80 Jobs für Clinical Trials Associate
Stellenangebote Clinical Trials Associate Jobs
Job vor 7 Tagen bei Jobleads gefunden
• Wien
[. .. ] operational support activities as assigned. Your expertise and ideal skill set Medical-pharmaceutical or scientific university degree. At least 5 years of experience in clinical research. Previous experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a Clinical Trials Associate/ Assistant, Clinical Research Associate or similar. Knowledge of the pharmaceutical industry or CRO industry and of the global clinical trials environment. Solid experience with Phase 2 or 3 studies and good IT skills. Proficient in English (written and oral) ; additional languages beneficial. Strong interpersonal communication and organisational skills. Ability [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• AT- 9 Wien
Homeoffice möglich
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research
Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate [. .. ] Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to apply MDR, ISO 14155 and ICH/ GCP guidelines governing clinical trials. Strong compliance focus. Demonstrated aptitude and knowledge in relevant therapeutic areas and ability to learn and integrate new therapeutic areas knowledge. Ability to train and mentor Clinical Studies personnel for remote and onsite monitoring visits. Ability to train onsite staff on the protocol, GCPs, data entry and other pertinent regulations. [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
Local Study Associate Director
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Job gestern bei Jobleads gefunden
[. .. ] allows a patients physician time to assess their longterm arrhythmic risk and make appropriate plans. Our mission: Saving more lives Our EMEA team is looking for a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] dedicated and motivated Clinical Research Associate (CRA) to support us in the execution and monitoring of clinical trials. In this role, you will play a key part in ensuring the quality and integrity of our clinical research projects from planning through to implementation. Areas of Responsibility Monitoring and site management activities for clinical research projects Acting as liaison between the company and clinical sites to resolve any siterelated [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Research Associate (m/w/d) - Inklusiver Job
• Schwabenheim an der Selz, Rheinland- Pfalz
We are seeking a
Clinical Research
Associate (m/w/d) to join our team at our innovative research facility in Schwabenheim (near Mainz) . This is a fulltime position on a twoyear [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] fixedterm contract. Main responsibilities Conducting paper and electronic clinical studies under the direction of the Clinical Study Team Leader Supporting the planning, organization and archiving [. .. ] they are equally qualified. Required Skills Adverse Event Report, Clinical Evaluation Reports, Clinical IT, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Good Clinical Data Management Practice (GCDMP) , Good Clinical Practice (GCP) , Investigations Training, Patient Recruitment, Quality Mindset, Regulatory Training #J-18808-Ljbffr 96356931 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Wien
Führungs-/ Leitungspositionen
IQVIA is seeking a Local Study
Associate Director in Vienna, Austria, to lead Local Study Teams ensuring timely data delivery and compliance with international guidelines. Responsibilities include site selection, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] budget management, and overseeing clinical trials. The ideal candidate holds a Bachelors degree with at least 3 years in Development Operations, and possesses strong leadership and project management skills. A competitive salary starting at 58, 500 is offered. #J-18808-Ljbffr 96287658 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Manager Clinical Trial Payments
• Berlin
[. .. ] person is considered as an individual. At Johnson Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function R D Operations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Job Sub Function Clinical Trial Project Management Job Category Professional All Job Posting Locations Beerse, Antwerp, Belgium, Berlin, Germany, Issy-les-Moulineaux, France, Madrid, Spain, Prague, Czechia, Warsaw, Masovian, Poland Job Description Global Clinical Operations (GCO) Manager, Payments (CCS) Position Summary As the Manager, Regional Payments Lead you are responsible to run the local [. .. ] including performance and development (Global team-virtual environment) . Develop talent to enhance the teams effectiveness. Exemplary customer focus with vision to drive solutions. Principal Relationships This position reports to Associate Director, Payments. Internal: Internal Business Partners (CCS, GD, etc. ) External: Clinical Investigator Sites, Commercial Suppliers. Education And Experience Requirements Bachelors degree or equivalent. 7-10 years experience and/or equivalent competencies in pharmaceutical industry/ clinical research. Must have a working knowledge of the clinical payment processing with 4 years [. .. ] well as in a collaborative team environment. Other Fluency in English required. Any additional language is a bonus. Required Skills Analytical Reasoning, Budgeting, Clinical Trial Management Systems (CTMS) , Clinical Trials, Compliance Management, Contract Management, Execution Focus, Fact-Based Decision Making, Laboratory Operations, Mentorship, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Standard Operating Procedure (SOP) , Technical Credibility. Benefits The anticipated base pay range for this position is: In addition to base pay, we offer the following benefits: [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Job Title: Field
Clinical Research
Associate This role supports the Clinical Operations team by overseeing clinical studies, ensuring high-quality human study data collection, and facilitating collaboration between internal [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study teams, contract research organizations, and clinical sites. You will take ownership of site monitoring and study oversight for multiple clinical studies, with a focus on software [. .. ] experience, including handson support for clinical operations. Experience collaborating with contract research organizations and clinical sites to support study execution. Experience facilitating training of site and vendor personnel for clinical trials. Proven track record in tracking and managing regulatory documentation for clinical studies. Experience in analyzing and reconciling clinical study data and generating operational or invoicing reports. Demonstrated ability to monitor clinical sites and ensure adherence to study protocols and regulatory standards. Strong attention to detail to ensure compliance with study [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Principal Scientist/ Associate Director Translational Oncology
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] cross functional organizations. This role is designed for a scientific leader who not only drives cutting edge research but also shapes broader program direction by connecting discovery, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] translational science, and clinical strategy. The successful candidate will play a pivotal role in advancing oncology programs by translating deep biological insights into impactful therapeutic and biomarker strategies, while effectively navigating and influencing a global, matrixed research environment. Job Description Key Responsibilities Define and drive translational research strategies grounded in deep expertise in cancer [. .. ] an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Skills Desired Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Communication Skills, Curious Mindset, Data, Data Analysis, Decision Making, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy-Leadership, Influence, Laboratory, Lifesciences, Machine Learning (ML) , Medical Research, Mentorship + 11 more #J-18808-Ljbffr 96113430 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Lachen, Schwyz
[. .. ] a privately-owned company, where the warmth of family meets the scale of a global organisation. Join us in shaping our vision to provide new health solutions advancing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] human life. Clinical Trial Manager-Central Monitoring Your main tasks and responsibilities Central Data Review Perform ongoing, in-depth review of clinical trial data across multiple studies (e. g. , EDC, IVRS, safety, central laboratory databases) . Identify data inconsistencies, missing data, protocol deviations, and outliers at patient and site level. Cross-Study Oversight Manage simultaneous data review across multiple small trials, ensuring consistency in oversight. Query Management Data Quality Improvement Review and initiate targeted queries for critical or inconsistent data points. Provide clear, actionable feedback to avoid repetitive errors. Protocol Compliance Monitoring Detect protocol deviations through data review. Communication Issue Escalation Act as a central point of contact for data-related [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Associate Director CMC Regulatory
Führungs-/ Leitungspositionen
Job Title:
Associate Director, CMC Regulatory This role leads Chemistry, Manufacturing, and Controls (CMC) regulatory activities with a strong nonclinical focus, supporting faculty and staff on product development and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory strategy. The Associate Director, CMC Regulatory provides expert guidance on regulatory requirements for animal studies and clinical applications, prepares and supports submissions to health authorities, and partners closely with clinical research teams to advance innovative therapies, including gene therapies and biologics. The position offers the opportunity to work as part of an internal clinical research organization, gain broad exposure across multiple therapeutic areas, and contribute to cutting-[. .. ] clinical research units, including compliance, regulatory support, contracting, operations, and finance, to facilitate successful clinical trial execution. Provide internal consultation on regulatory pathways for investigator-initiated and industry-sponsored clinical trials across multiple therapeutic areas. Work independently on assigned projects, managing timelines, deliverables, and communication with stakeholders. Contribute to ongoing education and training initiatives related to regulatory requirements and best practices. Participate in regular internal meetings and training sessions to stay current on evolving regulatory expectations and emerging scientific areas such [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Crans (VD) , Waadt Crans (VD)
[. .. ] technical acumen. Show advanced understanding in a relevant area of scientific expertise, mathematical modelling or statistics. Possess advanced skills in software programming, design, application or usage. Have [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] substantial experience in clinical trial design, coordination and management or in the support services related thereto. Able and willing to work both independently and as a team member. Have a serviceorientated and professional demeanour. Data Scientist SOCAR Research, located in Nyon, Switzerland, is a leading Functional Service Provider with more than 30 years of [. .. ] and good knowledge of global regulatory requirements such as ICH GCP and CFR 21 part 11. Analytical mindset with problemsolving skills. Detailoriented with excellent organizational and communication skills. Clinical Research Associate (CRA) SOCAR Research, located in Nyon, Switzerland, is a leading Functional Service Provider with more than 30 years of experience in the provision of clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. We are seeking an experienced Clinical Research Associate (CRA) . You will be [. .. ] experience) . Minimum of three years experience as a Clinical Research Associate (CRA) . Strong working knowledge and understanding of ICHGCP, Swiss and other international laws and regulations governing clinical trials. Strong medical/ clinical knowledge. Excellent clinical trial monitoring skills with a high level of attention to detail and sound problemsolving skills. Excellent interpersonal communication skills (verbal and written) . Ability to prioritise multiple tasks and achieve project timelines. Computer skills (MS Office) and experience in e CRF systems, CTMS systems, as [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Associate Director Engineering (m/f/d)
Führungs-/ Leitungspositionen
[. .. ] as possible. Without safe, easytouse, highquality drug delivery systems our patients could not get their medicines. This is where you come in; the Device Technology Solution Center [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs you as Associate Director Engineering for the development of drug device combination products working alongside our talented, bright and diverse teams. Our Device Technology Solution Center drives the technical development of autoinjectors as well as novel drug delivery principles, e. g. drug delivery to the brain or radioligand therapy. We closely collaborate with [. .. ] Autoinjectors. Create and maintain relevant Design History File (DHF) documents, ensuring highquality device design and development. Contribute to all phases of medical device development. Ensure components meet quality standards for clinical trials and commercial production. Collaborate with internal and external partners. Identify root causes of issues, define and implement robust solutions. Essential Requirements Degree in mechanical engineering or equivalent. Preferably 10+ years of experience in medical device development. Proficient spoken communication and excellent technical writing skills in English, preferable also German. Proven [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Crans (VD) , Waadt Crans (VD)
[. .. ] technical acumen. Show advanced understanding in a relevant area of scientific expertise, mathematical modelling or statistics. Possess advanced skills in software programming, design, application or usage. Have [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] substantial experience in clinical trial design, coordination and management or in the support services related thereto. Able and willing to work both independently and as a team member. Have a serviceorientated and professional demeanour. Data Scientist SOCAR Research, located in Nyon, Switzerland, is a leading Functional Service Provider with more than 30 years of [. .. ] and good knowledge of global regulatory requirements such as ICH GCP and CFR 21 part 11. Analytical mindset with problemsolving skills. Detailoriented with excellent organizational and communication skills. Clinical Research Associate (CRA) SOCAR Research, located in Nyon, Switzerland, is a leading Functional Service Provider with more than 30 years of experience in the provision of clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. We are seeking an experienced Clinical Research Associate (CRA) . You will be [. .. ] experience) . Minimum of three years experience as a Clinical Research Associate (CRA) . Strong working knowledge and understanding of ICHGCP, Swiss and other international laws and regulations governing clinical trials. Strong medical/ clinical knowledge. Excellent clinical trial monitoring skills with a high level of attention to detail and sound problemsolving skills. Excellent interpersonal communication skills (verbal and written) . Ability to prioritise multiple tasks and achieve project timelines. Computer skills (MS Office) and experience in e CRF systems, CTMS systems, as [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Associate Director, Biostatistics
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] motivated, proactive, and strategic statistician with strong expertise in EU HTA methodologies to join the SGPAR team and provide statistical solutions to meet EU HTA requirements, including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the EU Joint Clinical Assessment (JCA) . Essential Functions of the job Close collaboration with crossfunctional teams to support the quantitative needs for HTA submissions in Europe Provide strategic statistical input into evidence generation activities and analyses required for the EU JCA Provide quantitative support for local HTA adaptations Influence and shape new ways [. .. ] multiple crossfunctional team members. Knowledge of clinical trial design concepts; indepth knowledge of all phases of the drug development process. Demonstrated skills in the planning, analysis and reporting of clinical trials. Travel Yes, depends on needs. Salary Range Switzerland: 164, 100.00 CHF-205, 100.00 CHF UK: 77, 400.00 GBP-96, 700.00 GBP Be One does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Bubenheim, Rheinland- Pfalz
Job Overview We are seeking a
Clinical Research
Associate (m/w/d) to join our team at our innovative research facility in Schwabenheim (near Mainz) . This is a full-time [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] position on a two-year fixed-term contract. Main Responsibilities Conducting paper and electronic clinical studies under the direction of the Clinical Study Team Leader Supporting the planning/ [. .. ] they are equally qualified. Required Skills Adverse Event Report, Clinical Evaluation Reports, Clinical IT, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Good Clinical Data Management Practice (GCDMP) , Good Clinical Practice (GCP) , Investigations Training, Patient Recruitment, Quality Mindset, Regulatory Training #J-18808-Ljbffr 94760592 [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Associate Director Engineering (m/f/d)
Führungs-/ Leitungspositionen
[. .. ] develop breakthrough treatments and find new ways to bring cures to as many people as possible. This is where you come in; the Device Technology Solution Center [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] needs you as Associate Director Engineering for the development of drug device combination products, working alongside our talented, bright and diverse teams. Our Device Technology Solution Center drives the technical development of auto-injectors as well as novel drug delivery principles, e. g. drug delivery to the brain or radioligand therapy. We closely collaborate [. .. ] Create and maintain relevant Design History File (DHF) documents, ensuring high-quality device design and development. Contribute to all phases of medical device development. Ensure components meet quality standards for clinical trials and commercial production. Collaborate with internal and external partners. Identify root causes of issues, define and implement robust solutions. Essential Requirements Degree in mechanical engineering or equivalent. Preferably 10+ years of experience in medical device development. Proficient spoken communication and excellent technical writing skills in English; preferably also German. Proven [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• 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 Progressive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 13 Tagen bei Jobleads gefunden
Associate Director, Project Management, Tech Ops
• Bern
Führungs-/ Leitungspositionen
Position Description Summary Researches and develops new medicines for unmet medical needs through innovative medical science from inception, through
clinical trials to commercialization. Assesses, monitors and ensures products meet clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety standards. Conducts sophisticated analysis, manages research information systems and technical documentation. May be involved in providing para-professional laboratory support for product testing after collection. Establishes relationship with regulatory authorities to establish and maintain registration licenses to sell products globally. [. .. ]
Job am 07.06.2026 bei Jobleads gefunden
Clinical Research Associate (m/w/d)
• Schwabenheim an der Selz, Rheinland- Pfalz
Position
Clinical Research
Associate (m/w/d) fulltime, twoyear fixedterm contract, at our research facility in Schwabenheim (near Mainz) . Responsibilities Conduct paper and electronic clinical studies under the direction [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of the Clinical Study Team Leader. Support planning, organization, and archiving of clinical studies (field and laboratory) . Label investigational products according to Good [. .. ] ideally another European language. Required Skills Adverse Event Report Clinical Evaluation Reports Clinical IT Clinical Research Methods Clinical Site Management Clinical Study Management Clinical Trial Management Clinical Trial Planning Clinical Trials Monitoring Good Clinical Data Management Practice (GCDMP) Good Clinical Practice (GCP) Investigations Training Patient Recruitment Quality Mindset Regulatory Training EEO Statement We are an equal opportunity employer, committed to fostering an inclusive and appreciative workplace. People with severe disabilities and their equivalents will be given preference if they are equally [. .. ]
Job am 07.06.2026 bei Jobleads gefunden
Clinical Research Associate (m/f/d)
• Wien
[. .. ] and products and services in our Allergan Aesthetics portfolio. Job Description You are an excellent organizer and have outstanding social skills and persuasive ability? Then this key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role as a Clinical Research Associate is exactly right for you As a research-based biopharmaceutical company, Abb Vie is one of the most successful companies in the industry internationally and a top employer in Austria. We are currently looking for active support for the Clinical Research Team at our Vienna location. Motivated and experienced CRAs [. .. ] your interests in a fulfilling career and actively change patients lives for the better Your responsibilities Supporting and maintaining continuous communication with study sites in the implementation of global clinical trials. Site management and monitoring activities, such as on-site and remote site initiations, monitoring and close-out visits for clinical trials in Phases IIV, independent management of sites, and training of study physicians and site staff before site activation, as well as during the study. Preparing and updating study-related [. .. ]
Job am 07.06.2026 bei Jobleads gefunden
Associate Director, Biostatistics
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
Associate Director, Biostatistics The Associate Director (AD) , Biostatistics leads the full scope of statistical contribution to a
clinical development program. The AD provides statistical strategies for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. Responsibilities Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence [. .. ]
Job am 07.06.2026 bei Jobleads gefunden
Clinical Research Associate: Site Monitoring, Vienna
• Wien
Power To Fly is seeking a motivated
Clinical Research
Associate in Vienna. The successful candidate will support clinical
trials, manage study sites, and ensure compliance with regulations. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] A degree in natural sciences or relevant experience is required, along with strong organizational skills and proficiency in English and German. This role offers the opportunity to travel and work within a diverse team dedicated to improving patients lives. #J-18808-[. .. ]
Job am 06.06.2026 bei Jobleads gefunden
Commercial Lead Clinical Trial Supply Strategic Accounts (m/f/d)
• München, Bayern
Führungs-/ Leitungspositionen
Commercial Lead
Clinical Trial Supply Strategic Accounts (m/f/d) About the Role Are you a commercially driven professional with a passion for strategic customer relationships and business growth? Were seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a dynamic individual to lead and expand our Special Customer business across Europe. This role is ideal for someone with strong commercial [. .. ] Drive the expansion of our Special Customer business into a dedicated European Business Unit Manage and grow relationships with key national and international customers, focusing on comparator sourcing for clinical trials Develop tailored solutions and partnership models, including contract negotiation and strategic account planning Collaborate with internal teams (Supply Chain, Customer Service, Quality) to ensure smooth delivery and customer satisfaction Prepare forecasts, performance reports, and executive-level presentations to support decision-making Identify market opportunities and support portfolio development through customer [. .. ] scope with minimal travel A collaborative, openminded company culture with room for personal development Apply now and bring your commercial expertise to a growing European business. Position Details Seniority level: Associate Employment type: Full-time Job function: Sales, Business Development, and Customer Service Industries: Pharmaceutical Manufacturing, Wholesale, and Biotechnology Research #J-18808-Ljbffr 94270739 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Associate pro Jahr?
Als Clinical Trials Associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 80 offene Stellenanzeigen für Clinical Trials Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Associate Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Clinical Trials Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Associate Stellenangebote:
- ICON (6 Jobs)
- IQVIA Argentina (2 Jobs)
- IQVIA (2 Jobs)
- TFS Health Science (2 Jobs)
- Parexel (2 Jobs)
- Indero (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Associate Jobs werden derzeit in Sachsen-Anhalt (9 Jobs), Rheinland-Pfalz (9 Jobs) und Bayern (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Associate Jobs?
Clinical Trials Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
