Role Description Für unser Team suchen wir einen Werkstudenten (m/w/d), der uns in der manuellen Auftragsbearbeitung sowie der Kommunikation mit unseren Kunden unterstützt. In dieser Position wirst du eine Schlüsselrolle bei der Koordination und dem reibungslosen Ablauf unserer Dienstleistungen spielen. Du erhältst wertvolle Einblicke in den Arbeitsalltag eines Software-Unternehmens und wirst dabei sowohl eigenständig als auch im Team arbeiten. - Kundenkommunikation: Du stehst in direktem Kontakt mit unseren Kunden über WhatsApp und hilfst bei der Angebotsannahme. - Angebotserstellung und Mailversand: Du erstellst individuell zugeschnittene Angebote und versendest diese an die Kunden. - Management von Ghostwritern und Kunden: Du verteilst Aufträge an die passenden Ghostwriter und stellst sicher, dass diese rechtzeitig bearbeitet werden. Qualifications - Studium: Du bist eingeschriebene:r Student:in, idealerweise in einem wirtschaftswissenschaftlichen, kommunikations- oder projektmanagementbezogenen Studiengang. - Kommunikationsfähigkeiten: Du bist sicher im schriftlichen und mündlichen Umgang mit Kunden und kannst dich präzise und professionell ausdrücken – besonders bei der Kommunikation über WhatsApp und per E-Mail. - Organisationstalent: Du hast ein gutes Zeitmanagement, behältst den Überblick über mehrere Aufgaben gleichzeitig und kannst Deadlines einhalten. - IT-Kenntnisse: Du hast Erfahrung im Umgang mit gängigen Bürosoftware-Anwendungen (z.B. Microsoft Office, Google Docs) und bist bereit, neue Tools wie Notion zu erlernen. - Flexibilität und Selbstständigkeit. - Erfahrung im Kundenservice oder Projektmanagement: Idealerweise hast du bereits erste Erfahrungen in der Kundenkommunikation oder Projektkoordination gesammelt, dies ist jedoch nicht zwingend erforderlich. Benefits - Eigenes Firmen-MacBook: Du erhältst ein modernes und leistungsstarkes MacBook, das du für deine Arbeit nutzt – ideal für deine Produktivität und Flexibilität. - Urban Sports: Profitiere von einer Mitgliedschaft bei Urban Sports und halte dich fit, indem du eine Vielzahl von Fitness- und Sportmöglichkeiten in deiner Stadt nutzt. - 100% Remote- oder Home Office: Arbeite von überall aus – Hauptsache deine Zeitzone passt! Du hast die Freiheit, deinen Arbeitsort flexibel zu wählen, ohne an ein Büro gebunden zu sein. Ins Büro kannst Du aber auch gerne kommen. - Flexibilität: Gestalte deine Arbeitszeiten so, dass sie zu deinem Studium und deinen anderen Verpflichtungen passen. Wir bieten dir die Freiheit, deinen Arbeitsalltag selbst zu organisieren. - Wertvolle Erfahrungen: Du sammelst praktische Erfahrungen in einem innovativen Unternehmen und erhältst Einblicke in das Projektmanagement und die Kundenkommunikation in der Welt des akademischen Ghostwritings. - Persönliche Weiterentwicklung: Du wirst Teil eines engagierten Teams und hast die Möglichkeit, dich beruflich weiterzuentwickeln und Verantwortung zu übernehmen.

Role Description Oversee the construction and renovation of Atrium’s managed properties, ensuring projects align with approved design and planning goals. - Leads the selection and management of contractors and vendors, ensuring all projects are executed efficiently, completed on time, and maintained within approved budget parameters. - Monitor project performance using systems to track budgets, schedules, and quality control standards. - Maintain organized and sustainable capital records, making warranty and pricing information easily accessible. - Coordinate each project’s construction process, ensuring input from all key stakeholders (owner, manager, department heads) to optimize guest impact and long-term value. Qualifications - 5+ years of experience in hotel sector construction – You should be a seasoned pro at managing renovation and new build projects in the hospitality industry. - In-depth knowledge of Hotel Brands – Understanding the specific needs of brands like Marriott, Hilton, and IHG ensures you’ll meet their standards every time. - Proven track record of CAPEX project execution – You’ll need to demonstrate a solid history of managing and completing capital improvement projects successfully. - Vendor insight – Your understanding of the vendor and contractor landscape in hospitality will help guide your decisions and keep projects on track. - Availability to travel up to 50% – This role requires regular travel to support projects across multiple locations. Requirements - Accountable Achiever: You take ownership and deliver results. - Agile Thinker: You adapt quickly to changing circumstances. - Talent Curator: You attract, develop, and retain top talent. - Transparent Leader: You communicate openly and honestly. - Leading with SPIRIT: You embody our core values of Service, Perseverance, Inclusion, Respect, Innovation, and Teamwork. Benefits - Career Growth & Learning – 40% of our management hires are internal promotions! - Invest in Your Future – 401(k) plan with company match. - Comprehensive Health Coverage – Medical, dental, and vision insurance options. - Paid Time Off & Vacation – Enjoy exclusive Atrium Traveler and brand discount programs to explore new destinations. - Perks That Fit Your Life – Enjoy DailyPay, wellness programs, tuition reimbursement, and exclusive discounts on your favorite brands and services. - Purpose & Impact – Make a difference through Atrium’s community service and volunteer programs.

Role Description Our client is searching for a Project Manager that has experience managing international projects for a long-term contract that may lead to full-time employment. ***All candidates must have experience managing a variety of projects that include international operations*** Duties: - Creating project plans that include tasks, milestones, and timelines - Identifying and finding solutions for potential risks, such as budget constraints or supplier delays - Selecting employees for the project team or assistant project managers, and delegating tasks - Managing the budget and allocating resources Benefits - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully remote position. Application Deadline This position is anticipated to close on Jun 22, 2026.

Role Description Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle activities for all assigned projects in alignment with the Global Regulatory Lead. Translates complex pertinent global requirements and provides an assessment of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. Works collaboratively with members of the global regulatory team to develop global regulatory plans, address global regulatory issues, health authority queries, and regulatory obligations. Job Responsibilities - Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL). - Identifies the need and obtains regulatory intelligence, researches precedent approvals and prior health authority decisions to assess applicability to support development of strategic options for assigned Otsuka products. - Translates complex pertinent global requirements and provides an assessment of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing, regulatory operations, etc.) to develop global regulatory plans, address global regulatory issues, health authority queries, and regulatory obligations. - Authors, coordinates, reviews, and executes submissions and responses to regulatory authorities related to INDs, amendments, supplements, aggregate reports, NDAs (as applicable) within company timelines and in accordance with regulations and guidelines. - Independently manages preparation of INDs, CTAs, amendments, supplements, and aggregate reports within company timelines and in accordance with regulations and guidelines. - Confirms submission documents are accurate, compliant, and high-quality to allow for smooth and expeditious approvals from regulatory authorities. - Serves as the sponsor point of contact to the health authority. - Represents GRA in project team meetings and provides regulatory guidance and perspective to the cross-functional team in conjunction with GRL, to determine appropriate actions to meet timelines and/or resolve issues. - Effectively manages and directs internal support staff and external consultants for assigned projects. - Interacts effectively with internal/external functional business units to gather data and develop documentation required for on-time submissions. - Works closely with GRA department to execute departmental initiatives to improve overall efficiency, quality, and/or output. - Assesses and develops innovative ideas to move GRA department to address current and future challenges. Qualifications - Experience working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of global regulatory submissions (IND, CTA, NDA or BLA, MAA). - RAC certification a plus. Requirements - Strong oral and written communication skills. - Solid working knowledge and understanding of the drug development process, laws, regulations, and guidelines including FDA, ICH, etc. - Able to successfully interpret and apply regulatory intelligence to work output. - Ability to lead teams, prioritize work, proactively manage and communicate issues, scopes progress and risks throughout the project lifecycle ensuring key stakeholders are informed. - Able to establish close communications and working relationships with cross-functional teams to meet business objectives. - Results-oriented, entrepreneurial, and self-motivated with excellent organizational skills with ability to learn and grow. - Strong demonstrated experience with Microsoft Office programs (Word, Excel, PowerPoint, Outlook) and familiarity with electronic document management systems (EDMS). Education and Related Experience - Bachelor's degree with 5+ years’ experience or Master’s degree with 2 years’ experience in regulatory affairs or related areas (e.g., clinical development, project management, quality assurance, etc.) in pharmaceutical or healthcare related industry. - Experience with FDA or other health authority interactions desirable. Benefits - Comprehensive medical, dental, vision, prescription drug coverage. - Company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance. - Tuition reimbursement, student loan assistance. - A generous 401(k) match. - Flexible time off, paid holidays, and paid leave programs. - Other company provided benefits.