Wir stellen uns vor. Knapp 10 Köpfe, durchdachte Abläufe und der Anspruch, Mandanten bestens zu betreuen - das ist die Kanzlei Andreas Gleixner. Seit über 20 Jahren stehen wir für praxisnahe und persönliche Steuerberatung, die weit über die Deklaration hinausgeht. Mit einer guten Mischung aus Bodenständigkeit und digitaler Effizienz schaffen wir Abläufe, die nicht nur unsere Mandanten bestmöglich unterstützen, sondern auch unseren Mitarbeitern den Freiraum bieten, sich individuell weiterzuentwickeln. Was uns besonders macht? Wir kombinieren die Vorteile einer kleineren, familiären Kanzlei, in welcher Vertrauen und kurze Wege zählen, mit den spannenden Herausforderungen, die vielseitige und teils internationale Mandate bieten. Denn für uns zählt: Eine gute Zusammenarbeit führt zum Erfolg. Aufgaben Vielseitig und individuell. Freuen Sie sich auf ein abwechslungsreiches Aufgabengebiet, das wir gemeinsam nach Ihren Stärken und Interessen gestalten. Wir sind überzeugt, dass echte und langfristige Zufriedenheit bei der Arbeit nur dann entsteht, wenn die Aufgaben wirklich zu einem passen. Zu Ihren möglichen Aufgaben gehören unter anderem: - Bearbeitung der laufenden Finanz- und Lohnbuchführung - Erstellung von Jahresabschlüssen, Steuererklärungen und Einnahmenüberschussrechnungen - Bearbeitung des Zahlungsverkehrs und Reportings von Konzernmandaten - Steuerliche und betriebswirtschaftliche Beratung - Weitere Themengebiete in Ihrem Interessensfokus Qualifikation Das bringen Sie mit. Als erfahrene Steuerfachkraft (Steuerfachangestellter, Steuerfachwirt, Bilanzbuchhalter m/w/d) im Homeoffice verfügen Sie über fundiertes Wissen in unserer Branche sowie über die Abläufe in einer Kanzlei. Ihre Expertise und Zuverlässigkeit machen Sie zu einer wertvollen Unterstützung für unsere Kanzlei. Weiterhin sollten Sie die folgenden Qualifikationen mitbringen: - Erfolgreich abgeschlossene Ausbildung als Steuerfachangestellter (m/w/d) oder Weiterbildung als Steuerfachwirt, Bilanzbuchhalter (m/w/d) mit vorhandener Berufserfahrung in der Steuerberatung - Interesse an der Arbeit mit modernen Arbeitsprozessen - Eigenverantwortliche und strukturierte Arbeitsweise – wir können auf Sie im Home-Office zählen Benefits Was wir Ihnen zusätzlich bieten. Wir sind der festen Überzeugung, dass gute Arbeit nur dort entsteht, wo Motivation, Unterstützung und Freiraum für individuelle Stärken aufeinandertreffen. Deshalb bieten wir Ihnen nicht nur vielseitige Aufgaben, sondern auch ein Umfeld, das sich an Ihre Bedürfnisse anpasst und persönliche sowie berufliche Entwicklung fördert. Darüber hinaus können Sie sich auf die folgenden Benefits freuen: - Attraktive Vergütung je nach Berufserfahrung zwischen 30.000 € - 55.000 € - Großzügig flexible Arbeitszeiten mit kurzfristiger Freistellung und Urlaubsplanung - Möglichkeit 100% im Home-Office zu arbeiten - Unterstützung bei Fort- und Weiterbildungen - Sachbezugsgutscheine netto 50 € pro Monat - Ihnen fehlt es an etwas? Wir können über alles sprechen Jetzt sind Sie dran. Haben wir Ihr Interesse geweckt? Dann freuen wir uns auf Ihre Bewerbung! Ein Anschreiben ist nicht notwendig. Sie haben noch Fragen? Kein Problem! Melden Sie sich gerne telefonisch oder per E-Mail – wir nehmen uns die Zeit für ein persönliches Gespräch. Ihr Ansprechpartner Andreas Gleixner +49 (0) 8441 / 40 38 0

• Maintaining accurate financial records using Xero • Processing accounts payable and receivable, including raising and chasing invoices • Reconciling bank accounts, credit cards, and other balance sheet items on a regular basis • Preparing and submitting VAT returns in line with HMRC requirements • Managing payroll processing or liaising with an external payroll provider • Supporting month-end close procedures and producing management reports • Maintaining an organised and audit-ready filing system for financial documents • Liaising with our external accountant as required • Identifying and flagging any financial discrepancies or process improvements • Updating financial models e.g. Cash Flow, to ensure reporting is accurate

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix. What You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings • resolution. Investigates and follows-up on findings as applicable. • Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. • Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. • Provides trial status tracking and progress update reports to the team as required. Ensures study systems are complete, accurate and updated per agreed study conventions (e.g. Clinical Trial Management System). • Facilitates effective communication between investigative sites, the client company and internal project teams through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections. • Maintains and completes administrative tasks such as expense reports and timesheets in a timely manner. • Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required. Education and Experience Requirements: • Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. • Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered. • Valid driver's license where applicable. In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: • Basic medical/therapeutic area knowledge and understanding of medical terminology • Ability to attain and maintain a working knowledge of ICH GCPs and applicable regulations and procedural documents • Good oral and written communication skills, with the ability to communicate effectively with medical personnel • Good interpersonal skills • Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues • Good organizational and time management skills • Ability to remain flexibile and adaptable in a wide range of scenarios • Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving • Ability to manage Risk Based Monitoring concepts and processes • Ability to work in a team or independently as required • Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software • Good English language and grammar skills Working Conditions and Environment: • Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment. • Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays. • Exposure to biological fluids with potential exposure to infectious organisms. • Personal protective equipment required such as protective eyewear, garments and gloves. • Exposure to fluctuating and/or extreme temperatures on rare occasions.

Role Description We are seeking a detail-oriented individual to support our financial operations at Blue Whale Lending LLC. This position plays a crucial role in maintaining accurate financial records and ensuring the smooth functioning of our bookkeeping processes. - Assist in maintaining financial records and ledgers. - Process invoices and manage accounts payable. - Conduct bank reconciliations and ensure accuracy of financial statements. - Support month-end closing procedures and prepare financial reports. - Communicate with clients and vendors regarding financial transactions. - Assist with audits and provide necessary documentation. Qualifications - Proven experience in a bookkeeping or accounting role. - Strong understanding of accounting principles and practices. - Proficiency in accounting software and Microsoft Excel. - Excellent attention to detail and organisational skills. - Strong communication and interpersonal abilities.