31 Jobs für Clinical Trials Specialist
Stellenangebote Clinical Trials Specialist Jobs
Job am 24.08.2025 bei Mindmatch.ai gefunden
Bristol Myers Squibb
• AT- 9 Wien
Join to apply for the Therapeutic Area
Specialist, Oncology (m/w/d) - Westösterreich (Salzburg, Tirol, Vorarlberg) role at Bristol Myers Squibb 2 days ago Be among the first 25 applicants Join [...]
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[...] to apply for the Therapeutic Area Specialist, Oncology (m/w/d) - Westösterreich (Salzburg, Tirol, Vorarlberg) role at Bristol Myers Squibb Working with Us Challenging. Meaningful. [. .. ] ability to think strategically, drive performance, foster customer relationships and build alignment positive working relationships through a strong cross-functional collaboration. Good scientific understanding with the ability to simplify complex clinical data to concise and convincing messages Solution-oriented can-do mentality and ability to work effectively in complex, rapidly changing environment Open to new technologies and digital ways of working Good organizational skills, along with the ability to work on multiple tasks, and to effectively prioritize Strong motivation to continuously [. .. ] role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-[. .. ]
Job gestern bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
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[...] resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, [. .. ] Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions : Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement : Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications : Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise : Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge : Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation and internal SOPs. Adaptability : Comfortable working in fast-[. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
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[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with [. .. ]
Job gestern bei Jobleads gefunden
Site Budget Contract Specialist
• München, Bayern
Site Budget Contract
Specialist Fortrea Join to apply for the Site Budget Contract Specialist role at Fortrea. Be among the first 25 applicants. Principal Talent Acquisition Partner DACH at Fortrea/ [...]
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[...] Driving Data-Driven Talent Strategies/ Stakeholder Engagement/ DEI Advocate Join Our Team and Shape the Future of Clinical Research At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget Contract Specialist, you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Wien
Homeoffice möglich
[. .. ] we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. [...]
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[...] The Position The Clinical Trial Information System Team (part of Product Development Regulatory Operations) enables the development of organizational and people capabilities of the future, we support and optimize the delivery of projects and initiatives to the organization both on the molecule and molecule-enabling portfolio. We are responsible for enabling the future of clinical trials from a regulatory perspective by pushing boundaries to deliver medical solutions now in order to transform patients lives. Please note that this is a fixed term position for 1 year. The Opportunity: As a CTIS-team Specialist, you will manage the administration of the EU CTA CTIS User Management Create initial CTAs as well as any other post-approval activities during the whole CTA lifecycle (e. g. modifications, inclusion of additional countries) in CTIS: Support compilation submission activities as per defined process and instructions from relevant functions [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Regulatory And Clinical Start Up Specialist (Biotech)
• München, Bayern
Regulatory And
Clinical Start Up
Specialist (Biotech) Join to apply for the Regulatory And Clinical Start Up Specialist (Biotech) role at Progressive Direct message the job poster from [...]
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[...] Progressive Regulatory and Start up Associate/ Specialist Responsible for oversight of assigned global clinical trials Review of regulatory submission documents and packages Support study teams as RA representative Preparation of responses to regulatory requests Support of regulatory interactions as applicable Negotiation of Budgets Contract Management Experience Requirements University degree or professional education e. g. Pharmaceutical/ Medical Technical Assistant with a minimum of 1-2 years [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] for tardive dyskinesia, chorea associated with Huntingtons disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid-to [...]
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[...] late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, [. .. ] opportunities for marketed products. Your Contributions (include, but are not limited to) : Oversight of the clinical development strategy in the endocrinology therapeutic area Oversight of the design of clinical trials across early to late-stage development to ensure they meet regulatory requirements and scientific standards Lead the writing of protocols and major amendments, design of data collection systems, and preparation of clinical study reports, engaging with external experts as needed Collaboration with Clinical Operations to ensure trials are implemented in [. .. ] of data and identification of evidence generation needs Adhere to Neurocrine Europe quality assurance system and compliance with the relevant SOPs Requirements: The appointed candidate will be a physician with specialist experience/ qualifications in endocrinology and/or a proven track record of clinical development in endocrinology products. MD qualified, ideally with specialist medical qualification in Endocrinology and previous experience in patient care At least 8 years experience in early or late stage clinical development in the pharmaceutical industry, ideally including experience [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Senior Field Medical Specialist-Region West-Mainz, Köln, Düsseldorf (m/w/d)
Overview Join to apply for the Senior Medical Affairs
Specialist-Region West-Mainz, Köln, Düsseldorf (m/w/d) role at Dexcom. Dexcom Corporation (NASDAQ: DXCM) is a pioneer and a global leader in [...]
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[...] continuous glucose monitoring (CGM) . We aim to improve human health by providing accessible information and insights that lead to better health outcomes. Our future is to [. .. ] millions of lives and are ready to change millions more. This position is focused on medical affairs activities in the region, bridging the company with healthcare professionals (HCPs) and supporting clinical strategy, product development and educational activities. Position Summary The Field Medical Science Specialist/ Medical Affairs Specialist acts as the bridge between the company and healthcare professionals (HCPs) , providing in-depth scientific knowledge, practical medical applications and support for our products and research. The FSS is the medical and scientific [. .. ] updates on current research and clinical practices during product launches, customer meetings and training sessions. Clinical Research Support Support the clinical research teams to identify sites and investigators for clinical trials. Data Dissemination and Insights Gather information from KOLs on how they are using our products. Provide feedback to marketing and sales to help develop marketing materials and commercial strategy. Represent the company at scientific conferences, meetings, and advisory boards, communicating data and engaging in scientific discussions. Compliance and Reporting Ensure [. .. ]
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, [...]
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[...] medical affairs 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 [. .. ] 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 submissions for proposed contract and budget for site. Provides support in negotiating budget and contract with site via Site Contracts Service Centre and SSUL with Sponsor until resolution of [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
Data Analytics Manager Data Technology, SCD
• Liestal, Basel- Landschaft
[. .. ] later than 26th of October 2025. For more information about the position please contact Data Technology Manager Fredrik Larsson at. For questions regarding the recruitment process please [...]
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[...] contact People Culture Specialist Katie Pettersson at. At IKEA we believe that were better when were physically together for collaboration dialogues and conversations. We believe in the power of human interactions; the informal chats the energy belonging and creativity generated by people being in the same place. Our approach is that we spend majority [. .. ] IKEA workplace and with flexibility to work from home when relevant. Remote Work: No Employment Type: Full-time Key Skills SQL, Data Collection, GCP, Master Data Management, R, Data Management, Clinical Trials, User Acceptance Testing, Data Warehouse, SAS, Oracle, Data Analysis Skills Experience: years Vacancy: 1 #J-18808-Ljbffr 68370745 [. .. ]
Job am 18.10.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] Compliance Position Purpose Member of the Trial Risk and Integrity Management (TRIM) department within Trial Delivery Support. Responsible for executing a comprehensive and integrated Quality Risk Management [...]
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[...] (QRM) program across clinical operations, with a focus on Good Clinical Practice (GCP) guideline compliance. Responsible for identifying and mitigating emerging business risks using advanced risk assessment principles and methodologies, including quality and performance analytics, for thorough mitigation, continuous monitoring and oversight. Foster and promote a culture of Quality Excellence and Inspection Readiness, building [. .. ] principles and demonstrating business benefits to partners and peers. Responsible for monitoring GDO performance by assessment of compliance and quality trends, using QMS and associated system and platform datasets. Data specialist with fluency in clinical data analytics, interpretation and trend discovery to support evidence-based decision-making and continuous performance monitoring. Risk Management specialist, applying advanced principles and techniques to proactively identify, assess, and mitigate risks across clinical operations Responsible for assigning priority and escalating risks as appropriate Responsible for maintaining [. .. ] role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-[. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Clinical Trial Assistant/ Clinical Research Associate (m/w/d) , Delhi, India
• Dresden, Sachsen
[. .. ] Manager Medical Imaging (m/f/d) Full-time permanent hybrid Our young, dynamic, and continuously growing team is looking for new colleagues whether you are a fresh talent, an experienced [...]
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[...] specialist, or simply at home in the world of medical imaging. ABX-CRO is an internationally operating contract research organization (CRO) headquartered in Dresden. We provide worldwide services in the manufacturing, testing, and approval of pharmaceuticals and diagnostics. Within the Image Core Lab, we handle all aspects of medical image processing in the context of clinical trials. Your Tasks Responsibilities Planning and coordination of clinical trials with multimodal imaging Organization of image processing and data evaluation Further development and optimization of our imaging workflows Collaborating in an international team on equal footing About You Completed degree or comparable qualification Strong command of English Knowledge of medical imaging [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Jobticket
Join to apply for the
Specialist Global Regulatory Affairs role at Bio NTech SE Mainz, Germany full time You will support the Global Regulatory Affairs (GRA) Development Pipeline team [...]
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[...] in the planning, preparation, and recording of regulatory submissions. In your role you will closely work with the Global Regulatory Leads (GRLs) in managing clinical trials and product development from a regulatory perspective. Moreover, you may act as the primary contact for local regulatory partners or collaborators (e. g. license partners, affiliates, local regulatory vendors, CROs) . Your main responsibilities are: Prepare regulatory documentation in close cooperation with the GRL and GRA internal and external stakeholders [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Global Medical Affairs Director, Autoimmune Diseases
Führungs-/ Leitungspositionen
[. .. ] with post-market solutions, including medical affairs planning and execution of the medical/ scientific engagement strategy. They address and deliver strategic pre-launch and launch medical activities needs for [...]
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[...] patient, clinical, access and value to health care systems. Providing expertise in the development and execution of the overarching strategies and providing inputs during design and along the end-to-end execution of programs. About The Role The Global Medical Affairs (GMA) team acts as enterprise medical voice across the asset lifecycle [. .. ] for promotional and non-promotional global materials; deputise for the Executive Medical Director across PMAT/ GCT/ GPT, regional alignment, internal decision boards and external activities. Essential Requirements: Medical Degree (MD) Specialist Degree or specialist qualification related to Rheumatology. 5+ years in Pharmaceutical Industry with experience in Medical Affairs at global level and/or Clinical Development Firm working knowledge of Clinical Trials, including Good Clinical Practice (GCP, ) scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities Deep understanding of health care systems and key external stakeholders Critical thinker, agile mindset, ability to navigate uncertainty without major supervision, ability to truly collaborate [. .. ]
Job am 02.10.2025 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] with post-market solutions, including medical affairs planning and execution of the medical/ scientific engagement strategy. They address and deliver strategic pre-launch and launch medical activities needs for [...]
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[...] patient, clinical, access and value to health care systems. Providing expertise in the development and execution of the overarching strategies and providing inputs during design and along the end-to-end execution of programs. They also develop and execute the Integrated Evidence Plan (IEP) / functional specific programs to maximize the value [. .. ] for promotional and non-promotional global materials; deputise for the Executive Medical Director across PMAT/ GCT/ GPT, regional alignment, internal decision boards and external activities. Essential Requirements Medical Degree (MD) Specialist Degree or specialist qualification related to Rheumatology. 5+ years in Pharmaceutical Industry with experience in Medical Affairs at global level and/or Clinical Development Firm working knowledge of Clinical Trials, including Good Clinical Practice (GCP) , scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities Deep understanding of health care systems and key external stakeholders Critical thinker, agile mindset, ability to navigate uncertainty without major supervision, ability to truly collaborate [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
Senior Statistical Programmer (Home-Based, anywhere in Europe)
[. .. ] anywhere in Europe) Hobson Prior is seeking a Senior Statistical Programmer to join our clients team. This is a remote role anywhere within Mainland Europe. This role [...]
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[...] focuses on supporting clinical activities in oncology and rare disease trials. You will be responsible for developing statistical reports and datasets while managing outsourced tasks. You will also lead projects to ensure timely and high-quality results and maintain positive collaborations. Responsibilities: Develop statistical reports and datasets. Manage outsourced data tasks. Lead projects to ensure quality and timeliness. Collaborate effectively with [. .. ] more or applying to this exciting opportunity, please click Apply and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please select Contact me at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. #J-18808-Ljbffr [. .. ]
Job am 01.07.2025 bei Jobleads gefunden
• München, Bayern
Clinical Trial Site Relationship Coordinator Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations [...]
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[...] team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain [. .. ] responsibilities as assigned, including site Qualification Visits, prepping/ consultation support for site audits, etc. Qualifications Minimum a Bachelor of Science in health-related field; Minimum 1 years site and clinical trials experience (more experience for the more senior positions required) ; CRA experience is an asset; Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred; Knowledge of medical terminology and clinical patient management preferred; Fluency in English; German; Demonstrated organizational and prioritization skills; Excellent oral and [. .. ] type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Medpace by 2x Clinical Trial Associate/ Specialist (CTA/ CTS) Freelance Clinical Trials Site Coordinator Sponsor Dedicated Clinical Trial Assistant in Munich area Senior Clinical Research Associates (experienced) - Germany (Senior) Research Manager-Spine Neurosurgery Expert Clinical Trials Statistics and Programming Working Student-Clinical Data Processing (m/f/d) Were unlocking community knowledge in a new way. Experts [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Leipzig
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
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[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
• Essen
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Düsseldorf Duesseldorf
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Berlin
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Frankfurt
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Stuttgart
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Cologne
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Planet Pharma
Senior Clinical Research Associate
• Hamburg
Senior CRA Germany Therapeutic Area: Cell Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior
Clinical Research Associate to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies. You will play a key role in overseeing complex clinical trials, ensuring high-quality monitoring, and driving operational excellence across German study sites. This is an opportunity to work at the cutting edge of science, supporting transformative therapies that have the potential to redefine treatment outcomes for patients with severe and rare diseases. Key Responsibilities Perform independent on-site and remote [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Specialist pro Jahr?
Als Clinical Trials Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 31 offene Stellenanzeigen für Clinical Trials Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Specialist Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Trials Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Specialist Stellenangebote:
- Planet Pharma (11 Jobs)
- Bristol Myers Squibb (1 Job)
- Parexel (1 Job)
- Medpace (1 Job)
- Recruiter Vitaly Pryadka (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Specialist Jobs werden derzeit in Bayern (5 Jobs), Nordrhein-Westfalen (4 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Specialist Jobs?
Clinical Trials Specialist Jobs gehören zum Berufsfeld Pharmazie.
