Role Description Als Studienärztin / Studienarzt (m/w/d) unterstützt du die Durchführung klinischer Evaluationsstudien zur Validierung digitaler Gesundheitsanwendungen. Du arbeitest eng mit unserem interdisziplinären Sidekick-Team zusammen. Dein Fokus liegt insbesondere auf der medizinischen Vorprüfung, dem Screening und der Begleitung potenzieller Studienteilnehmer:innen. Du trägst damit entscheidend dazu bei, dass unsere Studien sorgfältig, patient:innenzentriert und in Übereinstimmung mit dem Studienprotokoll durchgeführt werden. - Vorprüfung der Vorauswahl und Screening potenzieller Studienteilnehmer:innen, um die Eignung gemäß Studienprotokoll sicherzustellen - Begleitung der Randomisierung, Planung elektronischer Fragebögen sowie Verwaltung studienbezogener administrativer Aufgaben - Enge Zusammenarbeit mit dem interdisziplinären Sidekick-Team, insbesondere mit Clinical, Research und Product - Regelmäßige Abstimmung mit dem leitenden Studienarzt / der leitenden Studienärztin bzw. Principal Investigator, um den Studienfortschritt in Übereinstimmung mit dem Studienprotokoll sicherzustellen - Sicherstellung hoher klinischer und wissenschaftlicher Standards während des gesamten Studienprozesses Qualifications - Abgeschlossenes Medizinstudium mit relevanter klinischer Erfahrung als Ärztin / Arzt - Erfahrung in der Durchführung klinischer Studien von Vorteil - Patientenzentrierte, empathische Kommunikation - Starke organisatorische Fähigkeiten und eine sehr sorgfältige Arbeitsweise - Hervorragende Kommunikationsfähigkeiten mit einer teamorientierten Einstellung - Leidenschaft für digitale Gesundheitslösungen - Hohes Engagement, ausgeprägte emotionale Intelligenz und Anpassungsfähigkeit an ein dynamisches Arbeitsumfeld Benefits - Eine sinnstiftende Tätigkeit an der Schnittstelle von Medizin, Forschung und digitaler Versorgung - Mitarbeit an Evaluationsstudien für digitale Gesundheitsanwendungen mit realem Versorgungskontext - Ein interdisziplinäres, engagiertes Team mit medizinischer, wissenschaftlicher und digitaler Expertise - Flexible Zusammenarbeit in Teilzeit - Remote-Arbeit innerhalb Deutschlands oder Zusammenarbeit am Standort Hamburg - Eine projektbefristete Tätigkeit für ca. 4–6 Monate - Die Möglichkeit, aktiv zur Weiterentwicklung evidenzbasierter digitaler Gesundheitsversorgung beizutragen Contact Information Frau Jeanine Metaschk

Title: FFS Clinical Supervisor Location: Bronx NY Job Description: Ready for a summer schedule that works for you? Summer Fun Fridays at Northeast Family Services! We close at 12:30pm every Friday from Memorial Day through Labor Day — giving our team more time to relax, recharge, and enjoy the summer sunshine! Northeast Family Services is a premier mental health provider with over 20 years of experience providing services to children, youth, and families. Are you excited to join an agency with a long-standing history of providing high quality care? Well, we are excited to meet YOU! We are seeking an experienced clinician (LCSW) with supervisory experience to join our growing New York team as a Fee-For-Service Clinical Supervisor! The Fee-For-Service Clinical Supervisor will provide clinical and administrative supervision for our Home and Community Based services staff who provide structured, consistent, strength-based therapeutic interventions in a client’s home for the purpose of treating a youth’s behavioral health needs. We utilize multiple evidence-based practices that promote a family’s strengths! The Clinical Supervisor will be responsible for managing the direct care of staff, as well as overseeing the content and implementation of in-home treatment plans. The Fee-For-Service Clinical Supervisor will also carry a small caseload. If you're looking to make a change, don't miss this career opportunity to join a growing and supportive community organization that truly cares about their clients! Hybrid work schedule available Language Differential provided for Spanish, Chinese, Korean, Russian and Hindi! Qualifications: - Master's degree in social work - LCSW - Independent NY state licensure is required for this role - Minimum 2 years of experience supervising clinicians who work with children, youth, adolescents, and families in a home or community setting - Proficient with supervision, service delivery and case management fundamentals - Experience in quality management preferred - Excellent written and verbal communication skills - Proficiency with computers, including Microsoft Office - Valid driver’s license with access to a reliable vehicle preferred - Access to a laptop or CPS, secure internet, and a phone required. - Applicants must be authorized to work in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. Essential Functions: - Completing Intake Assessments - Supporting new staff through the orientation process by modeling and coaching - Completing and reviewing Treatment Plans within the Electronic Health Record - Providing weekly clinical and task supervision to staff team members - Modeling the process of opening new cases including initial home visit - Carry a small caseload of at least 10 hours per week Compensation: - $62 -$70 / Hour

Title: Oncology Clinical Research Associate (CRA) Location: United States 169069 Job Category: Job Location: Remote Security Clearance: None Business Unit: Piper Companies Division: Piper Clinical Solutions Position Owner: Anne Green Job Description: Piper Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s team. This opportunity is with an industry-leading Oncology Clinical Research organization supporting one of the top pharmaceutical companies in the world. The Oncology CRA will play a critical role in monitoring and managing clinical trials, ensuring compliance with regulatory requirements, and maintaining high standards of data integrity and patient safety. Locations for the Clinical Research Associate: Wisconsin, Michigan, Illinois, Indiana, Ohio, Oklahoma, Nebraska, Utah, Colorado, New York and Massachusetts Responsibilities for the Oncology Clinical Research Associate: - Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. - Conduct site visits, including pre-study, initiation, monitoring, and close-out visits. - Review and verify case report forms (CRFs) and source documents for accuracy and completeness. - Ensure timely and accurate reporting of adverse events and protocol deviations. - Provide training and support to site staff on study protocols, procedures, and regulatory requirements. - Maintain effective communication with study sites, investigators, and other stakeholders. - Assist in the preparation and review of study-related documentation, including informed consent forms, study manuals, and monitoring plans. - Participate in study team meetings and provide updates on site status and study progress. Qualifications for the Oncology Clinical Research Associate: - At least 3 years of experience as an On-site CRA. - Comfortable with up to 70% travel (2-3 days per week). - Must have a valid driver’s license. - Must be comfortable handling questions regarding RECIST (Response Evaluation Criteria in Solid Tumors) and CTCAE (Common Terminology Criteria for Adverse Events). - Strong understanding of clinical trial processes and regulatory requirements. - Excellent organizational and time management skills. - Strong communication and interpersonal skills. - Ability to work independently and as part of a team. - Bachelor’s degree in a related field (e.g., life sciences, nursing, pharmacy). Compensation/Benefits for the Oncology Clinical Research Associate: - Salary: $120,000 - $135,000 - Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

• Coordinates, oversees and completes functions on assigned trials activities • Performs department, Internal, Country and Investigator file reviews • Ensures tasks are performed on time, within budget and to a high quality standard • Supports study specific documentation maintenance and global support with specific systems • Provides system support (i.e. GoBalto & eTMF) • Supports scheduling and organization of client and internal meetings • Reviews and tracks local regulatory documents • Analyzes and reconciles study metrics