182 Jobs für Clinical Quality Associate
Stellenangebote Clinical Quality Associate Jobs
Job am 11.07.2025 bei Jobleads gefunden
• Baden- Württemberg
Führungs-/ Leitungspositionen
Associate Director-(Senior) Patient Safety Physician (gn) : Oncology Baden-Württemberg, Germany, or relocation to Germany (relocation assistance available) . #clientvacancy #director #pv oncology Together with a German member of INRALS (International [...]
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[...] Network of Recruitment Agencies in Life Sciences) , we are looking for an Associate Director Patient [. .. ] the global initiatives for Patient Safety and Pharmacovigilance (PSPV) and Risk Management (RM) pertaining to compounds at various stages of development. In this role, you will work closely with the clinical development department and will be involved in a very strategic and global function. TASKS RESPONSIBILITIES: Crafting proactive, patient-centric RM strategies tailored to designated compounds. Overseeing and executing all PV activities pertinent to assigned drugs, encompassing database setup, continual safety monitoring, and addressing safety concerns. Engaging in cross-functional collaboration [. .. ] involvement in regulatory submissions would be advantageous. Clinical or research experience in oncology are a big plus. Strong interpersonal and communication skills. Strong ethical sense coupled with a focus on quality and patient safety. Excellent English language skills, both written and verbal. BENEFITS: Highly strategic and development-related role. High-impact on the development of new drugs. Global and intercultural work environment. #J-18808-Ljbffr 55042181 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
P C Business Partner
• Basel, Basel- Stadt
[. .. ] of millions. We maximize impact for patients with cancer by translating biological insights into meaningful therapies. Pharmaceutical Sciences (PS) provides the evidence that a molecule is safe [...]
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[...] and efficacious in clinical proof of concept studies and can be filed as a new medicine. The position leads and drives change initiatives, people streams, Work Product Teams (WPTs) , and squads to embed and execute P C strategies effectively. Additionally, it may contribute to WPTs, squads, or initiatives in other areas of the [. .. ] and reward and recognition in partnership with RDS Business Partner Enterprise, other RDS P C Business Partners/ Business Partners Advisory, other P C Chapters and subjectmatter experts to develop high quality solutions Maintaining broadbased knowledge of multiple leadership areas across the organisation and its operations; uses knowledge of business and P C insights, metrics, expertise, and decision principles to effectively diagnose topics with a wide range of complexity Recommending business practice/ work process improvements to identify opportunities for leveraging human capital; [. .. ] explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver lifechanging healthcare solutions that make a global impact. Lets build a healthier future, together. Seniority level Associate Employment type Fulltime Job function Human Resources Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing Roche is an Equal Opportunity Employer. Get notified about new Business Partner jobs in Basel, Basel, Switzerland. #J-18808-Ljbffr 73212083 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Absolventen, Einsteiger, Trainees
The
Clinical Research
Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or [...]
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[...] health/ life science interest and background who want to explore the research field, travel throughout Germany, Austria, Switzerland, and be part of a [. .. ] paths with opportunities for professional growth Companysponsored employee appreciation events Employee health and wellness initiatives Awards Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr 73212361 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical AI Consultant (f/m/x)
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Join to apply for the
Clinical AI Consultant (f/m/x) role at Helmholtz Munich Shape the future of clinical AI and join us as a Clinical AI Consultant (f/m/x) at Helmholtz [...]
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[...] Munich. Our goal is to empower clinicians and medical researchers to harness AI for real-world impact. Since its inception in 2020, [. .. ] tools in the clinics. Responsibilities Conceptualize, develop and maintain machine learning models to solve concrete clinical questions, in close collaboration with clinical partners and the Helmholtz AI consultant team Develop quality software to bring those models into proofofconcept tools and deploy them in the clinics Be a point of contact for questions related to ML/ AI and medical applications Provide critical assessments of the projects of our clinical partners Continuously learn about stateoftheart and emerging AI methods for clinical applications Profile [. .. ] gender, cultural background, nationality, ethnicity, sexual identity, physical abilities, religion or age. Qualified applicants with physical disabilities will be given preference. Learn more about diversity at Helmholtz Munich Seniority level Associate Employment type Full-time Job function Health Care Provider, Research, and Engineering Industries Research Services #J-18808-Ljbffr 73209180 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Köln, Nordrhein- Westfalen Koeln
Work-Life-Balance
CRA II Senior/ Lead
Clinical Research
Associate (CRA) Remote, Germany Are you an experienced CRA looking for your next significant career step within the German clinical landscape? Do you thrive [...]
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[...] in an environment that values a thoughtful approach to site management and prioritises employee well-being? If so, we have a great opportunity for you to join [. .. ] will play a crucial role in ensuring the smooth and efficient conduct of clinical trials, working with a network of sites across Germany. What sets this team apart? Focus on Quality, Not Just Metrics : They champion a solid thought process in site management, understanding that effective collaboration and proactive problem-solving are paramount. The team empowers their CRAs to manage their sites effectively without the burden of a rigid minimum days on site quota. Genuine Career Development : The organisation [. .. ]
Job gestern bei Jobleads gefunden
Site Relationship Manager
• Essen, Nordrhein- Westfalen
About this role 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 [...]
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[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by understanding the local environment, creating and maintaining strong, longterm relationships with sites, and supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a freelance opportunity at [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Job gestern bei Jobleads gefunden
• Wien
Freiberuflich
Get AI-powered advice on this job and more exclusive features. Direct message the job poster from EPM Scientific Vice President-Recruiting in the
Clinical Operations, Clinical Development and Medical Affairs [...]
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[...] space across Europe EPM Scientific is currently partnered with a CRO client running a project in Austria. They are urgently seeking an experienced Freelance CRA to support their expanding clinical operations team. Contract Conditions Start date: ASAP/ January Location: Remote, Austria Contract Type: Freelance/ [. .. ] and site staff. Review source documents and verify CRF data accuracy. Track study progress and ensure timely resolution of queries. Collaborate with project managers and clinical teams to ensure high-quality deliverables. Previous experience in Dermatology and/or Rare Paediatric Disease studies highly desirable. Strong knowledge of ICH-GCP and Austrian regulatory requirements. Excellent organizational skills and ability to work independently in a remote setting. Fluency in German and English. If this role is of interest to you, please apply directly [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Associate
Clinical Research
Associate page is loaded # # Clinical Research Associatelocations: Germany Remotetime type: Full timeposted on: Posted 14 Days Agojob requisition id: R31245Be One continues to grow [...]
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[...] at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly [. .. ] activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/ hematology clinical trials within the assigned region. The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained. Identify gaps and areas for improvement and propose CAPA. Supports [. .. ]
Job gestern bei Jobleads gefunden
• Wien
[. .. ] in a single step for humans and animals alike. Allergies are diagnosed in a highly specific manner so that patients receive help by their specialist in no [...]
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[...] time. We increase quality of life, enable personalized treatment, advance research and relieve our health system. Location: Vienna, Austria Benefits Annual pass for Viennas public transport and Sodexo vouchers Collaboration with people who care about human and veterinary patients alike An environment where you feel empowered to ask questions, make requests and offer ideas [. .. ] data mining techniques to clean and prepare data sets of varying sizes Refactor and document data processing functions Maintain the existing data dashboards and tools Statistical analysis of data from clinical studies (incl. complex modelling) for publications, presentations at conferences and product development Qualifications Completed education in the field of data science, biostatistics or equivalent Python, R Studio skills or equivalent Excellent command of English; German language skills are advantageous but not necessary Motivation to grow in exciting projects within a [. .. ] offer a payment in line with the collective agreement (KV Handwerk und Gewerbe) based on a parttime position. Your actual salary depends on your previous experience and qualifications. Seniority level Associate Employment type Fulltime Job function Information Technology, Science, and Engineering Industries Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing Ready to become part of the MADx team? Then apply with your CV at our website #J-18808-Ljbffr 73146794 [. .. ]
Job gestern bei Jobleads gefunden
Associate Sales Representative-Imaging
• München, Bayern
[. .. ] opening up of new business fields and expansion of our product range help to secure continuous growth and enable us to take a leading role in the [...]
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[...] development of high-quality products both today and in the future. A major factor in this success is the commitment of our employees, in return for which we offer a motivating work environment where staff are valued and treated with respect. Arthrex is a fast-growing Medical Device company in the Healthcare sector, specialising [. .. ] Managing expectations of all cases to ensure priority cases are covered. Education and professional experience: Ideally degree educated. Relevant fields like medical, anatomy, sciences, physiotherapyor technology beneficial. Experience in a clinical/ theatre role, ideally focusing onendoscopic equipment, surgicalendoscopyor medical sales. Ability to manage relationships with professionals and theatre staff. General requirements: Good organisation, time managementskillsand ability to prioritise workload. Proactive, self-motivatedand disciplined individual with ability to learn quickly andretainproduct knowledge. High levelof competency and understanding of human anatomy Practical and [. .. ]
Job gestern bei Jobleads gefunden
• Penzberg, Bayern
[. .. ] and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Behind every Roche [...]
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[...] product, whether in clinical trials or on the market, stands Pharma Global Technical Operations, a global organization with over 10, 000 employees committed to delivering safe and high-quality medicines. Pharma Technical Development, a key part of this effort, is dedicated to developing innovative solutions for new therapies to meet patient needs. Within Pharma Technical Development, Synthetic Molecules Technical Development (PTDC) focuses on the technical development of our synthetic molecule pipeline and ensures the manufacture of clinical supplies for [. .. ]
Job gestern bei Jobleads gefunden
Medical Science Liaison Hematology
• Köln, Nordrhein- Westfalen Koeln
[. .. ] This person will proactively manage medical scientific stakeholders and create value for patients through medical and scientific stakeholder engagement, medical scientific projects and scientific communications. This role [...]
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[...] reports to the Associate Director Medical Science Liaison. Key responsibilities: Identify, develop and maintain collaborative relationships with KOLs, scientific experts and other medical scientific stakeholders. Compile, analyze, prepare and deliver high quality medical pharmaceutical and scientific communications in line with defined communication plans. Create and execute stakeholder engagement plans, according to Sobis high standards. Support country Global Brand team in developing local medical tactics and provide input to Headquarter (HQ) / regional plans if relevant. Organize and set up scientific advisory boards [. .. ] Qualifications Education/ Learning Experience/ Work Experience Required: University degree in medical/ science or other relevant field +3 years of direct experience in the medical environment Experience from medical affairs, medical/ clinical science, clinical development, access and health economy Experience in hematology, oncology, immune thrombocytopenia, lymphoma In-depth knowledge of national healthcare systems and practices Experience in KOL Management and Account Planning Ability to create and network with KOLs at national level Experience working with KOLs within hematology, oncology, immune thrombocytopenia, lymphoma [. .. ]
Job gestern bei Jobleads gefunden
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] Tok. Stellenbeschreibung More than a job. Its a chance to make a real difference. At Abb Vie, we strive to push the boundaries of science and innovation [...]
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[...] to improve life quality globally. As part of our vibrant team, youll help transform the possibilities in neurological and psychiatric care into realities. Join a global powerhouse with over 50, 000 employees worldwide, including 3, 000 in Germany, where your expertise will address tomorrows unmet medical needs. As an Associate Director/ Director CMC Product Development [. .. ] product. You serve as the spokesperson for all CMC functions and ensures information flow among AST and various line functions and stakeholders. You will also partner with key collaborators, incl. Clinical, Regulatory, Operations, Quality, Preclinical Safety, ADME and Commercial organizations. Apprises CMC and Stakeholder Management of strategies, plans and risks through regular communications and periodic reviews throughout development and in support of global filings and approvals. In addition you support and implement CMC functional initiatives and across-asset strategies. Make your [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Site Relationship Manager
• Hamburg
[. .. ] Relationship Manager role at TFS Health Science. 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 entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. About This Role The Site Relationship Manager (SRM) covers multiple indications within the assigned country throughout the full life cycle of the trial. The key focus areas are to facilitate optimal clinical trial setup, execution, and quality by: understanding the local environment, creating and maintaining strong, longterm relationships with sites, supporting applicable Sponsor Teams in CRO and Sponsor site oversight activities. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a freelance opportunity at around [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Köln, Nordrhein- Westfalen Koeln
Führungs-/ Leitungspositionen
Alimentiv Cologne, North Rhine-Westphalia, Germany
Clinical Operations Lead Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical [...]
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[...] Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation [. .. ] departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities Assist in vendor management activities as required per project Perform review of visit reports for quality, compliance and appropriate site management Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc. ) and inform clinical project team on progress Contribute to financial project [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Operations Lead
• München, Bayern
Führungs-/ Leitungspositionen
This range is provided by Alimentiv. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range Responsible for the [...]
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[...] clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation [. .. ] departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities Assist in vendor management activities as required per project Perform review of visit reports for quality, compliance and appropriate site management Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review, etc. ) and inform clinical project team on progress Contribute to financial project [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Berlin
Were Hiring: RN
Clinical Nurse at Theda Care Juliette Manor The RN Clinical Nurse plays a key role in delivering patient-centered, specialized, evidence-based nursing care across the continuum through [...]
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[...] an interprofessional approach to treatment, research, education, and advocacy. This role supports our mission by ensuring compassionate, safe care within the scope of practice defined by the Wisconsin Board of Nursing and Theda Care policy. Through collaboration with the care team, youll help drive patient outcomes that reflect the high-quality care Theda Care is known forwhile also contributing to a culture of innovation, growth, and professional development. Flexible Scheduling 8 or 12-hour shifts Part-Time and Full-Time Opportunities Insights from Nursing Supervisor Utilize the nursing process, evidence-based practice, and competencies to assess patient needs and develop collaborative [. .. ] materials, or aggressive patients If youre passionate about high-quality patient care and want to grow within a supportive, innovative environmentthis could be the right fit for you. Seniority Level Associate Employment Type Full-time Job Function Other Hospitals and Health Care #J-18808-Ljbffr 72998013 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Führungs-/ Leitungspositionen
Clinical Operations Lead Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research
Associate (CRAs) and [...]
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[...] Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation [. .. ] departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities Assist in vendor management activities as required per project Perform review of visit reports for quality, compliance and appropriate site management Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review, etc. ) and inform clinical project team on progress Contribute to financial project [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] with crossfunctional project teams and external business partners to develop CMC regulatory strategies and identify regulatory risks, representing the department in crossfunctional project teams. Identify required documentation [...]
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[...] and any content quality and timeline issues for global submissions and manage the delivery of approved technical documents in accordance with project timelines. Manage the preparation, authoring, and maintenance of regulatory submission documents pertaining to CMC data for global clinical trial and marketing applications as well as postmarketing variations. May require technical regulatory authoring of submission package components. Support the evaluation of manufacturing changes for potential impact on products. Provide expert review of CMC documentation supporting regulatory submissions and communications. Coordinate preparation of responses to queries from regulatory authorities, particularly [. .. ] and/or interns. Develop and implement regulatory operating guidelines and common work practices/ strategies within the team. Qualifications 1012 years of related work experience (Director candidates typically bring 12 years; Associate level candidates may be considered with 10 years and strong potential) , including 8 years in Regulatory Affairs CMC in the biotech/ pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus. Proven experience serving as a primary RACMC contact to health [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Site Management Associate
• Wien
We are the company that cares for our staff, for our clients, for our partners and for the
quality of the work we do. A dynamic, global company founded [...]
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[...] in 1995, we bring together 3, 000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents information. The scope of responsibilities will include: Maintenance of databases and tracking systems Work with largeamount of documents, including their compiling, procurement, processing, translation and filing Communication with company departments and external parties Communication point for investigative sites participating in the [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Research Associate (CRA) (m/w/d) Zelltherapie (Außendienst)
• Hamburg
Clinical Research
Associate (CRA) (m/w/d) Join to apply for the Clinical Research Associate (CRA) (m/w/d) role at Astra Zeneca Innovativ, dynamisch und nachhaltig: Als eines der weltweit führenden [...]
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[...] Unternehmen der forschenden Arzneimittelindustrie bieten wir bei Astra Zeneca die besten Möglichkeiten für Ihre persönliche und berufliche Entwicklung. Denn für uns [. .. ] zum lokalen Studienteam Stärken beweisen Abgeschlossenes naturwissenschaftliches/ medizinisches Studium Vorerfahrung als Monitor:in in der Durchführung klinischer Studien im Bereich Zelltherapie Interesse an modernen Monitoring Arbeitsweisen wie z. B. Risk Based Quality Management und Remote Monitoring und die uneingeschränkte Bereitschaft, sich diese anzueignen und umzusetzen Hervorragende ICHGCP Kenntnisse zur ordnungsgemäßen Durchführung klinischer Studien Kenntnis der entsprechenden Gesetze (AMG) und regulatorischen Anforderungen Gutes Verständnis hinsichtlich medizinischer Fragestellungen Verständnis von unterschiedlichen Studien und Prozessanforderungen und daraus abgeleitetes Setzen der richtigen Prioritäten Erfahrung im Monitoring [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Site Relationship Manager
• Kassel, Hessen
Site Relationship Manager 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 [...]
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[...] expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. This is a freelance opportunity at around 0.7 FTE. The role focuses on facilitating optimal clinical trial setup, execution and quality by understanding the local environment and building strong site relationships. Key Responsibilities Understanding the Local Environment Gain knowledge of the assigned region (treatment standards, healthcare system, regulatory environment, KOLs, site capabilities, etc. ) . Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Director Project Delivery
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 [...]
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[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Director Project Delivery-home based in Poland, Portugal, Italy, Sweden or UK. About this role We are seeking an experienced and dedicated Line Manager to lead our Trial Master File (TMF) and Clinical Research Associate (CRA) functional teams within the dynamic Ophthalmology Business Unit. This critical role involves strategic oversight, team leadership and operational management to ensure the efficient execution of clinical trials and the maintenance of regulatory compliance. Key Responsibilities Team Leadership Line Management Provide strong leadership, mentorship, and line management to a team [. .. ] based Key Performance Indicators (KPIs) for both the TMF and CRA teams. Utilize KPI data to identify trends, drive process improvements, and ensure functional teams are meeting performance targets and quality standards. TMF Strategy Budgeting Hold responsibility for supporting TMF-related activities during the pre-award budget planning phase, including resource estimation and proposal input. Contribute to the operational strategy for TMF management, ensuring inspection readiness, data integrity, and compliance with all applicable regulations (GCP, ICH guidelines, etc. ) . Drive [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Research Fellow-Dermatology, Randwick Clinical Campus
• Berlin
Senior Research Fellow Dermatology, Randwick
Clinical Campus (UNSW) Employment Type: Full Time, 35 hours per week Duration: 12 months fixed term Remuneration: 150 K-172 K (based on experience) + [...]
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[...] 17 superannuation + leave loading Location: Randwick, New South Wales Why This Role Matters The Senior Research Fellow role involves conducting independent, high-impact research, building [. .. ] of immunotherapy. Strong leadership, collaboration, and organisational skills are essential, along with a commitment to professional development, ethical conduct, and workplace health and safety. The position will report to the Associate Professor and has no direct reports. Skills Required A Ph D in epidemiology, and/or relevant work experience with medical qualification and specialist qualification in dermatology (FACD or international equivalent) Experience in management of cutaneous toxicities of immunotherapy. Proven commitment to proactively keeping up to date with discipline knowledge and developments. Demonstrated track record in research with outcomes of high quality and high impact with clear evidence of the desire and ability to continually achieve research excellence as well as the capacity for research leadership. Demonstrated ability to work in a team, collaborate across disciplines and build effective relationships. Evidence of highly developed interpersonal and organisational skills. An understanding of and [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Associate Director, Study Start-Up
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] seeking a key manager to support the Medpace Study Start-up group in Europe while being office-based in Munich. This position will be an integral part of the [...]
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[...] Medpace clinical operations management team. This role will be responsible for the strategic development of the group, management of the team, and continuous improvement of processes. As a leader of the Study Start-up team, you will be responsible for providing input on new business development opportunities and developing and maintaining relationships [. .. ] by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023, and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/ AA Employer m/f/Disability/ Vets #J-18808-Ljbffr 72809059 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical quality associate pro Jahr?
Als Clinical quality associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Quality Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 182 offene Stellenanzeigen für Clinical Quality Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Quality Associate Jobs?
Aktuell suchen 11 Unternehmen nach Bewerbern für Clinical Quality Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Quality Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Quality Associate Stellenangebote:
- Astra Zeneca (19 Jobs)
- CCS- Global (11 Jobs)
- Veeda Lifesciences (11 Jobs)
- TFS Health Science (10 Jobs)
- ICON (6 Jobs)
- IQVIA (5 Jobs)
In welchen Bundesländern werden die meisten Clinical Quality Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Quality Associate Jobs werden derzeit in Nordrhein-Westfalen (20 Jobs), Bayern (19 Jobs) und Berlin (16 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Quality Associate Jobs?
Clinical Quality Associate Jobs gehören zum Berufsfeld Qualitätswesen.
