40 Jobs für Clinical Research Coordinator
Stellenangebote Clinical Research Coordinator Jobs
Job am 02.09.2026 bei JobMESH gefunden
Carl von Ossietzky Universität Oldenburg
• Niedersachsen 26129 Oldenburg
Abgeschlossenes Studium Abgeschlossene Ausbildung
Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] im wissenschaftlichen Arbeiten und/oder Projektmanagement Erfahrungen im Umgang mit Forschungsdatenbanken oder Studienregistern Weiterbildungen: Good-Clinical-Practice-(GCP) - Zertifikat, Kurs zur Studienkoordination, Weiterbildung Clinical Research Associate (CRA) , Weiterbildung
Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Research Coordinator (CRC) , Projektmanagement (z. B. PRINCE2, PMP, Scrum) , Drittmittelmanagement, Forschungsdatenmanagement, Medizinische Statistik, Datenschutz im Gesundheitswesen, Forschungsrecht und Ethik Wir bieten Strukturierte Einarbeitung, intensive Betreuung und eine kollegiale Arbeitsatmosphäre, die die fachliche und persönliche Weiterentwicklung unterstützt Mitarbeit in innovativen, interdisziplinären Forschungsprojekten im Bereich der klinischen Kinderpsychologie und -psychiatrie Möglichkeit, eigene [. .. ]
▶ Zur Stellenanzeige
Job vor 4 Tagen bei Jobleads gefunden
Entry-level Clinical Research Associate-Clinical Study Coordinator experience
Clinical Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of
Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ]
▶ Zur Stellenanzeige
Job am 03.09.2026 bei Jobleads gefunden
[. .. ] the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Qualifications Must have a minimum of a Bachelors degree in a health or science related field; [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Experience as a Clinical Research Coordinator (minimum 1 year) ; Ability to travel 60-70 to locations in the DACH region; Proficient knowledge of Microsoft Office; Must be detail-oriented and efficient in time management Excellent verbal and written communication and presentation skills in German and English. We kindly ask to submit your application in English. [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Clinical Research Nurse
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
• Berlin
[. .. ] Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Neu Job vor 2 Std. bei StepStone gefunden
Astra Zeneca
Senior Manager (m/f/d) Cell Therapy Hub
• bundesweit
[. .. ] are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. This role is part of the Oncology R D team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] tasked with supporting Clinical and Commercial production across multiple sites. Aufgaben We are looking for a Senior Manager (m/f/d) Cell Therapy Hub (field-based) The Senior Manager (m/f/d) , Cell Therapy Hub is primarily responsible for managing each patient and cell journey throughout the treatment. This dynamic role requires an [. .. ] and comply with applicable SOPs and regulations. Profil Experience Skills: BA or BS degree or equivalent experience. Minimum of 4 years of experience within a Cell Therapy Program as a: Research Coordinator, Nurse Coordinator, Apheresis Nurse, Cell Lab Professional, Quality Manager, in the healthcare systems or regulatory environment. Solve site facing problems and deal with organizational complexity. Desirable Skills : Advanced degree in Life Sciences or Engineering (e. g. , Pharm D, NP, PA, Biomedical Engineer) Experience working with critical raw material suppliers [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
• Leipzig, SN
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Frankfurt
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Berlin, BE
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Dortmund, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Munich, BY
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Cologne, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Hamburg, HH
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Düsseldorf, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Essen, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates should have [. .. ]
Job gestern bei Mindmatch.ai gefunden
Triwill Group
Senior Project Coordinator
• AT- 2 Lavamünd
Description: This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Project
Coordinator based in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Switzerland. As a Senior Project Coordinator, you will play a key role in supporting site activation and site-level deliverables throughout the clinical trial lifecycle. You will collaborate closely with Project Managers, Clinical Trial Managers, Site Selection teams, CRAs, clinical sites, and other stakeholders. The role combines project coordination, regulatory documentation, communication, and operational oversight in a global, multi-regional environment. You will take ownership of timelines, quality, and priorities to help ensure [. .. ] senior team member, you will work autonomously while also supporting and mentoring junior colleagues when needed. This is an opportunity to make a tangible impact in a fast-growing clinical research environment while contributing to the successful delivery of clinical trials. J-18808-Ljbffr 03498667 [. .. ]
Job gestern bei Mindmatch.ai gefunden
Triwill Group
• AT- 2 Lavamünd
Triwill Group, on behalf of a partner company, is seeking a Senior Project
Coordinator based in Switzerland to support site activation and site-level deliverables across the
clinical trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lifecycle. You will collaborate closely with Project Managers, Clinical Trial Managers, Site Selection teams, CRAs, and clinical sites to ensure timelines and quality are maintained. You will work autonomously while mentoring junior colleagues, contributing to a fast-growing clinical research environment and J-18808-Ljbffr 03500282 [. .. ]
Job gestern bei Jobleads gefunden
(Senior) Clinical Project Coordinator (f/m/d)
• Karlsruhe, Baden- Württemberg
[. .. ] of our billions of Med Tech products per yearto look at the impossible and find transformative solutions that turn dreams into possibilities. Responsibilities Job Description Provide operational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support for BDPI clinical studies to enable successful completion of study objectives and deliverables. Prepare and ship clinical study supplies (e. g. , study binders, mini protocols, etc. ) and investigational products from BD Peripheral Interventions headquarters to domestic and international locations for assigned clinical studies. Serve as a Clinical Product Management expert and [. .. ] Quality Management System (QMS) Required Skills Competencies Bachelors Degree (BS/ BA) in life sciences or equivalent combination of training and experience (MA/ MS preferred) 1+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology) , with supply inventory management/ shipment, or in a clinical setting Proficiency with Microsoft Suite tools (Outlook, Word, Excel, Power Point, One Note, To-Do, Share Point, etc. ) Strong interpersonal and communication/ presentation (oral and written) skills Strong organizational skills, attention to detail, [. .. ]
Job gestern bei Jobleads gefunden
Führungs-/ Leitungspositionen
Work-Life-Balance
Team Leader (Player/ Manager)
Clinical Development Liaison (CDL) Neuromuscular Diseases Business Unit: Field Operations Reports to: Program Director, Medical, Amplity Location: Germany Territory: Germany and some other countries in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Europe Role Type: Individual Contributor with Leadership Responsibilities (Player-Coach) About the Role Amplity is partnering with an innovative global biopharmaceutical company dedicated to advancing transformative [. .. ] regional experts, they will gain insight into treatment patterns and trends that will be shared internally to shape strategy. The role is also the field-based leader and key contributor/ coordinator to the overall remit of the clients Medical Affairs organisation for the Amplity Medical team. This position is responsible for leading and coordinating operational requirements of the Amplity team to support the clients Medical Affairs business. The specific deliverables being managed can vary and is defined in the contract Amplity [. .. ] Neuromuscular Diseases. Experience working within Neurology is strongly preferred. Has medical knowledge and is skilled at scientific discussions. Proven success of relationship building with HCPs/ SCs/ KOLs. Knowledge of clinical research in various the appropriate region including optimization of enrolment strategies. Possess strong verbal and written communication, interpersonal and organizational skills. Able to use initiative and problem solve. Flexible and adaptive approach to work. Ability to identify issues and resolve appropriately with guidance. Ability to function well, both independently and within [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Associate (m/w/d) Region: Stuttgart, Heilbronn, Heidelberg
[. .. ] that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. bms. com/working-with-us. Position Summary The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs) , International Council for Harmonization (ICH) Guideline for Good Clinical Practice [. .. ] years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role Relevant prior Pharma/ Biotech Sponsor employment or experience as a clinical study coordinator preferred Experience in the drug discovery/ development process. Competencies Knowledge and understanding of clinical research processes, regulations and methodology Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management Working knowledge of ICH/ GCP Guidelines and applicable local laws and regulations (that govern clinical [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Clinical Research Associate (Germany)
• Berlin
Junior
Clinical Research Associate (Germany) Role Summary The role supports the organization and execution of clinical studies in Germany. It involves working with internal teams and external partners to ensure [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] that studies run smoothly, in accordance with timelines, quality standards, and applicable regulations. Key Responsibilities Support the coordination and day-to-day follow-[. .. ] and fast-paced environment. Required Qualifications Relevant background in life sciences, healthcare, nursing, engineering, or a related field. A first relevant experience in clinical research (CTA, Study start-up, Study Coordinator, . . . ) Good knowledge of clinical trial processes and GCP principles. Fluency in German and English. Good organizational, communication, and problem-solving skills. Ability to manage priorities and work independently while collaborating with a wider team. Good knowledge of MS Office and experience with relevant clinical systems. Willingness to [. .. ]
Job am 05.09.2026 bei Jobleads gefunden
Medical Affairs Research Coordinator (m/w/d)
• Frankfurt, Hesse
Medical Affairs
Research Coordinator (m/w/d) Verantwortungsbereich: Koordination der von Medical Affairs initiierten und/oder unterstützten Forschungsprojekte (nicht-interventionelle Studien, Register o. ä. ) einschließlich Projekt- und Budget Tracking. Erstellung und Aktualisierung von [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Präsentationen. Verwalten von Beschaffungs-, Buchhaltungs- und Rückstellungsprozessen. Zusammenstellen und Überprüfen von Daten sowie Integration in vorformatierte Berichte. Interaktionen mit Studienzentren und ggf. Besuche in Deutschland. Koordination von Aktivitäten mit dem Coordination Office und anderen internationalen Abteilungen sowie externen Vendoren. Anforderungsprofil: Mindestens 23 Jahre Erfahrung in ähnlicher Position (Clinical Research Associate, Bachelor of Science oder eine vergleichbare Qualifikation) im internationalen Umfeld. Erfahrung im Projektmanagement von Vorteil. Sehr gute organisatorische Fähigkeiten. Strukturierte und gründliche Arbeitsweise. Sehr gute Kommunikationsfähigkeit. Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Sehr gute Computerkenntnisse (MS Office etc) . Erfahrung mit wissenschaftlichen/ medizinischen Studien in [. .. ]
Job am 04.09.2026 bei Jobleads gefunden
Medical Affairs Research Coordinator (m/w/d)
• Frankfurt, Hesse
[. .. ] Interaktionen mit Studienzentren und ggf. Besuche in Deutschland. Koordination von Aktivitäten mit dem Coordination Office und anderen internationalen Abteilungen sowie externen Vendoren. Anforderungsprofil: Mindestens 23 Jahre Erfahrung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in ähnlicher Position (Clinical Research Associate, Bachelor of Science oder eine vergleichbare Qualifikation ) im internationalen Umfeld. Erfahrung im Projektmanagement von Vorteil. Sehr gute organisatorische Fähigkeiten. Strukturierte und gründliche Arbeitsweise. Sehr gute Kommunikationsfähigkeit. Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Sehr gute Computerkenntnisse ( MS Office etc ) . Erfahrung mit wissenschaftlichen/ medizinischen [. .. ]
Job am 31.08.2026 bei Jobleads gefunden
Associate Director, Trial Clinical Delivery Lead (all genders)
• Eysins, Waadt
Führungs-/ Leitungspositionen
Your role Accountable for the delivery and quality of site level activities in Phase I-IV
Clinical Development studies; act as link between Clinical Site Leads (CSLs) , Global functions [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRO counterparts-single point of contact for site management operational topics/ escalations; support information channeling and issue resolution for the study Provide leadership, strategic direction, and operational oversight for Clinical Site Lead (CSL) activities across assigned study [. .. ] medication, etc. Oversee service providers to ensure successful implementation within agreed timelines, budget, and quality. Develop and implement a monitoring strategy in collaboration with Clinical Trial Leads (CTLs) and Contract Research Organizations (CROs) , using a risk-based quality management approach. Continuously update the strategy based on external changes and new internal data. Utilize site performance and quality data analytics to drive proactive, risk-based site oversight practices and quality risk oversight and management across all stages of study delivery. Develop, [. .. ] quality/ costs) and work with CSLs, CTLs, Data Managers, Clinical Lead (s) and other relevant business partners to implement action plans to resolve and/or mitigate. Participate in Investigator/ Study Coordinator Meetings and promote information sharing with the CSLs as needed. Travel: Position may require domestic/ international travel up to 20 of time. Who you are Minimum Requirements: Bachelors Degree Medical or Life Sciences degree in a clinical research related discipline 8-10 years professional and project management experience in delivering [. .. ]
Job am 30.08.2026 bei Jobleads gefunden
Associate Director, Trial Clinical Delivery Lead (all genders)
• Eysins, Waadt
Führungs-/ Leitungspositionen
[. .. ] The position requires to be on-site in Eysins for 3 days per week. Your role Accountable for the delivery and quality of site level activities in Phase [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] I-IV Clinical Development studies; act as link between Clinical Site Leads (CSLs) , Global functions CRO counterparts-single point of contact for site management operational topics/ escalations; support information channeling and issue resolution for the study Provide leadership, strategic direction, and operational oversight for Clinical Site Lead (CSL) activities across assigned study [. .. ] medication, etc. Oversee service providers to ensure successful implementation within agreed timelines, budget, and quality. Develop and implement a monitoring strategy in collaboration with Clinical Trial Leads (CTLs) and Contract Research Organizations (CROs) , using a risk-based quality management approach. Continuously update the strategy based on external changes and new internal data. Utilize site performance and quality data analytics to drive proactive, risk-based site oversight practices and quality risk oversight and management across all stages of study delivery. Develop, [. .. ] quality/ costs) and work with CSLs, CTLs, Data Managers, Clinical Lead (s) and other relevant business partners to implement action plans to resolve and/or mitigate. Participate in Investigator/ Study Coordinator Meetings and promote information sharing with the CSLs as needed. Travel: Position may require domestic/ international travel up to 20 of time. Who You Are Minimum Requirements: Bachelors Degree Medical or Life Sciences degree in a clinical research related discipline 8-10 years professional and project management experience in delivering [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Research Coordinator pro Jahr?
Als Clinical Research Coordinator verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Research Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 40 offene Stellenanzeigen für Clinical Research Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Research Coordinator Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Research Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Research Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Research Coordinator Stellenangebote:
- Triwill Group (2 Jobs)
- Herman Medical Staffing GmbH (2 Jobs)
- Astra Zeneca (1 Job)
In welchen Bundesländern werden die meisten Clinical Research Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Coordinator Jobs werden derzeit in Nordrhein-Westfalen (7 Jobs), Berlin (6 Jobs) und Baden-Württemberg (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Coordinator Jobs?
Clinical Research Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
