital medical devices [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to empower women to respond to their menstrual cycle-related challenges in an instant, safe, and drug-free way. Currently, we are [. .. ] drive process improvements. # About you Excellent written and oral communication skills in English. Interest in developing your career towards a PRRC role, if not qualified yet. Solid experience writing clean and compact technical documentation under MDR and ISO 13485. Bonus points for experience with software development, ISO 27001, GDPR, and knowledge of Di GAV in Germany, and German-speaking. 1. We are dedicated to female healthcare and aim to make a significant impact on the lives of menstruating individuals worldwide. [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Berlin
[. .. ] features that are truly patient-centric Responsibilities The Principal/ Senior Principal Clinical Outcome Assessment (COA) Endpoint Strategy serves as the senior scientific authority for COA endpoint strategy, endpoint [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development, COA regulatory strategy, and COA instrument science in client engagement and 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 advisor to pharmaceutical and biotechnology sponsors and represents IQVIA as an external scientific [. .. ] 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 5 Tagen bei Jobleads gefunden
Senior/ Staff Frontend Engineer (React) - Remote friendly
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] small things done right. Communication skills: you explain your thoughts in a clear, organized, concise and accurate manner. AI fluency good judgement: you can leverage AI to [...]
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[...] move faster (research, writing, coding, testing) while staying critical, validating outputs, and protecting the products reliability and user trust. At Qonto we understand that true diversity isnt just about ticking boxes on a hiring checklist. Apply regardless of the boxes you tick Who knows? You may have the missing piece of the puzzle weve [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Berlin
Jobticket
[. .. ] platform: simple digital access to capital markets through a single API. Our AP Ifirst infrastructure abstracts brokerage complexity with a welldocumented API, a selfservice customer operations portal, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and a clear regulatory framework, so partners can launch customercentric, compliant products in weeks, not months. Weve seen firsthand how expensive, slow, and complex brokerage infrastructure can be. We remove that friction for partners and their customers, making investing easier to offer, and easier to use. Your Mission: Your mission is to manage develop [. .. ] to help our partners expand their product offering and steer the process around it. Build out all processes design the framework standards for the Partner Management function. Embrace a strong writing culture help us deepen our understanding by sharing your knowledge partner insights proactively. You will be successful in this role if: Growing investing opportunities excites you. Our mission resonates with you, because you have worked in the financial sector before, ideally in a Brokerage Firm or a Fintech. You have [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
(Senior) Partner Manager (f/m/x)
• Berlin
Jobticket
[. .. ] makes launching an investment product customercentric and compliant. We abstract all complexity for our partners through a well documented API, a selfservice customer operations portal and operating [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a clear regulatory framework. Enabling partners to launch in weeks, not months. We have experienced first hand that brokerage infrastructure is broken. Building an investment product used to be highly expensive, challenging and cumbersome. We ease this pain by shielding our partners their customers from the underlying complexity and with that, we make [. .. ] to help our partners expand their product offering and steer the process around it. Build out all processes design the framework standards for the Partner Management function. Embrace a strong writing culture help us deepen our understanding by sharing your knowledge partner insights proactively. You will be successful in this role if: Growing investing opportunities excites you. Our mission resonates with you, because you have worked in the financial sector before, whether its a Brokerage Firm, a Bank or a Fintech. [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Giengen an der Brenz, Baden- Württemberg
[. .. ] You You add your ingredients to the planning, coordination, and execution of medical and scientific research projects, including clinical trials. You ensure the recipes for Good Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Practice (GCP) and regulatory requirements are followed. You assist in study documentation, data collection, and data management. You become a regular in coordinating communication between investigators, sponsors, CROs, and study teams, as well as in aligning 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 8 Tagen bei Jobleads gefunden
Senior Director, Analyst Data Analytics and AI Transformation in Procurement
• Berlin
Führungs-/ Leitungspositionen
[. .. ] and stakeholder engagement. Recognized as a thought leader in AI for procurement, with a portfolio of published research, industry presentations, or advisory engagements. Up-to-date knowledge of AI [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trends, regulatory considerations, and best practices in procurement transformation. Deep expertise in AI/ ML trends and experience applying those trends to redefine the future of procurement. What you will need Bachelors degree or equivalent experience; Graduate degree preferred 12+ years of relevant field or industry experience Demonstrate executive presence; can immediately establish credibility with executives and additional stakeholders Strong organizational skills; ability to work under tight deadlines and produce high quality deliverables Demonstrate excellence in research and writing ability Strong written and verbal proficiency, analytical and presentation skills; ability to engage clients and respond effectively to questions Proficient in analyzing and synthesizing data; can effectively apply patterns and frameworks while drawing and defending conclusions to client challenges Strong communicator who is able to explain complex concepts concisely and [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Berlin
[. .. ] CT) to support accurate and efficient diagnoses. Youll work handson with modern deep learning frameworks and take responsibility in missioncritical ML design choices to ensure that models [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meet clinical and regulatory standards. In this role, youll have the chance to drive the endtoend evolution of medical AItransforming complex research experiments into highimpact, productionready diagnostic tools that define the future of radiological care. Your Responsibilities Advance the development of highperformance computer vision architectures to detect and diagnose medical conditions within complex radiological [. .. ] ability to contribute to largescale codebases and handle complex datasets in a collaborative environment. Commitment to robust software engineering practices: including version control (Git) , unit testing, CI/ CD, and writing clean, maintainable code. What You Can Expect Focus on what matters: At our company, competence, personality, and commitment are more important than formalities or the study program you chose. Your Impact: Your work helps make disease diagnosis faster, more precise, and more manageable. Your Team: Join a highly motivated, interdisciplinary [. .. ]
Job am 24.03.2026 bei Jobleads gefunden
Regulatory Affairs Manager (m/f/x) Heidenheim/Berlin/ Porto/ Riga/ remote
• Berlin
General Information Position:
Regulatory Affairs Manager (m/f/x) Location: one of our offices in Heidenheim a. d. Brenz, Berlin, Porto, Riga, or remote (Germany/ Portugal/ Latvia) Starting: at the next [...]
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[...] possible date Your New Waters The FORCE builds companies for companies in the healthcare, pharmaceutical, and medical devices sector. We encourage work in [. .. ] 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 21.03.2026 bei Jobleads gefunden
(Associate) Officer Ethics and Conduct-based in Luxembourg
• Berlin
[. .. ] including strong exposure to areas related to legal drafting and/or corporate governance, and/or policy development, and/or other areas relevant to the remit of the Unit Knowledge of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory rules on corporate governance Knowledge of and/or experience in best practices regarding individual ethical conduct Knowledge and/or experience in issues related to OCCOs activities (e. g. Governance, regulatory standards and compliance, reporting to governing bodies, risk related files and KPIs, Whistleblowing, professional duties, Ethics) Knowledge of the EIB Groups objectives, mission broader policies Very good drafting abilities, in particular in relation to documentation/ files that have legal implications Good communication, presentation and writing skills Excellent knowledge of English and/or French () , with a good command of the other. Knowledge of other EU languages would be an advantage. Competencies About Find out more about EIB core behavioural skills here To find out more about our eligibility criteria click here () Unless stated [. .. ]
Job am 20.03.2026 bei Jobleads gefunden
Senior Product Manager-Accounting Domain
• Berlin
[. .. ] experts to ship features that make a real difference for SMEs and accountants. Go deep on accounting workflows: Youll develop a sharp understanding of how accounting actually [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] works-production workflows, regulatory constraints (einvoicing, FEC, OEC) , and the daytoday pain points of both SMEs and their accountants. Ship faster with AI: Youll use AI tools (Dust, Notion AI, Claude. . . ) and leverage AI as a product lever-identifying where automation and intelligence can transform accounting from a chore into [. .. ] you ship. You think in outcomes, not features, and youre comfortable making hard tradeoffs. AInative workflow: You use AI to supercharge how you work-from research and analysis to spec writing and user testing. You see AI as a product lever, not just a productivity hack. Track record of shipping: You have 5+ years of experience as a PM, with concrete examples of products you took from 0 to 1 or significantly scaled. Strong communication in English: You collaborate effectively across [. .. ]
Job am 19.03.2026 bei Jobleads gefunden
Regulatory Affairs Manager (m/f/x) - Heidenheim/Berlin/ Porto/ Riga or remote
• Berlin, Hamburg, Heidenheim an der Brenz, Baden- Württemberg
GENERAL INFORMATION We are looking for a
REGULATORY AFFAIRS MANAGER (m/f/x) Location: Heidenheim/Berlin/ Porto/ Riga or remote Starting: at the next possible date You dont always swim with the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] tide: In a growing company, we are looking for people who dont feel like a fish out of water in new situations and with new customers. [. .. ] 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 19.03.2026 bei Jobleads gefunden
CRO Product Owner (m/f/d)
• Berlin
[. .. ] systems (e. g. , Google Tag Manager, Matomo) Strong understanding of web analytics and user behavior metrics Analytical mindset with the ability to turn data into clear, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] testable ideas Comfortable writing technical specs or user stories for development teams Detail-oriented, conscientious, and confident in making decisions Excellent collaboration and communication skills Fluent in English; German is a plus About us We Love X is a leading force in the affiliate space, dedicated to ensuring that advertising always adds value. Starting [. .. ] set job alerts for Risk Compliance Officer roles. Senior EU Transport Compliance Manager, EU Fleet Compliance Team Sr Manager, EU EXR Programs, EU EXR Risk, Project Compliance Fund Compliance Manager (Regulatory Reporting) (m/f/d) Manager Financial Crime, Compliance und Conduct-Consulting (Financial Services) (w/m/d) (Senior) Product Compliance Manager (m/w/d) Compliance Systems Enablement Senior Manager Principal IT Operations Compliance Manager (d/f/m) Manager Kapitalmarkt-Compliance/ Crypto Assets Compliance-Consulting (Financial Services) (w/m/d) Manager IT-[. .. ]
Job am 17.03.2026 bei Jobleads gefunden
Medical Affairs Lead
• Berlin
Führungs-/ Leitungspositionen
[. .. ] posters, manuscripts, and conference presentations Coordinate publication planning and execution in partnership with the Medical Director and external collaborators Review all external-facing materials for clinical and scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accuracy Support regulatory documentation with clinical evidence summaries and scientific context KOL Engagement Clinician Education Build and maintain relationships with Key Opinion Leaders, academic partners, and clinical collaborators Develop and deliver training programs and educational materials for clinical users of Nucs AI products Organize and support advisory boards, clinical workshops, and scientific symposia [. .. ] 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 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Regulatory Writing pro Jahr?
Als Regulatory Writing verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Regulatory Writing Jobs in Berlin bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 77 offene Stellenanzeigen für Regulatory Writing Jobs in Berlin.
Wieviele Unternehmen suchen nach Bewerbern für Regulatory Writing Jobs in Berlin?
Aktuell suchen 30 Unternehmen nach Bewerbern für Regulatory Writing Jobs in Berlin.
Welche Unternehmen suchen nach Bewerbern für Regulatory Writing Stellenangebote in Berlin?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Regulatory Writing Stellenangebote in Berlin:
- Novanta (4 Jobs)
- Noah Labs (2 Jobs)
- IQVIA (2 Jobs)
- Sum Up (2 Jobs)
- JP Morgan Chase Co. (2 Jobs)
- Pharmtrace klinische Entwicklung GmbH (1 Job)
Zu welchem Berufsfeld gehören Regulatory Writing Jobs in Berlin?
Regulatory Writing Jobs in Berlin gehören zum Berufsfeld Technische Dokumentation / Redaktion.
