26 Jobs für Clinical Drug Specialist
Stellenangebote Clinical Drug Specialist Jobs
Job vor 13 Tagen bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or related field [...]
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[...] 1-3 years clinical research experience German language proficiency is essential for direct communication with the Competent Authority and Ethics Committees. Good interpersonal communication and organizational skills. Good technology skills and knowledge of MS Office applications. Good attention to detail. General awareness clinical trial environment and drug development process. Ability to work on multiple projects. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. IQVIA is a leading global provider of clinical research services, commercial insights and [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
IQVIA
Regulatory Start Up Specialist I, IQVIA Med Tech, Austria
• AT- 9 Wien
[. .. ] Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. Qualifications B Sc Degree in Life Sciences or related field [...]
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[...] 1-3 years clinical research experience German language proficiency is essential for direct communication with the Competent Authority and Ethics Committees. Good interpersonal communication and organizational skills. Good technology skills and knowledge of MS Office applications. Good attention to detail. General awareness clinical trial environment and drug development process. Ability to work on multiple projects. Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. Ability to work independently, to problem-solve collaboratively and to raise issues appropriately as needed. IQVIA is a leading global provider of clinical research services, commercial insights and [. .. ]
Job gestern bei Jobleads gefunden
• Hamburg
Führungs-/ Leitungspositionen Freiberuflich
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
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[...] resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior/ Medical Director (Neurology-Bid Defense Support) . About this role TFS Health Science is seeking a highly flexible board-certified Neurology specialist to support upcoming Bid Defense Meetings. This freelance role involves contributing expert input during proposal preparation (e. g. protocol review) and participating in the Bid Defense Meeting itself. Ideally, the successful candidate would also be available for medical monitoring support if the project is awarded although this is not a [. .. ] shaping study design, leading bid defenses and ensuring medical oversight across key projects. If you are a clinically grounded leader with a strong commercial mindset and a passion for advancing drug development, we invite you to join our global team. Key Responsibilities Strategic Leadership : Act as a key scientific advisor in bid defense meetings (BDM) , RFP responses, and proposal development, ensuring compelling and medically sound strategies. Study Design Protocol Development : Provide expert input on trial design, patient recruitment, [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Senior Tech Management Lead (m/f/x) Drug Product
• Pfaffenhofen an der Ilm, Bayern
Führungs-/ Leitungspositionen
Senior Tech Management Lead (m/f/x)
Drug Product Join to apply for the Senior Tech Management Lead (m/f/x) Drug Product role at Daiichi Sankyo Europe Gmb H Job Title: Senior Tech [...]
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[...] Management Lead (m/f/x) Drug Product Posting Start Date: 02/ 12/ 2025 Job Description For our development and production site in Pfaffenhofen/ Ilm we [. .. ] to internal and external sites Review technical documentation (protocols, reports) associated with manufacturing, tech transfer, sitetosite transfers and PPQ as needed Manage and conduct scouting activities and recommend CDMOs for clinical and launch site selection from Tech Mgmt. Drug Product perspective Create, communicate and implement technology transfer and manufacturing plans at the site which are aligned with crossfunctional CMC strategic discussions. Manage timelines, deliverables, and coordinate the input of technical and functional experts as needed Communicate outcome of key meetings to [. .. ] Fulltime Job function Project Management and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Daiichi Sankyo Europe Gmb H by 2x Get notified about new Technical Management Specialist jobs in Pfaffenhofen an der Ilm, Bavaria, Germany. #J-18808-Ljbffr 71850736 [. .. ]
Job gestern bei Jobleads gefunden
Head of Sales Marketing Department, PMLS Division, EU Location: Germany Responsibilities Provide product, marketing, and
clinical support to customers, as well as to sales and marketing managers, during inservices, presales [...]
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[...] activities, evaluations, followup visits, and troubleshooting efforts related to the PMLS product line. Collaborate with Product Managers and Engineering teams to enhance existing products and assist in the development of new ones, including identifying target markets [. .. ] veterinary specialty areas, with direct use of equipment such as endoscopy systems, veterinary telemetry systems, anesthesia machines, IV or syringe pumps, and monitoring devices. Solid understanding of ventilation modes, anesthetic drug delivery, and invasive blood pressure (IBP) monitoring. Prior experience in educating veterinary technicians or DVMs on medical equipment, ideally through structured staff development or preceptorship programs, is strongly preferred. Excellent verbal communication and presentation skills for conducting customer training. Strong interpersonal skills with the ability to engage effectively with various [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Clinical Account Specialist
• Berlin
Clinical Account
Specialist (CAS) The Clinical Account Specialist (CAS) position is a temporary role extending through mid-2027, but it presents an exciting opportunity to become part of our growing [...]
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[...] organization. If youre seeking to advance your sales career into a specialized field, this role could be an excellent next step. The CAS [. .. ] experience Ideally, experience in ophthalmology or a comparable scientifically focused indication area as well as in complex structures such as clinics and networks Profound understanding of the pharmaceutical industry and drug reimbursement in Germany Very good communication skills, integrity, convincing personality and confident appearance in a medical environment High willingness to travel Successful networker and team player Strong goal orientation, selfmotivation, the will to succeed and strong contacts with a pronounced customer orientation Good skills to develop innovative and creative solutions [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] for tardive dyskinesia, chorea associated with Huntingtons disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid-to [...]
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[...] late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, [. .. ] planning, and execution of the clinical development plan, including Phase 1 to 4 clinical studies in collaboration with cross-functional project team members, including clinical operations, clinical pharmacology, biometrics, regulatory, drug safety/ pharmacovigilance. The Executive Medical Director will also partner with medical affairs, HEOR, and commercial to provide guidance on publication strategy, data generation needs, and label expansion opportunities for marketed products. Your Contributions (include, but are not limited to) : Oversight of the clinical development strategy in the endocrinology therapeutic [. .. ] of data and identification of evidence generation needs Adhere to Neurocrine Europe quality assurance system and compliance with the relevant SOPs Requirements: The appointed candidate will be a physician with specialist experience/ qualifications in endocrinology and/or a proven track record of clinical development in endocrinology products. MD qualified, ideally with specialist medical qualification in Endocrinology and previous experience in patient care At least 8 years experience in early or late stage clinical development in the pharmaceutical industry, ideally including experience [. .. ]
Job am 01.11.2025 bei Jobleads gefunden
Medical Writer-Promotional Review
• Hannover, Niedersachsen
Senior Scientific Communications
Specialist English (Medical Writer/ Promo Review) Location: Fully Remote Europe Essentials Degree: Advanced degree in Pharmacy (Pharm D preferred) , advanced healthcare degree, or equivalent
clinical [...]
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[...] experience. Experience: 24 years in scientific content creation within the pharmaceutical industry, medical education, or academia. Languages: Fluent in English and German (C1/ C2) . Position Summary The Senior Scientific Communications Specialist provides scientific and medical writing support across multiple therapeutic areas. This role ensures the delivery of accurate, balanced, [. .. ] and organizational skills. Proficiency in Microsoft Office; familiarity with Embase, Ovid, and content management systems preferred. Solid understanding of pharmaceutical, regulatory, and compliance environments (FDA, EMA) . Demonstrated expertise in drug information communication and scientific content management. Team-oriented, adaptable, and able to manage multiple priorities in a fast-paced, client-driven setting. Displays professionalism, initiative, and leadership in cross-functional collaborations. Core Competencies Accuracy Time Management Communication Leadership Collaboration Innovation Customer Focus Work Ethic Self-Motivation Technical Aptitude Applied Learning [. .. ]
Job am 26.10.2025 bei Jobleads gefunden
• Kaarst, Nordrhein- Westfalen
Join to apply for the Field Customer Support
Specialist role at Charles River Laboratories 4 days ago Be among the first 25 applicants Join to apply for the Field [...]
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[...] Customer Support Specialist role at Charles River Laboratories Get AI-powered advice on this job and more exclusive features. For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, [. .. ] Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20, 000 employees within 110 facilities in over 20 [. .. ]
Job am 12.10.2025 bei Jobleads gefunden
Clinical Application Specialist Ultrasound (m/w/d) Region Nord
• Leipzig, Sachsen
Firmenwagen Jobticket
Clinical Application
Specialist Ultrasound (m/w/d) Region Nord page is loaded Clinical Application Specialist Ultrasound (m/w/d) Region Nord Apply locations Germany-Home Based time type Full time posted on Posted [...]
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[...] 2 Days Ago job requisition id 554984 Job Title Clinical Application Specialist Ultrasound (m/w/d) Region Nord Job Description [. .. ] require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/ Vets and maintains a drug-free workplace. #J-18808-Ljbffr 65792415 [. .. ]
Job am 12.10.2025 bei Jobleads gefunden
• Hamburg
Beratungs-/ Consultingtätigkeiten
Jobticket
Remote Service
Specialist (m/w/d) Monitoring page is loaded # # Remote Service Specialist (m/w/d) Monitoringlocations: Hamburgtime type: Full timeposted on: Posted Todayjob requisition id: 557850 # # # Job [...]
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[...] Title Remote Service Specialist (m/w/d) Monitoring # # # Job Description In dieser Position hast du die Möglichkeit [. .. ] technologies and innovations that improve peoples lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep Respiratory Care and Personal Health. Together, we deliver better care for more people because we believe that every human matters. Thats why were taking steps to create an environment where we acknowledge and embrace our [. .. ] require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/ Vets and maintains a drug-free workplace. #J-18808-Ljbffr 65792386 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Bauingenieur:in als Senior Projektleiter:in für Umbauten 80100
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Flexible Arbeitszeiten Work-Life-Balance
[. .. ] Lead, RLT Senior Project Manager IT and Digitalisation Technical Project Manager HVAC, Cleanroom, EMS, ALC Manager Global Business Excellence--Temporary position Muttenz, Basel-Country, Switzerland 1 year ago Global [...]
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[...] Drug Regulatory Affairs Project Leader (6602) Associate Director, Technical Project Leader Drug Substance Senior Project Manager: Public Infrastructure Finance for Municipal Development Permanent contract Analytical Project Leader Senior/ Principal Scientist Lead, Real World Sciences Application Strategy m/f/d Drug Product Project Leader Oral Dosage Forms (80-100) Consultant Technology Transfer-Fill Finish Team Lead MES PI Competence Center (f/m/d) , 80-100 Senior Global Business Process Specialist Financial Accounting Senior Clinical Operations Manager-6575 Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 65375776 [. .. ]
Job am 02.10.2025 bei Jobleads gefunden
• Schlieren, Zürich
At Biognosys, we believe that deep proteome insights hold the key to breakthrough discoveries that can dramatically improve human health. We enable life science researchers and
drug hunters to [...]
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[...] look at the proteome from every angle with our versatile portfolio of proprietary next-generation proteomics services, software, and kits, including the True Discovery, True Target, and True Signature platforms and flagship software Spectronaut. These solutions provide a multi-dimensional view of protein expression, function, and structure in [. .. ] to quantify thousands of proteins across thousands of samples with industry-leading precision, depth, and throughput. Through advanced data analytics, Biognosys translates data into actionable insights for R D and clinical research. Since January 2023, Biognosys is part of the Bruker family (Nasdaq: BRKR) aiming to make proteomics globally accessible. THE OPPORTUNITY Business Development Manager, UK Nordics, 100 We are seeking an experienced, enthusiastic, self-motivated, and people-oriented individual to join our rapidly growing EMEA commercial team. The role of [. .. ] us in a rapidly emerging and innovative market. DEPARTMENT: CRO Business Development and Commercial Support COMPANY: Biognosys AG LOCATION: Wagistrasse 21 8952 Schlieren Switzerland CONTACT: Arina Klein, (Senior Human Resources Specialist) Telephone: +41 44 244 50 18 #J-18808-Ljbffr 64141450 [. .. ]
Job am 20.09.2025 bei Jobleads gefunden
Clotrimazole and Betamethasone Lotion: A Comprehensive Overview
• München, Bayern
Clotrimazole and also betamethasone cream is a mix
drug that is commonly made use of for the therapy of different skin conditions. This unique formula integrates the antifungal medicine [...]
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[...] clotrimazole with the corticosteroid betamethasone, supplying a twin activity for effective remedy for itching, inflammation, as well as infections. In this write-up, we will check out the usages, advantages, [. .. ] skin shade If you experience extreme skin irritation, signs of an allergic reaction, or any other concerning negative effects, stop use of the lotion as well as look for immediate clinical interest. Conclusion: Clotrimazole and also betamethasone cream is a powerful mix medicine utilized for the therapy of numerous skin conditions. Combining the antifungal homes of clotrimazole with the anti-inflammatory impacts of betamethasone, this cream provides relief from itching, inflammation, and fungal infections. It is important to utilize this lotion as routed by a health care specialist as well as to be familiar with prospective negative effects. Speak with a health care specialist for customized suggestions and support regarding making use of clotrimazole as well as betamethasone hanker your specific problem. #J-18808-Ljbffr 62673050 [. .. ]
Job am 19.09.2025 bei Jobleads gefunden
Abgeschlossene Ausbildung
Firmenwagen Jobticket
# # # Job Title
Clinical Application
Specialist Ultrasound Region Bayern (m/w/d) # # # Job Description Verantwortlich für den klinischen Support von Kunden vor und nach dem [...]
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[...] Verkauf im Ultraschall Business für den Süden von Deutschland, v. a. für das Gebiet Bayern. Dein Job: Medizintechnische Geräte in ihrem jeweiligen Einsatzumfeld (Kliniken, Praxen, OPs, usw. [. .. ] require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/ Vets and maintains a drug-free workplace. #J-18808-Ljbffr 62545330 [. .. ]
Job am 01.07.2025 bei Jobleads gefunden
Clinical Trial Site Relationship Coordinator
• München, Bayern
Clinical Trial Site Relationship Coordinator Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations [...]
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[...] team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain [. .. ] of Science in health-related field; Minimum 1 years site and clinical trials experience (more experience for the more senior positions required) ; CRA experience is an asset; Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred; Knowledge of medical terminology and clinical patient management preferred; Fluency in English; German; Demonstrated organizational and prioritization skills; Excellent oral and written communication skills; and Proficient knowledge of Microsoft Office applications. We kindly ask to send applications in English. [. .. ] type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Medpace by 2x Clinical Trial Associate/ Specialist (CTA/ CTS) Freelance Clinical Trials Site Coordinator Sponsor Dedicated Clinical Trial Assistant in Munich area Senior Clinical Research Associates (experienced) - Germany (Senior) Research Manager-Spine Neurosurgery Expert Clinical Trials Statistics and Programming Working Student-Clinical Data Processing (m/f/d) Were unlocking community knowledge in a new way. Experts [. .. ]
Job am 18.06.2025 bei Jobleads gefunden
• München, Bayern
Imiquimod cream is a to tonerin capsule prezzo pical
drug that has actually acquired substantial attention in the field of dermatology. It is typically utilized to deal with various [...]
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[...] skin disease, providing relief as well as enhancement for patients. This short article intends to discover the usages, advantages, and possible side effects of imiquimod cream. Imiquimod cream belongs to a [. .. ] favor non-invasive alternatives. Imiquimod lotion is commonly used in a slim layer to the affected area 5 times a week for several weeks, under the guidance of a healthcare specialist. Routine follow-up gos to are necessary to check the progression of basic cell cancer sores as well as ensure the effectiveness of the therapy. In many cases, a combination of imiquimod lotion and various other therapy methods, such as cryotherapy or surgical treatment, might be advised to attain optimum [. .. ] adverse effects might happen, such as blistering, ulcer, or modifications in skin coloring. If any type of unusual or consistent adverse effects are experienced, it is very important to seek clinical interest promptly. Imiquimod lotion is a valuable drug for the therapy of different skin problem, offering both healing as well as cosmetic advantages. Whether used for actinic keratosis, genital blemishes, or basic cell cancer, imiquimod cream has actually revealed effectiveness in addressing these problems. Nevertheless, it is essential to speak [. .. ]
Job gestern bei Neuvoo gefunden
Parexel
Clinical Trial Specialist/ Senior Clinical Trial Associate
• Berlin
When our values align, theres no limit to what we can achieve. Parexel is beginning to search for an experienced Senior
Clinical Trial Administrator to join one of our [...]
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[...] key sponsors in the Clinical Trial Specialist. In this role you will provide technical and administrative support to the clinical study teams responsible for clinical trial execution. Some specifics about this advertised role Support moderately complex clinical study activities in support of the Clinical Trial Manager. Work closely with the clinical trial team to ensure trial activities [. .. ] areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of todays top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. Youll be an influential member of the wider team. What we are looking for in this role For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
Charles River Laboratories, Inc.
• Erkrath, North Rhine- Westphalia
Work-Life-Balance
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new
drug therapies. When you join our family, you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. Job Summary As a Sales Support Specialist, you will be responsible for achieving quarterly and annual sales targets for Biologics Testing services in your assigned territory. The role involves engaging with prospects and existing customers while guiding customers to Biologics services that best meet their needs. Note: Its a fully remote role with some business travel requirements. [. .. ] characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20, 000 biologic testing reports are sent each and over 200 licenses products are supported by [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
Charles River
Biologics Testing-Sales Support Specialist-(m/f/d)
• Erkrath, North Rhine- Westphalia
Work-Life-Balance
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new
drug therapies. When you join our family, you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. Job Summary As a Sales Support Specialist, you will be responsible for achieving quarterly and annual sales targets for Biologics Testing services in your assigned territory. The role involves engaging with prospects and existing customers while guiding customers to Biologics services that best meet their needs. Note: Its a fully remote role with some business travel requirements. [. .. ] characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20, 000 biologic testing reports are sent each and over 200 licenses products are supported by [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
Siegfried
Personalleitung (m/w/d)
• Hamelin, Lower Saxony
[. .. ] stage Research Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R D [...]
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[...] material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products. What we do in Hameln Hameln is a renowned contract manufacturer which supplies both national and international pharmaceutical companies. It has over 450 employees who produce sterile medicinal products, mainly for use in hospitals and intensive care facilities. Main activities Contract manufacture of parenteral solutions and suspensions aseptic or terminally sterilized in ampoules and vials Specialist in the production of complex preparations such as anesthetics, flammable and oxygen-sensitive liquids and cold chain products Special features Successful transfers and establishment of new products in sterile production Batch size: up to 3500 liters Clean room area: 4000 m Batch manufacture and filling of sterile products, from visual [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
Pro Pharma Group
Multilingual Medical Information Specialist-German Speaking
• Berlin
[. .. ] 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 [...]
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[...] sciences, clinical research solutions, quality compliance, pharmacovigilance, medical information, and R D technology, Pro Pharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Were looking for a Multilingual Medical Information Specialist to join our Medical Information Department. You will be responsible for providing a high-quality Medical Information service via phone and email following full training on designated clients/ products. Were looking for candidates who can speak and write at C1 level in both German and English and we will offer [. .. ]
Job vor 12 Tagen bei Neuvoo.com gefunden
S3 Science Recruitment
Regulatory affairs CMC Specialist
• Munich
Regulatory Affairs
Specialist CMC Location: Germany (Hybrid/On-Site) Employment Type: Permanent Overview We are seeking an experienced Regulatory Affairs Specialist with strong CMC expertise to join our growing team. This [...]
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[...] role is ideal for someone with a rigorous scientific background (Masters or Ph D required) and hands-on experience supporting regulatory submissions across [. .. ] and late-stage development. Key Responsibilities Prepare, review and maintain CMC documentation for global regulatory submissions (IND, IMPD, CTA, MAA, NDA, BLA) . Support regulatory strategy for CMC topics across drug substance and drug product. Contribute to scientific advice meetings, briefing books, and responses to health authority queries. Ensure alignment of CMC development activities with applicable guidelines (EMA, FDA, ICH) . Collaborate closely with Quality, Process Development, Analytical, and Clinical teams to ensure regulatory compliance. Maintain oversight of CMC change controls and post-approval variations. Requirements Masters or Ph D in Life Sciences, Pharmacy, Chemistry, Biochemistry or related field (mandatory) . 37+ years of experience in Regulatory Affairs with a CMC focus. Demonstrated experience authoring, reviewing, or contributing to CMC modules [. .. ]
Job vor 12 Tagen bei Neuvoo.com gefunden
S3 Science Recruitment
Regulatory affairs CMC Specialist
Regulatory Affairs
Specialist CMC Location: Germany (Hybrid/On-Site) Employment Type: Permanent Overview We are seeking an experienced Regulatory Affairs Specialist with strong CMC expertise to join our growing team. This [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role is ideal for someone with a rigorous scientific background (Masters or Ph D required) and hands-on experience supporting regulatory submissions across [. .. ] and late-stage development. Key Responsibilities Prepare, review and maintain CMC documentation for global regulatory submissions (IND, IMPD, CTA, MAA, NDA, BLA) . Support regulatory strategy for CMC topics across drug substance and drug product. Contribute to scientific advice meetings, briefing books, and responses to health authority queries. Ensure alignment of CMC development activities with applicable guidelines (EMA, FDA, ICH) . Collaborate closely with Quality, Process Development, Analytical, and Clinical teams to ensure regulatory compliance. Maintain oversight of CMC change controls and post-approval variations. Requirements Masters or Ph D in Life Sciences, Pharmacy, Chemistry, Biochemistry or related field (mandatory) . 37+ years of experience in Regulatory Affairs with a CMC focus. Demonstrated experience authoring, reviewing, or contributing to CMC modules [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Medpace
Study Start-up Specialist
• Munich
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
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[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] 000 people across 40+ countries. Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator/ Study Start-up Specialist to join our Clinical Operations team in Munich. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. [. .. ] documents; Advise on changing country regulations and compliance requirements; and Track submissions and ensure timely filing of documents. Qualifications Bachelors degree (preferably in a Life Sciences field) ; Interest in drug development and clinical trials; Full professional proficiency in German and English in written and verbal communication; Knowledge of Microsoft Office; and Excellent organization and communication skills, great attention to detail. Travel: None We kindly ask to submit applications in English. We would appreciate if you could indicate the status of [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Specialist pro Jahr?
Als Clinical Drug Specialist verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 26 offene Stellenanzeigen für Clinical Drug Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Specialist Jobs?
Aktuell suchen 11 Unternehmen nach Bewerbern für Clinical Drug Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Drug Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Drug Specialist Stellenangebote:
- S3 Science Recruitment (2 Jobs)
- IQVIA Argentina (1 Job)
- IQVIA (1 Job)
- Parexel (1 Job)
- Charles River (1 Job)
In welchen Bundesländern werden die meisten Clinical Drug Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Specialist Jobs werden derzeit in Bayern (5 Jobs), Nordrhein-Westfalen (3 Jobs) und Berlin (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Specialist Jobs?
Clinical Drug Specialist Jobs gehören zum Berufsfeld Pharmazie.
