16 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 [...]
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 gestern bei Jobleads gefunden
• Berlin
When our values align theres no limit to what we can achieve. At Parexel we all share the same goal to improve the worlds health. From
clinical trials to regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] consulting and market access every clinical development solution we provide is underpinned by a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work [. .. ] German and English is essential. An advanced ability to speak and read Polish is also preferred. Responsibilities Negotiate and maintain Clinical Trials Agreements (CTA) , site budgets, Confidential Disclosure Agreements, Consultant Agreements and other applicable contracts. 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. Ensure compliance of contracts with Fair Market Value (FMV) principles and guidelines. Track contract progress, complete required followups [. .. ] 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 daytoday activities related to clinical contracts and budgets as requested. Requirements 35 years experience in the pharmaceutical or biotechnology industry in clinical site contracts and/or outsourcing management. Proficient with Excel and Power Point. Excellent verbal, written [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA
Consultant to support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality processes for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study quality-related plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 2-3 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
GCP QA Consultant
Beratungs-/ Consultingtätigkeiten
[. .. ] message the job poster from Proclinical Staffing Connecting top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] GCP QA Consultant to support quality assurance activities for oncologyfocused clinical trials. This role involves overseeing quality processes for phase 23 studies, ensuring compliance with ICHGCP and regulatory requirements, and managing riskbased quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities Develop and oversee study qualityrelated plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 23 trials, focusing [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Beratungs-/ Consultingtätigkeiten
[. .. ] among the first 25 applicants Direct message the job poster from R D Partners Empowering consultancies, biotech, and pharma companies to scale highperforming HTA/ RWE teams with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategic recruitment solutions. Consultant Shape the future of clinical trials by driving Patient Reported Outcomes strategies that meet global standards and deliver realworld impact. R D Partners is seeking a skilled PRO Consultant to provide expertise in Patient Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment [. .. ] requirements. Please note that to be considered for this role you must have the right to work in this location. Responsibilities Recommend PRO endpoints, instruments, and assessment schedules tailored to trial populations and strategic goals. Review statistical analysis plans for PROs to ensure alignment with protocoldefined endpoints. Collaborate with HEOR Asset Leads to refine PRO strategies based on evidence generation needs. Contribute to Health Technology Assessment (HTA) interactions as required. Key Skills and Requirements Minimum of 5 years of experience in [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• München, Bayern
Vacancy Scientific Informatics Business Analyst Location Munich Hours Full-time The
Consultant will support strategic projects primarily for pharmaceutical and Biotech clients. The Consultant will gather business requirements, analyse customer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs and gaps to propose solutions for the desired state. He or she will interface with business users and client managers in conjunction with the internal Zifo support team. Core Responsibilities As [. .. ] have demonstrated the ability to gain the trust of customers. Thorough understanding in one or more of the following areas of the bio/ pharmaceutical industry Drug discovery and development processes Clinical trial design and data management Laboratory workflows Chemical biologics materials management Sample management Robotic systems integration and qualification Operations KPI and metrics tracking. Be knowledgeable about relevant Regulations and standards that govern the development of technical solutions such as GLP, GMP, 21 CFR Part11, Part210, Part820 regulations. Technical Skills Be familiar [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Bonn, Nordrhein- Westfalen
Homeoffice möglich
[. .. ] function Other Industries IT Services and IT Consulting Referrals increase your chances of interviewing at adesso SE by 2x Sign in to set job alerts for Summer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Staff roles. Freelance Clinical Trial Site Coordinator Cologne, North Rhine-Westphalia, Germany 1 week ago Trainee-Programm Financial Consultant (BWL, Finanzen, VWL) (w/m/d) Cologne, North Rhine-Westphalia, Germany 5 days ago Pedagogical specialist-elementary school child care Cologne, North Rhine-Westphalia, Germany 1 day ago Working Student Finance Procurement (m/f/x) Cologne, North Rhine-Westphalia, Germany 1 day ago Cologne, North Rhine-Westphalia, Germany 3 days [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Executive Director, Oncology Early
Clinical Development Lead Join to apply for the Executive Director, Oncology Early Clinical Development Lead role at GSK. GSK aims to positively impact the health of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2.5billion people by the end of the decade, focusing on vaccines and medicines that address patients needs with the highest probability of success. Position [. .. ] programs, delegating to and interfacing closely with appropriate physicians when needed. Drive endtoend clinical development strategy and alignment to target medicine profiles (TMP) and integrated evidence plans (IEP) , spanning trial design, execution, interpretation, and delivery of results. Lead clinical development discussions and regulatory interactions, drafting clinical components of submissions (IND, NDA, BLA, MAA) and addressing regulator questions. Act as the single Clinical Development accountability within Medicine Development Team (MDT) , Early Development Team (EDT) , and crossfunctional partnerships with Medical [. .. ] presentations, and manuscripts for accuracy and compliance. Lead preparation of clinical sections of regulatory filings (IND, study reports, NDA, annual reports, etc. ) . Provide clinical support for investigator and consultant meetings (e. g. , investigator meetings, advisory boards) . Present study results and translational insights to senior management, scientific advisory boards, regulatory agencies, and other stakeholders. Integrate input from research, clinical, medical, scientific, commercial, regulatory, and manufacturing disciplines to ensure alignment and execution of translational research initiatives. Build and maintain [. .. ]
Job am 05.12.2025 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 04.12.2025 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] currently 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 am 09.10.2025 bei Jobleads gefunden
Teamleiter (w/w/d) Digital Data Management Excellence
• 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
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 vor 2 Tagen bei Neuvoo gefunden
Proclinical
GCP QA Consultant
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA
Consultant to support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] processes for phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to candidates located anywhere within Europe. Responsibilities: Develop and oversee study quality-related plans, including Oversight Quality and Audit Plans. Collaborate with third parties to formalize Investigator Site Audits (ISA) and agendas. Oversee quality activities for phase 2-3 [. .. ]
Job vor 5 Tagen bei Neuvoo.com gefunden
R D Partners
PRO Consultant
• Stuttgart
Beratungs-/ Consultingtätigkeiten
Shape the future of
clinical trials by driving Patient-Reported Outcomes strategies that meet global standards and deliver real-world impact. R D Partners is seeking a skilled PRO
Consultant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to provide expertise in Patient-Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment with strategic objectives and regulatory requirements. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Recommend PRO endpoints, instruments, and assessment schedules tailored to trial populations and strategic goals. Review statistical analysis plans for PROs to ensure alignment with protocol-defined endpoints. Collaborate with HEOR Asset Leads to refine PRO strategies based on evidence generation needs. Contribute to Health Technology Assessment (HTA) interactions as required. Key Skills and Requirements: Minimum of 5 years of experience [. .. ]
Job vor 10 Tagen bei Neuvoo gefunden
Zifo RnD Solutions
Scientific Informatics Business Analyst
• Munich, Bavaria
Vacancy Scientific Informatics Business Analyst Location Munich Hours Full-time The
Consultant will support strategic projects primarily for pharmaceutical and Biotech clients. The Consultant will gather business requirements, analyse customer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs and gaps to propose solutions for the desired state. He or she will interface with business users and client managers in conjunction with the internal Zifo support team. Core Responsibilities: As [. .. ] have demonstrated the ability to gain the trust of customers. Thorough understanding in one or more of the following areas of the bio/ pharmaceutical industry: Drug discovery and development processes Clinical trial design and data management Laboratory workflows Chemical biologics materials management Sample management Robotic systems integration and qualification Operations KPI and metrics tracking. Be knowledgeable about relevant Regulations and standards that govern the development of technical solutions such as GLP, GMP, 21 CFR Part 11, Part 210, Part 820 regulations. Technical [. .. ]
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 16 offene Stellenanzeigen für Clinical Trial Consultant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Consultant Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Clinical Trial Consultant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Consultant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Consultant Stellenangebote:
- Proclinical (1 Job)
- R D Partners (1 Job)
- Zifo RnD Solutions (1 Job)
- PhD- Jobs. NET (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Consultant Jobs werden derzeit in Berlin (3 Jobs), Bayern (2 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Consultant Jobs?
Clinical Trial Consultant Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
