14 Jobs für Clinical Drug Consultant
Stellenangebote Clinical Drug Consultant Jobs
Job am 14.01.2026 bei Jooble gefunden
Adragos Pharma GmbH
• München
Führungs-/ Leitungspositionen
[. .. ] for execution. You will coordinate across countries, manage cross-functional project teams, and be a key architect of the groups operating model. We are seeking a former top [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] tier strategy consultant or operational transformation leader with solid experience in pharmaceutical manufacturing or CDMO environments. You must have worked on complex post-merger integrations or site transformations. You combine analytical strength with a pragmatic, entrepreneurial approach. If you want to help shape the future of a global CDMO and work at the [. .. ] Contact HR-Team Adragos Pharma About us Adragos Pharma is a reliable Contract Development and Manufacturing Organization (CDMO) headquartered in Munich, Germany. We provide comprehensive development and manufacturing services for drug products, including sterile and non-sterile liquids, solids, and semi-solids. Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply. With production sites in Germany, France, Greece, Norway, Japan, and Switzerland, we ensure high-quality manufacturing across all stages of the drug development process. Founded in 2020, Adragos Pharma has rapidly grown through [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Infosys Consulting- Europe
• München
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 21.01.2026 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 [. .. ]
Job am 18.01.2026 bei Jobleads gefunden
• Au in der Hallertau, Bayern
Overview CRVCID 714205 Fiona Stanley Fremantle Hospitals Group (FSFHG) are seeking
Clinical Neuropsychologist Registrars and Clinical Neuropsychologists to join our Department of Clinical Psychology and Clinical Neuropsychology. This is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] recruitment pool for Permanent Full-Time/ Part-Time, Fixed-Term Full-Time/ Part-Time appointments, with the possibility of extensions (s) and/or permanency. We currently have multiple positions with immediate vacancies at Fiona Stanley Hospital and Cockburn Health Service. We encourage you to contact Hyranthi Kavanagh, Consultant Clinical Psychologist/ Head of Department on 08 6152 3477 or to discuss the pool vacancies. Position Profile We are seeking experienced, compassionate, and patient-centred Clinical Neuropsychologists with knowledge and experience in delivering neuropsychological assessments, reports and treatment recommendations to patients with complex medical, psychological, rehabilitation and mental health needs, [. .. ] and medical services. Fiona Stanley Hospital Cockburn Mental Health Facility is a 75-bed voluntary inpatient facility in Cockburn for womens mental health disorders, eating disorders and alcohol and other drug detoxification and recovery support. Our vision is excellent health care, every time. You can read more about SMHS in our Strategic Plan here. Values and Diversity Our Values guide our work in every action, and that includes recruitment and employment. SMHS encourages Aboriginal people, people from culturally and linguistically diverse [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Clinical Neuropsychologist Registrar/ Clinical Neuropsychologist
• Bayern
CRVCID 714205 Fiona Stanley Fremantle Hospitals Group (FSFHG) are seeking
Clinical Neuropsychologist Registrars and Clinical Neuropsychologists to join our Department of Clinical Psychology and Clinical Neuropsychology. This is a recruitment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pool for Permanent Full-Time/ Part-Time, Fixed-Term Full-Time/ Part-Time appointments, with the possibility of extensions (s) and/or permanency. We currently have multiple positions with immediate vacancies at Fiona Stanley Hospital and Cockburn Health Service. We encourage you to contact Hyranthi Kavanagh, Consultant Clinical Psychologist/ Head of Department on 08 6152 3477 or to discuss the pool vacancies. Position Profile We are seeking experienced, compassionate, and patientcentred Clinical Neuropsychologists with knowledge and experience in delivering neuropsychological assessments, reports and treatment recommendations to patients with complex medical, psychological, rehabilitation and mental health needs, to [. .. ] Fiona Stanley Hospital Cockburn Mental Health Facility is a 75bed voluntary inpatient facility inpatient mental health facility in Cockburn for womens mental health disorders, eating disorders and alcohol and other drug detoxification and recovery support. Our vision is excellent health care, every time. You can read more about SMHS in our Strategic Plan here. Our Values guide our work in every action, and that includes recruitment and employment SMHS encourages Aboriginal people, people from culturally and linguistically diverse backgrounds or LGBTI [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
Sabbaticals
[. .. ] will work cross-functionally and globally to embed sustainable access approaches across the product lifecycle. You will shape national HTA submissions, develop evidence-driven payer value propositions, and translate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complex clinical and economic data into strategic outcomes. This role will also offer exciting proximity to Modernas digital ambitions, with opportunities to work closely with real-world data and explore synergies with generative AI tools in evidence generation and access storytelling. Heres What Youll Do Your key responsibilities will be: Lead the [. .. ] real-world datasets into compelling payer value stories and clear evidence frameworks. Coordinate cross-functional teams (Market Access, HEOR, Medical, Commercial, external experts) for strategy execution. Act as an internal consultant to align local market insights with global product and platform plans. The key Moderna Mindsets youll need to succeed in the role: We digitize everywhere possible using the power of code to maximize our impact on patients. In this role, the ability to interface with large datasets, claims-based systems, [. .. ] join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work #J-18808-Ljbffr 72357105 [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
Sr. Principal Consultant, Regulatory Strategy and Advisory
• 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
• 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 27.08.2025 bei Jobleads gefunden
• 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 [. .. ]
Neu Job vor 6 Std. bei Neuvoo gefunden
IQVIA
Patient Site Engagement Opeations Specialist-Sponsor Dedicated (m/w/d)
• Frankfurt, Hessen
[. .. ] Functions Work together with strategy team to translate recruitment and retention strategy into operational and tactical plans to positively impact recruitment and retention rates for assigned projects [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Serve as internal consultant to project teams to implement operational recruitment plans on new and/or existing projects needing recruitment and retention services Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects (based on scope, may co-manage or independently manage these projects) Serve as primary operational project [. .. ] Bachelors Degree Health care or other scientific discipline or educational equivalent Req 6 yrs. of relevant industry experience. Equivalent combination of education, training and experience. In depth knowledge of the drug development processes across all functional areas Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines Excellent organizational and problem solving skills Effective time management skills and ability to manage competing priorities Strong interpersonal skills effective presentation skills Ability to establish and maintain effective working relationships with coworkers, managers [. .. ] good command of English Ability to influence effectively within SPN/ PRP team and project teams including TSL, PL, CL, CRA and the customer IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and [. .. ]
Job am 24.01.2026 bei Neuvoo gefunden
Advanced Resource Managers
Regulatory CMC Consultant
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Responsibilities : Provide advice to clients on quality aspects of
drug development and regulatory requirements, in close collaboration with cross-functional experts from the team. Ensure that the content of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CMC work-packages and documentation are phase appropriate, meet regulatory expectations and enable approval of regulatory submissions. Preparation of quality sections for MAA and BLA/ NDA as well as for IMPD [. .. ] IMPD, BLA/ NDA/ MAA) . Excellent communication and negotiation skills in English. German language skills are a plus. Experience with CMC and regulatory requirements for all development stages, from pre-clinical to Phase III or commercial. Highly motivated team player with strong interpersonal abilities. Sound knowledge of Microsoft Office applications. Willingness to travel moderately (Meetings with clients, agencies or CMOs) . Disclaimer This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
Infosys Consulting- Europe
Sr. Principal Consultant, Regulatory Strategy and Advisory
• Munich, Bavaria
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 14 offene Stellenanzeigen für Clinical Drug Consultant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Consultant Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Drug Consultant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Drug Consultant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Drug Consultant Stellenangebote:
- Infosys Consulting- Europe (2 Jobs)
- Adragos Pharma GmbH (1 Job)
- IQVIA (1 Job)
- Advanced Resource Managers (1 Job)
- PhD- Jobs. NET (1 Job)
In welchen Bundesländern werden die meisten Clinical Drug Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Consultant Jobs werden derzeit in Bayern (5 Jobs), Hessen (2 Jobs) und Sachsen-Anhalt (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Consultant Jobs?
Clinical Drug Consultant Jobs gehören zum Berufsfeld Pharmazie.
