8 Jobs für Patient Access Coordinator
Stellenangebote Patient Access Coordinator Jobs
Job vor 5 Tagen bei Jobleads gefunden
• Potsdam, Brandenburg
[. .. ] the clinical management of assigned PPM Practice (s) servicing patients in and around SLH in St. Lawrence County, New York. Works collaboratively in dyad relationship with Practice [...]
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[...] Manager (s) / Coordinator (s) in the supervision and support of clinical care coordinators, LPNs and MAs. Collaborate with key function leaders at SLH such as Director of Quality, Director of Patient Safety, and Director of Patient Experience. Responsible for the management of quality clinical standards for employed and contracted physicians, mid-levels (providers) and staff. RESPONSIBILITIES Regulatory and Quality Management Supervises and assures effective, high quality clinical activities within the medical office home. Cooperates with all providers and clinical staff in [. .. ] pharmaceuticals, and instruments. Establishes, implements and monitors all aspects of nursing activities in support of physicians and mid-level providers, nurse practitioners (NPs) , and physician assistants (PAs) . Ensures access to appropriate patient education resources via multiple modalities such as educational handouts, internal support resources, and external patient self-management resources and collaborates with clinical leaders and members of the health care team to make resources available to patients. Example: diabetes, CHF, COPD education, the State of New York Vaccines [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Lausanne, Waadt
Debiopharm, a Swiss biopharmaceutical firm, focuses on Oncology and Infectious diseases. Join us to enhance
patient outcomes and innovate in a supportive environment. Tasks Oversee the entire contract lifecycle and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manage workflows effectively. Act as the Docu Sign expert, providing training and support. Coordinate Joint Steering Committee meetings and track action items. Debiopharm is privatelyowned Swiss biopharmaceutical company committed to research in Oncology and Infectious diseases [. .. ] outcomes and quality of life. Debiopharm International SA aims to develop innovative therapies via our unique development only business model, acting as a bridge between disruptive discovery products and patient access in international markets. At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases through working on innovative medicines for patients. Efficacy is our mode of action, saving lives our collective target. Join our team at Debiopharm where together, we innovate, we impact, and we grow. For our Legal Department based at our Headquarters in Lausanne, Switzerland, we are looking for a Legal Pre Commercial Alliance Coordinator-CDI, 90-100 This central role is dedicated to streamlining administrative workflows and overseeing the full contract lifecycle. You will serve as the departmental hub, providing highlevel support for Confidential Disclosure Agreements (CDAs) and alliancerelated initiatives across the group. Your responsibilities Workflow Oversight: Manage the endtoend contract lifecycle, including formatting [. .. ]
Job am 17.02.2026 bei Jobleads gefunden
• Eysins, Waadt
Führungs-/ Leitungspositionen
[. .. ] clinical trials under your responsibility by driving innovative, value-adding solutions and ensuring the adoption of cuttingedge methodologies. Additionally, you will be responsible for developing and executing effective [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site and patient engagement strategies to secure timely recruitment and retention, ensuring ontime study delivery and successful trial outcomes. As part of our global team, youll collaborate across functions to uphold highquality standards and ensure clinical trials are executed efficiently with a patientcentric approach. The position requires to be onsite in Eysins for [. .. ] 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 [. .. ] range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress Apply now and become a part of a team that is dedicated to Sparking [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
Associate Director, Trial Clinical Delivery Lead (all genders)
• Eysins, Waadt
Führungs-/ Leitungspositionen
[. .. ] the clinical trials under your responsibility by driving innovative, valueadding solutions and ensuring the adoption of cuttingedge methodologies. Additionally, you will be responsible for developing and executing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] effective site and patient engagement strategies to secure timely recruitment and retention, ensuring ontime study delivery and successful trial outcomes. As part of our global team, youll collaborate across functions to uphold highquality standards and ensure clinical trials are executed efficiently with a patientcentric approach. The position requires to be onsite in Eysins for [. .. ] 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. 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 Clinical Operations of [. .. ] range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress Apply now and become a part of a team that is dedicated to Sparking [. .. ]
Job am 19.02.2026 bei Neuvoo gefunden
Massive Bio, Inc.
About Massive Bio Every cancer
patient deserves
access to treatment options. Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access clinical trials by eliminating [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the barriers of geography, financial constraints, and information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact [. .. ] leading pharmaceutical companies, contract research organizations (CROs) , and healthcare systems to accelerate drug development and expand equitable access to cutting-edge therapies. About the Role As the Patient Relations Coordinator, you will support cancer patients and caregivers in Germany through structured, compliant communication and coordination. You ll manage patient onboarding, documentation, and follow-ups in our systems while protecting sensitive data under GDPR standards. This role will be engaged as an independent contractor in Germany (self-employed) . Key Responsibilities [. .. ]
Job am 27.01.2026 bei Neuvoo gefunden
French Consulting
• Spangdahlem, Rhineland- Palatinate
We are looking for people who want to join our Team in Spangdahlem, Germany Apply Now JOB OPENING Title: Special Needs Identification and Assignment
Coordinator (SNIAC) Location: Spangdahlem Air [...]
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[...] Base Start Date: March 2026 Job-Type: Full Time SUMMARY The Special Needs Identification and Assignment Coordinator performs administrative duties concerning coordinating, processing, reviewing, and maintaining medical records and information pertaining to individuals and families assigned to this installation or preparing to serve in overseas assignments [. .. ] Sergeant, commanders, military and civilian agencies, AFPC, and SNIAC and command personnel worldwide to ensure proper identification of special needs families and delivery of EFMP/ SNIAC services Advocates for the patient and family/ caregivers to ensure identified education and appropriate, timely care coordination is received Conducts screening interviews with SNIAC clients to determine the need for enrollment, resources and services Schedules appointments for FMRCs and command sponsorship and ensures availability of all pertinent documentation for the appointments Uses varied and advanced [. .. ] last 24 month Applicable for both: Maintain competency in Basic Life Support (BLS) certification Have basic computer skills and working knowledge of Microsoft Office products such as Word, Excel, and Access For more information, go to our website. Upload your resume directly at https:/ / french-consulting. com/careers. French Consulting has been designated a Military Friendly Employer--French Consulting is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment [. .. ]
Job am 10.01.2026 bei Neuvoo gefunden
IQVIA
• Erfurt, Thuringia
Teilzeit
Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen Clinical Research
Coordinator/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Study Nurse (m/w/d) zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Erfurt. Diese Teilzeit-Position ist ab sofort zu besetzen, zunächst befristet auf ein Jahr. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal Investigators Sicherstellung des Wohlergehens der Patient Innen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten Qualität Betreuung der Patient Innen und Unterstützung des Personals bei administrativen Aufgaben Pflege von Studienprotokollen, Fallberichtsformularen (CRFs) , elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten Stand Planung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem Studienprotokoll Durchführung [. .. ] über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und Studienpläne Ausgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und Word Ausgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegen Sehr gute Deutschkenntnisse in Wort und Schrift #LI-CES #LI-XS #LI-HCPN #LI-DNI IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence [. .. ]
Job am 29.11.2025 bei Neuvoo gefunden
IQVIA
• Koblenz, Rhineland- Palatinate
Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen Clinical Research
Coordinator/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Study Nurse (m/w/d) zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Neuwied. Diese Position ist ab sofort zu besetzen, zunächst befristet auf 6 Monate. Der Umfang beträgt 24 Stunden pro Woche. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal Investigators Sicherstellung des Wohlergehens der Patient Innen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten Qualität Betreuung der Patient Innen und Unterstützung des Personals bei administrativen Aufgaben Pflege von Studienprotokollen, Fallberichtsformularen (CRFs) , elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten Stand Planung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem Studienprotokoll Durchführung [. .. ] über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und Studienpläne Ausgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und Word Ausgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegen Sehr gute Deutschkenntnisse in Wort und Schrift #LI-CES #LI-XB1 #LI-HCPN #LI-DNI IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Patient Access Coordinator pro Jahr?
Als Patient Access Coordinator verdient man zwischen EUR 30.000,- bis EUR 45.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Patient Access Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 8 offene Stellenanzeigen für Patient Access Coordinator Jobs.
In welchen Bundesländern werden die meisten Patient Access Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Patient Access Coordinator Jobs werden derzeit in Brandenburg (1 Jobs), Rheinland-Pfalz (1 Jobs) und Berlin (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Patient Access Coordinator Jobs?
Patient Access Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
