13 Jobs für Clinical Trial Consultant
Stellenangebote Clinical Trial Consultant Jobs
Job am 03.07.2025 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 [...]
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[...] 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/or [. .. ] 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 3 Std. bei Jobleads gefunden
Beratungs-/ Consultingtätigkeiten
[. .. ] AI training. Write fluently in both German and English, ensuring accurate terminology and nuanced expression across languages. Provide cultural and medical insights specific to German healthcare, ensuring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] linguistic accuracy in clinical and professional contexts. Collaborate closely with reviewers and peers to refine content, ensuring high-quality outputs. Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have: Nativelevel fluency in German with strong written and spoken English. Advanced degree (MD or Ph D in a related healthcare [. .. ] Complete an AIled interview to assess language ability and professional experience (15 minutes) . If selected, take a followup AIled interview to assess your professional background. Complete a paid work trial to determine if this type of work is suited for you. Receive feedback and be onboarded to the project. Resources Support For details about the interview process and platform information, please check: https:/ / talent. docs. mercor. com/welcome/ welcome For any help or support, reach out to: PS: Our [. .. ]
Job gestern bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
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[...] 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 and [. .. ] 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 of a Data and Safety Monitoring Committee. As approved, participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication. May participate as high [. .. ]
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 [. .. ] arrange meetings, prepare agendas, and meeting planning. Submit purchase requisitions, where needed, through SAP systems. Support the development and maintenance of guidelines, training programs, policies and procedures related to clinical trial contracts and budget. Support the Director and team in the management of other day-to-day activities related to clinical contracts and budgets as requested. We expect from you 3 5 years experience in the pharmaceutical or biotechnology industry in clinical site contracts and/or outsourcing management. Fluent German, Polish [. .. ]
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 [. .. ] 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 global [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
• München, Bayern
Principal Sourcing Specialist Syneos Health Contract Specialist hybrid in Munich Syneos Health is a leading fully integrated biopharmaceutical solutions organization that accelerates customer success. It translates unique
clinical, medical affairs [...]
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[...] and commercial insights into outcomes to address modern market realities. The companys clinical development model places the customer and the patient at the centre of everything it does, continually simplifying work to make Syneos Health easier to work with and to work for. Whether you join us in [. .. ] to accelerate the delivery of therapies because we are passionate about changing lives. Job Responsibilities Administers all contract management processes, including coordination with relevant protocol, informed consent, institution, investigator, vendor, consultant, and customer agreement documents at a project level. May lead (with supervision) multicountry projects including negotiating and preparing contracts, budgets, and related documents for participation in industrysponsored clinical trials. Provides support to SSUL to agree on country template contract and budget. Produces sitespecific contracts from country template. Provides support in [. .. ] of the clinical development process and legal and contracting parameters. Customerfocused and ability to manage challenging priorities and to remain flexible and adaptable in stressful situations. Excellent understanding of clinical trial process across phases IIIV and ICH GCP. Good understanding of clinical protocols and associated study specifications. Excellent understanding of clinical trial startup processes. Project management experience in a fastpaced environment. Good vendor management skills. Excellent written/ oral communication, presentation, documentation, interpersonal skills as well as strong teamorientation. Strong organizational skills [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
• München, Bayern
Firmenwagen Betriebliche Altersvorsorge
Consultant-Medical Devices I US Europe I Electrophysiology Mapping Cardiology I Neurology Vascular Interventions Territory Support Specialist Munich (Structural Heart/
Clinical Specialist) Therapy Area: Structural Heart Transcatheter Valve Therapies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] About the Opportunity Were representing a fast-growing Med Tech innovator in the structural heart field, developing nextgeneration transcatheter valve technologies that are transforming the treatment of aortic regurgitation and valve disease. As a Territory Support Specialist, youll work closely with physicians [. .. ] Collaborate with the regional sales and therapy team to drive therapy awareness and adoption. Act as a technical and clinical expert, supporting case planning, troubleshooting, and postprocedure followup. Support clinical trial activities and data collection when required. About You Background as a Cardiac Physiologist, Cath Lab Nurse, Field Clinical Specialist, or similar clinical support role. Experience in structural heart, TAVR/ TAVI, or complex interventional cardiology preferred. Excellent communication and relationshipbuilding skills with hospital stakeholders. Fluent in German and English. Based in [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen Abgeschlossenes Studium
[. .. ] LKQ STAHLGRUBER by 2x Get notified about new Teamleiter (w/w/d) Digital Data Management Excellence jobs in Greater Munich Metropolitan Area. (Senior) Business Development Manager (m/f/x) Senior
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[...] class=highlight_text>Consultant (m/f/d) - Allianz Consulting-Strategic Initiatives Change Senior Investor Relations Manager (all genders) HR EHS Communication and Change Lead (flexible location within Europe)
Clinical Trial Manager-Early Phase (f/m/d) Team Lead Transaction Management (m/f/d) Strategic Controller (inc. M A and Ventures) Product Lead, Supply Chain (Order Management) Senior Consultant Digital Acceleration (m/w/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with [. .. ]
▶ Zur Stellenanzeige
Job am 31.08.2025 bei Jobleads gefunden
VP Pathology (m/f/d)
• Kassel, Hessen
[. .. ] 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/or [. .. ] 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 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 increased patient access to medicines Accelerated regulatory approval Responsibilities Our Pharmacometricians are responsible for supporting quantitative decision-making in drug development through the development and application of population PK, PK/ PD, exposure-response and other models. Qualified candidates will have the ability [. .. ] 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 15.09.2025 bei Job-Consult gefunden
PhD- Jobs. NET
Specialist Radiology/ Mammography
• Norway/ sonstiges/ Europa
specialist radiology mammography phd jobs net norway a vacancy as a staff specialist
consultant in radiology mammography is open at a hospital in the south of norway the position [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is divided between breast diagnostics and general radiology the department has ca employees at the breast diagnostics center its performed relatively many cytologic exams of thyroid us guided about per normal week and biopsies of breast axilla up to per week tasks screening activity and clinical activity with the extensive use of the intervention endocrine imaging in form of ultrasound thyroid and ultrasound guidance fnac general radiology with planned and emergency operations requirements specialist title in radiology with experience and or special interest in breast diagnostic availability to complete the norwegian intensive course our offer permanent contract after a six month trial period salary starting from gross duties if there will be will be paid apart training courses within working hours help to find apartment school and kindergarten invitation to study tour to norway after a first interview to learn more about the region and the work environment assistance with removal and [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Consultant pro Jahr?
Als Clinical Trial Consultant verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 13 offene Stellenanzeigen für Clinical Trial Consultant Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Consultant Jobs werden derzeit in Bayern (3 Jobs), Sachsen-Anhalt (3 Jobs) und Hessen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Consultant Jobs?
Clinical Trial Consultant Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
