11 Jobs für Clinical Trials Consultant
Stellenangebote Clinical Trials 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 [. .. ] 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 an [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Schwyz
Beratungs-/ Consultingtätigkeiten
Go back Cambridgeshire and Peterborough NHS Foundation Trust
Consultant Psychiatrist in Community Old Age Psychiatry-Fenland The closing date is 25 February 2026 The successful candidate will work alongside a community-based [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] colleagues to provide assessment and psychiatric treatment for Older Adults within the Fenland community across a largely rural area. The population of over 65s in the Fenland [. .. ] psychiatry outpatient and 36 for memory assessment. Salary 109, 725-145, 478 per annum plus 40, 000 Recruitment and Retention Premium (T Cs apply) . Main duties of the job Clinical: To lead the multidisciplinary team in providing excellent psychiatric care. To provide assessment, diagnosis, and treatment plans. To lead weekly MDT meetings and ensure prompt reviews of acutely unwell patients. To work closely with the CRHTT OP, community teams and liaison services as patients move between these teams. Cambridgeshire offers [. .. ] CPFT research endeavour where possible. It is anticipated that funding would become available for the right applicant to become involved in research, potentially acting as a principal investigator for clinical trials into dementia and other late life mental health disorders or making use of local opportunities to develop other research interests. Clinical Governance The post-holder will be aware of, and act within, locally and nationally agreed protocols and actively involved in clinical governance within the service. On-call The post [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
• Kassel, Hessen
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 compensation packages that are market [. .. ]
Job am 14.01.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
Position: Brand Ambassador/ Cryptocurrency Analytics
Consultant Location: Your City Germany (On-site) About the Company: Assetara Limited is a global leader in AI-powered financial analytics and trading solutions. We are committed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to innovation excellence and expanding our presence across Asia Europe and the USA through a dynamic and client-focused team. Job Brief We are [. .. ] your city of residence in the USA. How to Apply Submit your resume and a brief cover letter through our career page or email. Key Skills Fundraising Management Experience Biotechnology Clinical Development Clinical Trials Research Development Training Development Grant Writing Economic Development Leadership Experience Public Speaking Product Development Employment Type Full Time Experience years Vacancy 1 Monthly Salary Salary 1000-10000 #J-18808-Ljbffr 74646821 [. .. ]
Job am 13.01.2026 bei Jobleads gefunden
• Dortmund, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
What Youll Do Qserve is seeking a
Consultant Clinical Affairs with strong medical writing skills and expertise in systematic literature searching and clinical evaluation of medical devices. In this role, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will support clients in navigating complex regulatory landscapes for devices of different risk classes. You will work closely with global experts to ensure compliance and market access for [. .. ] clinical outcome parameters and acceptance criteria to support the clinical claims of the devices. Perform design and appraisal of systematic literature searches on multiple databases (Pub Med, Science Direct, Clinical Trials and others) , including adverse event ones, such as MAUDE, FDA Medical Device Recalls and similar. Elaborate, update and peer review Clinical Evaluation Plans (CEPs) , Clinical Evaluation Reports (CERs) and Literature Search Reports (LSRs) . Write stateoftheart (SOTA) text based on selected data. Ensure that peer review of any [. .. ]
Job am 13.01.2026 bei Jobleads gefunden
Consultant Clinical Affairs
• Köln, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
What Youll Do Qserve is seeking a
Consultant Clinical Affairs with strong medical writing skills and expertise in systematic literature searching and clinical evaluation of medical devices. In this role, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will support clients in navigating complex regulatory landscapes for devices of different risk classes. You will work closely with global experts to ensure compliance and market access for [. .. ] clinical outcome parameters and acceptance criteria to support the clinical claims of the devices. Perform design and appraisal of systematic literature searches on multiple databases (Pub Med, Science Direct, Clinical Trials and others) , including adverse event ones, such as MAUDE, FDA Medical Device Recalls and similar. Elaborate, update and peer review Clinical Evaluation Plans (CEPs) , Clinical Evaluation Reports (CERs) and Literature Search Reports (LSRs) . Write stateoftheart (SOTA) text based on selected data. Ensure that peer review of any [. .. ]
Job am 12.01.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Homeoffice möglich
[. .. ] f/d) . Background We are looking for a Senior Solution Architect with strong expertise in data processing systems to design and implement a large-scale sensor data platform [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for clinical trials. In this role, you will create technical architectures, documentation, and collaborate closely with project leadership and engineering teams to ensure successful execution. The ideal candidate brings around 8 years of architecture experience, solid AWS knowledge, Python skills for automation or prototyping, and excellent English communication abilities. General Information Start date: [. .. ] Have: Compliance Awareness: (Nice-to-have) Experience working in regulated environments such as Sa MD (Software as a Medical Device) or CSV (Computer System Validation) Contact Jan Schmitz-Elsen Talent Acquisition Consultant +41 61 50001 74 We look forward to receiving your online application with your CV Find more vacancies at: #J-18808-Ljbffr 74556297 [. .. ]
Job am 12.01.2026 bei Jobleads gefunden
Consultant Clinical Affairs
• Essen, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
What Youll Do Qserve is seeking a
Consultant Clinical Affairs with strong medical writing skills and expertise in systematic literature searching and clinical evaluation of medical devices. In this role, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will support clients in navigating complex regulatory landscapes for devices of different risk classes. You will work closely with global experts to ensure compliance and market access for [. .. ] clinical outcome parameters and acceptance criteria to support the clinical claims of the devices. Perform design and appraisal of systematic literature searches on multiple databases (Pub Med, Science Direct, Clinical Trials and others) , including adverse event ones, such as MAUDE, FDA Medical Device Recalls and similar. Elaborate, update and peer review Clinical Evaluation Plans (CEPs) , Clinical Evaluation Reports (CERs) and Literature Search Reports (LSRs) . Write stateoftheart (SOTA) text based on selected data. Ensure that peer review of any [. .. ]
Job am 25.12.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
Clinical Applications Specialist Join to apply for the Clinical Applications Specialist role at Tera Recon, Inc. Company Overview Concert AI is at the forefront of revolutionizing healthcare with our cuttingedge [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] AI and data solutions. Our mission is to accelerate insights, advance research, and improve patient outcomes in oncology and across life sciences. [. .. ] solution provider for AIempowered radiology, oncology, cardiology, neurology, and vascular surgery. In the future, the combination with Concert AI could bring a single, advanced AIaugmented diagnosis and interpretation capability from clinical trials to patient care. Learn more about Tera Recon at, or follow us on Linked In. EEO Concert AI provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected [. .. ]
Job am 16.12.2025 bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Position title (Senior)
Consultant, Qualified Person Description Granzer Pharmaceutical Services Gmb H was founded in 2022 as a spin-off of Granzer Regulatory Consulting Services Gmb H. We are a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Pharmaceutical Service Provider and Consultancy for the Development, Manufacturing and Quality Assurance of Medicinal Products. Our focus is the EU Import, Storage, Distribution and EU-Release of Investigational Medicinal Products, supporting the Clinical Trials of our Clients. For our team in Munich, we are looking for a (Senior) Consultant, Qualified Person Responsibilities Act as (deputy) Qualified Person under Granzers manufacturing authorisation Provide expertise and consulting on GMP-related items to our clients Support the import and batch release processes for client products Perform GMP/ [. .. ]
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 [. .. ] 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 [. .. ] meta-analysis, dose-response and exposure-response analyses, dataset creation, disease modeling, trial simulation, optimal study designs, strategic decision analyses, economic modeling) . Experience in moving compounds through the clinical trials process and experience with various elements of clinical development and trial design and management and filings preferred. Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Consultant pro Jahr?
Als Clinical Trials Consultant verdient man zwischen EUR 50.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 11 offene Stellenanzeigen für Clinical Trials Consultant Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Consultant Jobs werden derzeit in Nordrhein-Westfalen (3 Jobs), Bayern (2 Jobs) und Hessen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Consultant Jobs?
Clinical Trials Consultant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
