17 Jobs für Clinical Drug Consultant
Stellenangebote Clinical Drug Consultant Jobs
Job am 08.10.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] präsentierst wissenschaftliche Daten, Studienergebnisse und medizinisches Hintergrundwissen. Du entwickelst Kommunikationsformate für den Austausch mit KOL und nimmst an relevanten nationalen und internationalen Kongressen teil. Du bist die [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Schnittstelle zwischen Fachabteilungen Clinical Trials, Produktmanagement und Außendienst und schulst wissenschaftliche Inhalte nach innen und außen. Du hast ein erfolgreich abgeschlossenes medizinisches oder naturwissenschaftliches Studium. Du hast bereits 3 Jahre Berufserfahrung im Bereich Medical Affairs oder in vergleichbaren Themenfeldern gesammelt. Du zeichnest Dich durch eine selbstständige und strukturierte Arbeitsweise aus, regelmäßige berufliche Reisen siehst [. .. ] Menschen ein neues Leben Aus Gründen der besseren Lesbarkeit wird in dieser Anzeige die männliche Form verwendet. Sie bezieht sich ausdrücklich auf alle Geschlechter (w/m/d) . IT (Senior) Consultant für Regulatory Affairs, Medical Affairs oder Drug Safety-Life Science (w m d) Medical Science Liaison Hämatologie (all genders) für die Region Bayern Medical Science Liaison Hematology (München/ Nürnberg) (Sr) Medical Science Liaison Rare Diseases/ Friedreich Ataxie (FA) (f/m/d) Medical Science Liaison (m/w/d) Onkologie-Gastrointestinale Tumore (Norddeutschland) #J-18808-Ljbffr 65086292 [. .. ]
Job am 03.07.2025 bei Jobleads gefunden
• Kassel, Hessen
Führungs-/ Leitungspositionen
Discovery Life Sciences is a global market leader in biospecimen solutions and laboratory services, offering an extensive range of products and services to support
drug discovery and development. With a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] network of laboratories and offices across the United States and internationally, we are committed to advancing scientific research and improving health care outcomes. We are dedicated to accelerating the discovery and development of new therapies and diagnostics by providing the highest quality biospecimens, in vitro [. .. ] teams in assay development and validation which includes semiquantitative as well as quantitative assays Support/ consult our project management and business development team as well as our clients Evaluation of clinical trial specimens Act as a trainer for external pathologists within our post approval services for the interpretation/ scoring of novel biomarkers Preparation of publications/ posters in collaboration with our customers Position Qualifications (Education, Skills, Experience) : Board certification (German board certification preferred) Additional training in Cytology Experience in hematopathology and/[. .. ] on oncology and immunology Excellent knowledge in IHC, m IF, FISH, RNA in situ hybridization to support the assay development team as well as to act as an experienced reader and consultant for customers in clinical trials. Experience in digital imaging applications and the evaluation of biomarkers via digital image analysis software Teamplayer Willingness to work in a GCLP environment Compensation and Benefits: Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Zürich Zuerich
Homeoffice möglich
For our customer located in Zurich/ Switzerland we are currently looking for a : Manager Regulatory Affairs (remote) (m/f/x) Remote:
Consultant needs to be based in Switzerland, but the HM [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is flexible when it comes to home office, there might be just a few days needed onsite. Travel: Requires approximately 10 travel Tasks Responsibilities Objectives: Responsible for supporting the regulatory activities related to the development, registration and life cycle management of [. .. ] and life cycle management for vaccine candidates in the region Ensures that all necessary applications are filed and maintained in compliance with applicable regulations. Responsible for regulatory oversight of assigned clinical trials conducted in the region. Provides regulatory oversight for assigned projects, focused on non-clinical and clinical aspects of drug development/ approval and associated regulations. Collaborates with all regulatory counterparts to ensure alignment and execution of the global regulatory strategy for the assigned projects. Passion for quality in all areas of responsibility Leads and directs the work of others as part of a matrixed organization. Accountabilities: Close collaboration with the [. .. ]
Job gestern bei Jobleads gefunden
Führungs-/ Leitungspositionen
Overview Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional
drug discovery and development. Its clients include more than 2, 000 biopharmaceutical companies, academic institutions and [...]
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[...] regulatory agencies across 62 countries. At Certara, we accelerate medicines to patients by partnering with life science innovators. In the past 6 years, over 90 of companies that received new drug approvals by the FDA [. .. ] end platform with biosimulation, regulatory science, and market access solutions combined with our strong team of scientists and subject matter experts enable our clients to have informed decision-making, reduced clinical trial burden, higher R D productivity, improved patient outcomes and increased patient access to medicines, and accelerated regulatory approval. Informed decision-making reduced clinical trial burden Higher R D productivity Improved patient outcomes increased patient access to medicines Accelerated regulatory approval Certara is a global team that nurtures a diverse [. .. ] Responsibilities Support projects for Certaras clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands-on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Senior Principal
Consultant (Medical) at Bio Talent, part of The IN Group Bio Talent are delighted to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently [...]
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[...] hiring for a Global Head of Pharmacovigilance. This is a strategic leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. The role will direct safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. It is central to ensuring safe, compliant, and successful oncology drug development and maximising patient safety from clinical trials to postmarketing surveillance. This position will report to the Chief Medical Officer and may work on a hybrid basis from the company office in Germany or remotely. [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Frankfurt (Oder) , Brandenburg
Führungs-/ Leitungspositionen
[. .. ] clients and other internal departments, and applying advanced statistical methods to project work. Serve as a resource for the department, ensuring scientific integrity in the application of [...]
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[...] statistical methodology to clinical trials. Assist the Director in strategic planning and resource allocation for the department. Participate as senior statistician on major projects, including developing/ reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports. Assist the Director in proposal development, project allocations, budget projections, and [. .. ] more at Essential Functions Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Oversees team with same expectations. Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company. Maintains knowledge and awareness of developments in Biostatistics and clinical trial methodology, and regulatory requirements that impact analyses. Represent clients at meetings with regulatory agencies or other regulatory meetings, may participate as a member [. .. ] participate as high level lead biostatistician on major project (s) including developing/ reviewing protocols, preparing analysis plans, and writing sections of joint clinical/ statistical reports, integrated summaries and/or New Drug Applications (NDA) sections, as required. May be leading studies at an operational level until SAP writing begins. Management: Drive operational pieces of the business segment (e. g. resource management for a business segment, recruitment management for a business segment) . Provide expert review of process and initiate methodology development work [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
[. .. ] professionally. We recognize and value the importance of all people, the way we work, our drive for innovation and, most importantly, our patients. We are looking for [...]
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[...] a Senior Analyst Clinical Site Contracts, German Polish speaker to work 100 remotely in EU. The job is dedicated to one sponsor. This role will be part of the Site Contracts Budgets team, working to execute the clinical site contracts and budgets process for sponsor clinical development programs, from contract initiation to completion, maintenance, [. .. ] of work. Expect exciting professional challenges in inspiring studies, but with time for your outside life. Responsibilities Negotiate and maintain Clinical Trials Agreements (CTA) , site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable contracts. As required, oversee CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols. Ensures compliance of contracts with Fair Market Value (FMV) principles and guidelines. Track contract progress, complete [. .. ] and regulatory compliance issues. Strong interest in learning more about contracts and budgeting in support of Sponsor clinical trials. Working knowledge of clinical trial functions, including clinical operations, regulatory and drug safety. Ability to prioritize and manage multiple tasks simultaneously. Become part of a global community where you can turn your career into a lifetime achievement. #J-18808-Ljbffr 70499801 [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Kassel, Hessen
Senior Recruitment
Consultant Meet Marketing Masters Degree Location: Kassel, Germany (Hybrid) A leading global organisation in biospecimen solutions and advanced laboratory services is seeking an experienced Senior/ Director-level Pathologist [...]
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[...] to oversee its international pathology function and serve as Medical Director for its German site. The company partners with top pharmaceutical and biotech organisations to accelerate drug discovery, development, and diagnostic innovation. Key Responsibilities Lead, mentor, and develop an international team of pathologists. Maintain and expand a global pathology network. Provide medical leadership for the organisations site in Kassel, Germany. Optimise pathology-related processes and workflows. Guide and support assay development and validation (semi-quantitative quantitative) . Offer scientific consultation to internal teams and external clients. Evaluate clinical trial specimens to support research and development activities. Train external pathologists in biomarker interpretation/ scoring as part of postapproval services. Contribute to scientific publications and conference materials in collaboration with partners. What This Role Offers A strategic leadership position with significant scientific impact. Opportunity to shape pathology strategy across a [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Sr. Principal
Consultant, Regulatory Strategy and Advisory Sr. Principal Consultant, Regulatory Strategy and Advisory 1 month ago Be among the first 25 applicants All candidates should have a passion [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for helping our clients navigate transformational change; We are looking for smart, self-driven, high-energy people with top-notch communication skills, intellectual curiosity. [. .. ] and agile delivery experienced Role Summary, Core Expectations In depth knowledge of Pharma Regulatory Operations and Regulatory IT Systems aligned to core Functional and Technical competencies Expert in Regulatory and Clinical area with ability to drive futuristic IT solutions and experience in client facing and agency thought leadership Understanding and knowledge of processes related to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific regulatory requirements-keenly aware of industry trends, needs and business requirements [. .. ] outcomes Technical Credentials: Should have masters degree in a Life Science, Medical or Related discipline. Masters in Business Administration would be an added advantage. Minimum 12-15 years experience in Drug development, Regulatory, Clinical Operation and Medical Devices. Deep understanding of RIM systems i. e. , Veeva Vault, PARAXEL/ LIQUENT In Sight, CSC Regulatory Tracker, Aris Global Register, Open Text, Share Point, Documentum, First Doc/ First Point, Next Docs, CARA, Extedo e CTD Manager, Trackwise, or other regulatory information management systems Submission [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• 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 09.10.2025 bei Jobleads gefunden
Associate Business Consultant-Life Sciences R D and Quality
• Berlin
Beratungs-/ Consultingtätigkeiten
Overview Associate Business
Consultant-Life Sciences R D and Quality Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. [...]
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[...] As one of the fastest-growing Saa S companies in history, we surpassed 2B in revenue in our last fiscal year with extensive growth [. .. ] data, and consulting. We deliver unique value to this industry through excellent business consulting services powered by Veevas industry-leading software and data. Our R D and Quality teams accelerate drug development across the entire R D value chain-Clinical, Regulatory, Safety, and Quality. We optimize and unify digital operations for our customers to deliver therapies more efficiently, while ensuring patient safety. Learn more about our teams impact and thought leadership through our Resource Hub (see R D Strategy) . We hire Associate Business Consultants across our different teams. If [. .. ]
Job am 11.09.2025 bei Jobleads gefunden
Associate Business Consultant-Life Sciences R D and Quality
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
Associate Business
Consultant-Life Sciences R D and Quality Join to apply for the Associate Business Consultant-Life Sciences R D and Quality role at Veeva Systems. Overview Veeva Systems is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the [. .. ] on customer-facing engagements to create high-impact business solutions. We deliver value to the Life Sciences industry through software, data, and consulting. Our R D and Quality teams accelerate drug development across the entire R D value chain Clinical, Regulatory, Safety, and Quality. We optimize digital operations for our customers to deliver therapies more efficiently while ensuring patient safety. Learn more about our teams impact through our Resource Hub (see R D Strategy) . We hire Associate Business Consultants across our different teams. If multiple teams interest you, apply [. .. ]
Job am 31.08.2025 bei Jobleads gefunden
VP Pathology (m/f/d)
• Kassel, Hessen
Discovery Life Sciences is a global market leader in biospecimen solutions and laboratory services, offering an extensive range of products and services to support
drug discovery and development. With [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a network of laboratories and offices across the United States and internationally, we are committed to advancing scientific research and improving health care outcomes. We are dedicated to accelerating the discovery and development of new therapies and diagnostics by providing the highest quality biospecimens, in vitro [. .. ] teams in assay development and validation which includes semiquantitative as well as quantitative assays Support/ consult our project management and business development team as well as our clients Evaluation of clinical trial specimens Act as a trainer for external pathologists within our post approval services for the interpretation/ scoring of novel biomarkers Preparation of publications/ posters in collaboration with our customers Position Qualifications (Education, Skills, Experience) : Board certification (German board certification preferred) Additional training in Cytology Experience in hematopathology and/[. .. ] on oncology and immunology Excellent knowledge in IHC, m IF, FISH, RNA in situ hybridization to support the assay development team as well as to act as an experienced reader and consultant for customers in clinical trials. Experience in digital imaging applications and the evaluation of biomarkers via digital image analysis software Teamplayer Willingness to work in a GCLP environment Compensation and Benefits: Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total [. .. ]
Job am 27.08.2025 bei Jobleads gefunden
Director, Pharmacometrics
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] and the people that need them most. Innovation and creativity are highly valued, and everyone is given the opportunity for training and continuous development. Our portfolio spans [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the discovery, preclinical, clinical and post-marketing phases of drug development, working with 1, 200 commercial companies, 250 academic institutions, and numerous regulatory agencies. In the past 6 years, over 90 of companies that received new drug approvals by the FDA used our software or services. Our integrated and proprietary end-to-end platform with biosimulation, regulatory science, and market [. .. ] interests. Support projects for Certaras clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in [. .. ]
Job am 08.11.2025 bei Neuvoo.com gefunden
S3 Science Recruitment
CMC-Senior product developer
CMC
Consultant Looking for consultants ranging from a minimum if 5 years to 15+ years experience in CMC. The CMC Consultant acts as a subject matter expert across
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>drug substance and drug product development, covering a broad range of modalities (small molecules, oligonucleotides, biologics) and dosage forms (oral, sterile, nanoparticle formulations) . This role supports projects from pre-
clinical development through to commercial approval, ensuring CMC strategy, documentation and execution align with global regulatory expectations. Tasks Responsibilities Provide expert guidance on quality and CMC regulatory aspects of drug development, collaborating closely with cross-functional stakeholders. Ensure CMC work-packages and documentation are phase-appropriate, regulatory compliant and supportive of [. .. ]
▶ Zur Stellenanzeige
Job am 08.11.2025 bei Neuvoo.com gefunden
S3 Science Recruitment
CMC-Senior product developer
• Munich
CMC
Consultant Looking for consultants ranging from a minimum if 5 years to 15+ years experience in CMC. The CMC Consultant acts as a subject matter expert across
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>drug substance and drug product development, covering a broad range of modalities (small molecules, oligonucleotides, biologics) and dosage forms (oral, sterile, nanoparticle formulations) . This role supports projects from pre-
clinical development through to commercial approval, ensuring CMC strategy, documentation and execution align with global regulatory expectations. Tasks Responsibilities Provide expert guidance on quality and CMC regulatory aspects of drug development, collaborating closely with cross-functional stakeholders. Ensure CMC work-packages and documentation are phase-appropriate, regulatory compliant and supportive of [. .. ]
▶ Zur Stellenanzeige
Job am 20.10.2025 bei Job-Consult gefunden
PhD- Jobs. NET
Specialist Adult Psychiatry
• Schweden/ sonstiges/ Europa
[. .. ] supervision of younger colleagues is included as a natural part of the work and participation in the units medical development specialists perform the most physician specific tasks [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] such as diagnostics drug treatment and the establishment of a care treatment plan together with the team on the other hand psychotherapies are conducted by psychotherapists with other basic professionals dutywork is included in the service both daily and evening night duties you also need knowledge to replace your staff when vacation illness etc [. .. ] participating in the development of this we also wish you to have an interest in adhd treatment and substitution treatment for opiate addiction number of vacancies education specialist education psychiatry clinical experience what kind of treatments patients do you expect the doctor to have experience with years of experience all of the vacancies involve working with most of the psychiatric diagnoses why a broad background is a plus special knowledge and skills or special interests that are important to the job [. .. ] as a specialist your role will be to back up the residents when you get a delegation to deal with emergency care issues which usually happens when you get a consultant employment your duty will instead be a backup doctor to apply please send your cv mentioning reference lr at info phd jobs net contact person vitaly pryadka tel web http www phd jobs net gesundheits sozialwesen sonstiges europa medizin pharma sozialwesen vollzeit 66556414 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Consultant pro Jahr?
Als Clinical Drug Consultant verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 17 offene Stellenanzeigen für Clinical Drug Consultant Jobs.
In welchen Bundesländern werden die meisten Clinical Drug Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Consultant Jobs werden derzeit in Sachsen-Anhalt (3 Jobs), Hessen (3 Jobs) und Bayern (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Consultant Jobs?
Clinical Drug Consultant Jobs gehören zum Berufsfeld Pharmazie.
