145 Jobs für Clinical Data Associate
Stellenangebote Clinical Data Associate Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Homeoffice möglich
Join IQVIA Biotech as a
Clinical Research
Associate 2/ CRA 2 (m/w/d) to work home-based throughout Germany, and preferably in the Munich or Hamburg area. You will enjoy the stability [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and resources of a leading, global contract research organization while gaining direct experience with our clients. This role promises to offer intentional career growth and [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts at study sites and with client representatives. Mentoring less experienced team members, support as subject matter expert for specific topics or additional tasks might be included. Qualifications University Degree in life science or other scientific discipline or apprenticeship in the health care field. Minimum of [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
ICON
Senior CRA
• AT- 9 Wien
Work-Life-Balance
Senior CRA ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
AOP Health
• AT- 9 Wien
Führungs-/ Leitungspositionen
We are looking for an experienced and proactive
Clinical Site Management Lead to oversee the operational management of clinical studies and ensure high standards of quality, compliance, and collaboration with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study sites and partners. What Your Day To Day Will Look Like Manage assigned clinical studies from site start-up through close-out Prepare and coordinate submissions to Competent Authorities and Ethics Committees Conduct co-monitoring visits to ensure patient safety, data integrity, and regulatory compliance Build strong relationships with CRO personnel, site staff, and internal study teams Support and oversee CROs and freelance CRAs Review and analyse clinical study data for accuracy and completeness Ensure availability and quality of essential site documents for the Trial Master File Forecast IMP supply and [. .. ] smooth trial execution Your Qualifications And Experience Bachelors degree or higher in Life Sciences, Pharmacy, Medical Sciences, or a related field Minimum 5 years of experience as a Clinical Research Associate (CRA) or 2 years as a Senior CRA Strong knowledge of clinical trial conduct, regulatory requirements, and ICH-GCP Experience with submissions to Competent Authorities and Ethics Committees Experience with risk-based monitoring Willingness to travel (max. 30-irregular, but can be flexibly divided in the team) Fluent in English [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
ICON
Senior Clinical Research Associate Global Trial Oversight
• AT- 9 Wien
Work-Life-Balance
A leading healthcare organization in Austria is seeking an experienced Senior
Clinical Research
Associate to oversee clinical trial activities and ensure regulatory compliance. The ideal candidate will have an advanced [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] degree in a relevant field and extensive experience in clinical trial processes. You will monitor trial sites, conduct site visits, and collaborate with teams to ensure data integrity and participant safety. ICON offers a competitive salary and comprehensive benefits to support work-life balance. J-18808-Ljbffr 85227186 [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
A
clinical research firm is inviting qualified candidates to join their talent pool for Clinical Research
Associate roles across various seniority levels. Responsibilities include site management,
data review, training support, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and query resolution. Candidates with 13 years of experience in clinical research and an Honours Bachelor Degree are sought after. The company offers a comprehensive benefits package, including base salary and performance bonuses. J-18808-Ljbffr 83945563 [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on our side-[. .. ] Research Associate I/ II Support/ conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance with SOPs, protocol, and GCP. Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
A leading
clinical research organization in Austria is seeking candidates for Clinical Research
Associate positions at various levels. The roles involve supporting site management through monitoring and initiation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] visits while ensuring data quality and compliance. Ideal candidates must hold an Honours Bachelors Degree with relevant experience ranging from 1 to 3 years depending on the level. The organization offers competitive compensation, including a base salary and performance bonuses, along with a comprehensive benefits package. J-18808-Ljbffr 83093352 [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
CRA single sponsor-Germany
• AT- 9 Wien
Description CRA single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. For the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] oversight of the Lead CRA, to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA) . Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Octapharma Austria
• AT- 9 Wien
[. .. ] requests, submissions and inquiries from internal and external stakeholders Manage, coordinate, perform and continuously improve multiple complex lab operations and analytical tasks Critically coach others in laboratory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] excellence, review experimental data and ensure highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
Octapharma Pharmazeutika Produktionsges. m. b. H.
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
• AT- 9 Wien
[. .. ] requests, submissions and inquiries from internal and external stakeholders Manage, coordinate, perform and continuously improve multiple complex lab operations and analytical tasks Critically coach others in laboratory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] excellence, review experimental data and ensure highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
A leading biopharmaceutical solutions organization in Vienna is seeking a
Clinical Research
Associate to oversee clinical trials ensuring compliance and
data integrity. Responsibilities include site qualification, monitoring, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and documentation while providing superior patient support. Ideal candidates possess a degree in a related field, knowledge of clinical guidelines, and fluency in German. This role offers opportunities for personal and professional growth in a dynamic and inclusive work environment. J-18808-Ljbffr 81482935 [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA Germany or Austria-single-client
• AT- 9 Wien
[. .. ] 9, 2025 Location: Vienna, 1, Austria Job ID: 25104265-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor facetoface meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
Updated: Yesterday Location: Vienna, 1, Austria Job ID: 25105750-OTHLOC-3538-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and projectspecific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to [. .. ]
Job am 06.02.2026 bei Mindmatch.ai gefunden
IQVIA LLC
Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austria
• AT- 9 Wien
Homeoffice möglich
Clinical Research
Associate 2 (m/w/d) , IQVIA Biotech, based in Austria page is loaded # # Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austrialocations: Vienna, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1526950External Job Description Join IQVIA Biotech as a Clinical Research Associate 2/ [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts at study sites and with client representatives. Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included. Qualifications: University Degree in life science or other scientific discipline or apprenticeship in the health care field. Minimum [. .. ]
Job am 10.03.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The Study Physician is a critical global role responsible for assuming medical oversight of
clinical trials within Clinical Development Operations. This position requires a qualified and clinically experienced physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] who will provide comprehensive medical expertise throughout all phases of the trialfrom preparation and conduct to reporting. The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to [. .. ] Clinical Trial Protocols (CTPs) . Collaborates with Project Management, Patient Safety, Medical Writers, and trial/ evidence teams. Provides medical input for CTP updates. Risk-Based Quality Management: Defines medically critical data/ processes and associated risks. Contributes to Integrated Quality and Risk Management Plan (IQRMP) . Participates in risk discussions during trial conduct. Clinical Quality Monitoring: Co-authors Clinical Quality Monitoring Plan (CQMP) . Aligns CQMP with IQRMP-identified risks and mitigations. Protocol Deviations Management: Provides medical input on important protocol deviations [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
Associate Medical Director-Oncology, Sponsor-Dedicated (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
The Study Physician is a critical global role responsible for assuming medical oversight of
clinical trials within Clinical Development Operations. This position requires a qualified and clinically experienced physician [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] who will provide comprehensive medical expertise throughout all phases of the trialfrom preparation and conduct to reporting. The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to [. .. ] Clinical Trial Protocols (CTPs) . Collaborates with Project Management, Patient Safety, Medical Writers, and trial/ evidence teams. Provides medical input for CTP updates. Risk-Based Quality Management Defines medically critical data/ processes and associated risks. Contributes to Integrated Quality and Risk Management Plan (IQRMP) . Participates in risk discussions during trial conduct. Clinical Quality Monitoring Co-authors Clinical Quality Monitoring Plan (CQMP) . Aligns CQMP with IQRMP-identified risks and mitigations. Protocol Deviations Management Provides medical input on important protocol deviations [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] ability to drive and deliver multiple projects concurrently. Responsibilities Lead the process development and c GMP manufacture of small molecule drug substances at CDMOs Ensure adequate supply [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of drug substance for clinical studies and other needs. Oversee the development of robust and reliable manufacturing processes utilizing Quality by Design (Qb D) principles. Oversee the synthesis of chemical entities to support clinical and non-clinical studies. Ensure that all DS processes are in line with all applicable regulations, policies, guidelines, and procedures. Represent the [. .. ] budgets desirable. Experience in defending processes, procedures, and investigation during FDA/ EMA (and other competent authorities) inspections desirable. Capability of grasping complex technical issues and make sound decisions based on data and information from various sources. Knowledge of formulation development and/or large molecule technologies would be advantageous. Excellent written and verbal communication skills. Education Bachelors degree and Masters or Ph D in Chemistry #J-18808-Ljbffr 85688666 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Director, Europe Patient Advocacy, Professional Relations, and Patient Engagement
• Zürich Zuerich
Führungs-/ Leitungspositionen
[. .. ] of people with cancer. We are seeking a team-oriented, results-driven professional committed to outstanding collaboration and passionate about strengthening the patient voice in Genmabs decision-making. The Director/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate Director, Patient Engagement Professional Relations (Europe) will lead and advance patient and professional engagement activities across Europe, ensuring the European patient voice is meaningfully represented in Genmabs strategy and decision-making, while partnering closely with global colleagues and alliance partners. Responsibilities European strategy planning Develop and execute a Europe-wide [. .. ] privacy requirements, and Genmab policies. Bring the European patient voice into Genmab Identify, design, and deliver innovative approaches to incorporate European patient insights into Genmab decision-makingespecially with Medical Affairs, Clinical Development, Regulatory, Market Access/ HEOR, Marketing/ Commercial, and Alliance colleagues. Translate patient insights into actionable recommendations and ensure feedback loops back to participating organizations and internal stakeholders. Governance, compliance, and privacy (Europe) Ensure all activities align with applicable European and local requirements and industry codes (e. g. , EFPIA and [. .. ] of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmabs vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines. Established [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austria
• Wien
Homeoffice möglich
Join IQVIA Biotech as a
Clinical Research
Associate 2/ CRA 2 (m/w/d) to work home-based throughout Germany, and preferably in the Munich or Hamburg area. You will enjoy [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the stability and resources of a leading, global contract research organization while gaining direct experience with our clients. This role promises to offer intentional career growth and [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts at study sites and with client representatives. Mentoring less experienced team members, support as subject matter expert for specific topics or additional tasks might be included. Qualifications University Degree in life science or other scientific discipline or apprenticeship in the health care field. Minimum of [. .. ]
Job gestern bei Jobleads gefunden
Associate Director, Biostatistics
• Zürich Zuerich
Führungs-/ Leitungspositionen
The
Associate Director (AD) , Biostatistics, leads the full scope of statistical contribution to a
clinical development program. The AD provides statistical strategies for the clinical trials and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory submissions, and is accountable for the statistical deliverables within the program. 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 and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. Provide [. .. ]
Job gestern bei Jobleads gefunden
Associate Director in Data Science, Digital Health Analytics and Innovation (all genders)
• Darmstadt, Hessen
Führungs-/ Leitungspositionen
[. .. ] and career advancement across the globe. Your Role In this pivotal role, you will build and establish scientific excellence in the development of digital biomarkers and endpoints [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] within the Advanced Data Science team in the Data Sciences organization. You will lead the identification, development, and deployment of novel digital endpoints and outcome measures across clinical trials and life cycle management programs. Collaborating closely with the Global Digital Health organization, you will spearhead the design and validation of machine learningdriven algorithms and data processing pipelines that extract clinically relevant insights from highvolume digital health data sources, such as wearables, sensors and apps, mobile devices, and patientfacing [. .. ]
Job gestern bei Jobleads gefunden
Director, Europe Patient Advocacy, Professional Relations, and Patient Engagement
• Zug
Führungs-/ Leitungspositionen
[. .. ] of people with cancer. We are seeking a team-oriented, results-driven professional committed to outstanding collaboration and passionate about strengthening the patient voice in Genmabs decision-making. The Director/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate Director, Patient Engagement Professional Relations (Europe) will lead and advance patient and professional engagement activities across Europe, ensuring the European patient voice is meaningfully represented in Genmabs strategy and decision-making, while partnering closely with global colleagues and alliance partners. Responsibilities European strategy planning Develop and execute a Europe-wide [. .. ] privacy requirements, and Genmab policies. Bring the European patient voice into Genmab Identify, design, and deliver innovative approaches to incorporate European patient insights into Genmab decision-makingespecially with Medical Affairs, Clinical Development, Regulatory, Market Access/ HEOR, Marketing/ Commercial, and Alliance colleagues. Translate patient insights into actionable recommendations and ensure feedback loops back to participating organizations and internal stakeholders. Governance, compliance, and privacy (Europe) Ensure all activities align with applicable European and local requirements and industry codes (e. g. , EFPIA and [. .. ] the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hardworking, innovative and collaborative team has invented nextgeneration antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific Tcell engagers, antibodydrug conjugates, nextgeneration immune checkpoint modulators and effector functionenhanced antibodies. By 2030, Genmabs vision is to transform the lives of people with cancer and other serious diseases with Knock Your Socks Off (KYSO) antibody medicines. Established in1999, Genmab is headquartered [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Support Associate, Germany (Remote/ Hybrid)
• Berlin
[. .. ] weight management programs combining GLP-1 medication with a tailored nutrition and exercise programme, supported by our multidisciplinary care team of prescribers, health coaches, dietitians, nurses and pharmacists. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Our published clinical research demonstrates that our combined approach to weight management and lifestyle change means that our patients are 4x as likely to lose significant weight through their course of treatment with Juniper. Since launching, weve grown fast to support millions of patients. In 2024 alone In the UK we grew from [. .. ] consent to the use of Metaview for future interviews? Select. . . I confirm that I have read and understood the Candidate Privacy Notice, which explains how Eucalyptus processes personal data for recruitment purposes. Select. . . #J-18808-Ljbffr 85456323 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director, Patient Advocacy, Germany
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] the International/ global Advocacy and Patient Engagement team and beyond, and contribute to global/ international work streams where the local perspective is required Conceptualize and coordinate engagement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of PAOs in clinical development programs running and/or planned in Germany Conceptualize and coordinate engagement of PAOs in the development of local Patient Support Programs (PSPs) working in close partnership with the Patient Medical Program team and local medical team responsible for PSPs Conceptualize and coordinate engagement of PAOs in data generation initiatives (HEOR/ MR) as well as in relation to local HTA processes or other postmarketing and policy initiatives, in close partnership with Medical Affairs and Market Access teams Based on local needs assessment, conceptualize and carry out Patient Advisory Boards, focus groups and roundtables with patient representatives, patients, and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director Operational Excellence (m/f/d)
• Planegg, Bayern
Führungs-/ Leitungspositionen
Associate Director Operational Excellence (m/f/d) Permanent employee, Full-time Planegg (Germany) , Remote (Germany) Be part of our team We are seeking a highly experienced Associate Director of Operational Excellence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (GCP) to lead continuous improvement efforts across our clinical trial operations and ensure adherence to the highest standards of GCP compliance. The position will be within the Quality Assurance (QA) department. We are a dedicated QA team supporting our development of antibody-drug conjugates (ADCs) and clinical trials with a strong focus on reliable processes and patient safety. Working [. .. ] and revise existing documents to reflect optimized, compliant and scalable practices. Facilitate SOP review cycles, incorporating stakeholder feedback and ensuring alignment with internal policies and applicable regulatory requirements. Analyze operational data and performance metrics to drive data-informed decision making and promote accountability. Champion risk-based approaches in clinical operations, including proactive risk identification, mitigation planning, and CAPA oversight. Support inspection readiness activities and serve in close collaboration with QA and the operational teams as a key contributor in internal audits [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical data associate pro Jahr?
Als Clinical data associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 145 offene Stellenanzeigen für Clinical Data Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Associate Jobs?
Aktuell suchen 25 Unternehmen nach Bewerbern für Clinical Data Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Associate Stellenangebote:
- ICON (18 Jobs)
- Astra Zeneca (12 Jobs)
- IQVIA (8 Jobs)
- Alimentiv (3 Jobs)
- Optimapharm d. o. o. (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Data Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Associate Jobs werden derzeit in Hessen (17 Jobs), Sachsen-Anhalt (17 Jobs) und Bayern (17 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Associate Jobs?
Clinical Data Associate Jobs gehören zum Berufsfeld Medizintechnik.
