Gehaltsübersicht für Oncology in Basel-Stadt

Leading, planning, and delivering clinical trials Phase III in Oncology & / or Infectious disease , to ensure that studies are carried out according to protocols, SOPs, regulations and principles of GCP. From start-up to close out.Lead the cross functional study team dedicated to the clinical study to ensure clinical program goals and timelines are metManage operational aspects of projects including budgeting, study initiation and risk managementSelect and manage external vendors, such as CROs, central laboratories ...Ensure the delivery of the clinical study according to ICH GCPProvide operational & scientific input into Protocol synopsis, Study protocol and all other study related documentsParticipate to due diligence activitiesYour profileMSc or PhD degree in Biotechnology, Biology, Microbiology or Life Sciences related mattersMin of 8-10+ years' experience with proven track record of international clinical trials management (Phase III) in the Pharmaceutical Industry, biotech & / or CRO. Previous monitoring experience requiredSuccessful candidate must provide sound experience in Phase III clinical trial in Oncology (& / or Haematology & / or Infectious disease): mandatorySound expertise in the implementation and use of EDC, IWRS, eTMF, CTMS and any other digital clinical trial systems.Excellent experience in management of CROs, vendors and consultantsProven track record in project management skills & team resources allocation and coordinationFluent in English Only the profiles matching the requirements will be considered (#PHASE III ONCOLOGY). Successful candidate must provide a FULL DOSSIER IN ENGLISH

 As a Portfolio Pathologist, you are part of the Digital Pathology team. You are responsible for developing the tissue biomarker strategy across several Oncology projects. You are an expert on tumor tissue analysis and Digital Pathology approaches. You generate key insights from tissue data to support drug development decision making. Responsibilities:Member of a cross-functional Digital Pathology team to be at the forefront of tissue biomarker research for OncologyProvide expertise on analysis of tumor tissue and its application to Drug DevelopmentDrive key biomarker and pathology capabilities across the Discovery and Early Clinical Development Oncology pipelineDevelop a deep expertise through study analysis and thorough knowledge of literatureGuide and challenge the use of tissue biomarkers Must haves:Medical Doctor - this is a must haveBoard certification in pathology Digital pathology and image analysis experienceExperience in tissue biomarkers such as discovering/developing insights from the analysis of tumors and tissues into testable clinical hypotheses Experience in supervising, exploring, developing and analyzing tissue analysis techniques such as immuno-histochemistry, multiplex immuno-fluorescence, image analysis and spatial-omics approachesExperience and interest in developing cutting-edge digital pathology approaches are required.   

Medical Science Liaison – Team Build – Oncology Immunotherapy As part of an exciting immuno-oncology team build across the EU comprising commercial and medical heads, IQVIA’s international medical affairs team is recruiting for 6 newly created MSL positions – based in Belgium, Portugal, Sweden, Denmark, Switzerland and Austria. Our client is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases; their therapy areas of focus include rare diseases, infectious diseases, haematological conditions, and various cancers. This oncology focused MSL team will be responsible for providing field based medical affairs support on a national level to HCPs, and local commercial colleagues, as the company expands into new European markets; working with an EMA approved, PD-1 immune checkpoint inhibitor currently indicated in cutaneous squamous cell carcinoma (CSCC), basal cell carcinoma (BCC) and non-small cell lung cancer (NSCLC) – with new indications undergoing clinical development and other exciting oncology assets in the pipeline at phase III - this is an exciting time to join an ambitious, growing company. Requirements: We are looking for candidates with very specific skills and profile: Must already be working in a similar pharma industry MSL post in the country in question Deep oncology therapy area knowledge essential, ideally within immunotherapy, melanoma, or lung cancer Prior experience of working with prelaunch products would be advantageous Outstanding communication and engagement skills Strong scientific background – ideally PhD, PharmD, MD or MSc Eligible to work in this country full time Fluency in local language and English are essential Willingness to travel nationally as required Full driving license. Benefits: Excellent salary, bonus, and benefits package We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity, and intellectual courage every step of the way. Learn more at jobs.iqvia.com . IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.Über das Unternehmen:iqvia

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: The Scientific Director, Solid Tumors, Medical Affairs will support BeiGene Clinical and Medical assets by successful execution of medical affairs programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. The candidate will report to the VP Global Medical Affairs – Solid Tumors. The Scientific Director in Medical Affairs is responsible for actively participating in or driving pre- and post-marketing medical planning & execution of assigned medical affairs activities at BeiGene , with a focus on prelaunch and launch medical activities. This position will provide scientific and/or medical oversight by thoroughly understanding oncology / immuno-oncology and serving as a key scientific/medical resource. The Director will work in a multifunctional, matrix organization, working closely with colleagues within the medical affairs group (including field medical, medical operations, medical & product training, medical information, regional and global HEOR, publication management and bioanalytics), as well as those in research & development, commercial, access & reimbursement, and patient advocacy. He/she will also collaborate with external collaborators such as health care practitioners, research groups, payers and alliance partners. Essential Functions of the Job: Active contribution to Global Medical Affairs goals and ensures compliant execution of Global medical affairs activities. Co-develops annual Global Medical affairs Plans and oversight on development and execution of key regional or Country Medical Plans with VP of GMA medical Affairs and with Therapeutic Area Leads. Focus on pre-launch and launch related Global Medical efforts supporting regions, in particular Europe, U.S, LatAm, and MENA. Maintains deep scientific and medical knowledge of relevant therapeutic/disease areas as well as an understanding of patient & physician interactions to maintain acumen in clinical decision making. Responsible for medical affairs activities consisting of data generation, data analysis and interpretation. Plays a key role in developing evidence generation strategy and execution of Phase 3B/4 studies, including interventional and observational research. Provides strategic direction and scientific and medical support for publications and presentations as needed, working closely with Publication Manager(s). Evaluates investigator-initiated trial (IIT) applications. Review and input into publications including abstracts, posters, manuscripts Provides input and reviews of Medical Information Letters. Reviews and provides input into HEOR analyses Participates in scientific engagement with external groups in order to educate and advance scientific and medical understanding of relevant disease areas, including the management of disease, standards of patient care and roles of our assets. Develops and/or reviews medical content for congresses, symposia and advisory boards. Develop strategy for global external global medical education initiatives, as well as working on developing content, review of materials for global external medical education initiatives (company sponsored) Presents scientific/medical materials to diverse audiences (e.g., physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in meeting, advisory and/or consulting settings. Provides scientific and medical input and ensures integrity of scientific content for promotional activities and sales training. May be the lead medical reviewer in the global review committee responsible for the review and approval of promotional, educational and related materials supporting Company products, ensuring medical/scientific accuracy and fair and balanced representation. Inclusive of Promotion and Medical materials for use with outside customers. Partners with country directors in all aspects of Medical Affairs activities to ensure their successful execution of their respective country medical plans and ensures alignment with Global Medical Plans. Coordinates with Project Management to ensure synergies between regions where applicable and proper development and utilization of Global Resources. Assesses medical education needs and assists in the development of internal and external educational activities with the Medical Affairs Director of Training. Works with finance, multiple functions with Medical Affairs and Project Manager to develop and forecast project budgets for medical affairs activities for responsible assets. Provides medical training for internal staff (including field medical, medical information, commercial, and sales) on products and disease related aspects, upon request. Required Education PharmD or Ph.D. with expertise in oncology / immuno-oncology Clinical research and/or drug-development knowledge and experience in oncology / immuno-oncology, required. Required Qualifications: Phd or PharmD with 5 plus years overall experience, 3 plus years experience in the pharmaceutical industry in Medical Affairs and and 2 plus years of experience in a relevant clinical practice is required. Working knowledge of applicable Federal and State Compliance guidelines and regulations required. Experience with internal Medical Affairs & Compliance related SOPs and policies required. Global Medical Affairs Experience preferred Experience with vendor selection and management preferred. Knowledge of industry standard Medical Services expected. Product launch experience is preferred. Capabilities and Competencies: Professional presence & demeanor. Values based collaborator – respectful, accountable and collaborative. Ability to relate and work with a wide range of people to achieve results. Impactful written and verbal scientific communication. Respectful and effective influencing skills. Confident, positive attitude, enthusiastic. Appreciation of diversity and multiculturalism. Strategic and creative thinker. Ability to build working relations throughout the organization and with business partners to achieve business goals within the Americas but also across multiple global regions, when necessary. Strong time management and organizational skills. Ability to manage multiple projects in a fast-paced environment. Skilled in multiple computer-based tools, in addition to software Ability to speak foreign language, preferred. Supervisory Responsibilities: N/A BeiGene Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. BeiGene is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. Currently employees are located in APAC, Americas, and Europe. BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer. BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients. For more information, see www.beigene.com. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. At BeiGene, how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things. Patients First Bold Ingenuity Collaborative Spirit Driving ExcellenceÜber das Unternehmen:BeiGene Switzerland GmbH

Category Manager (m/f/d) 100% CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2’600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives. Our network in Europe and the US offers flexible and specialized solutions across five technology platforms: Peptides, Lipids & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients. At the earliest possible date we are looking for a Category Manager (m/f/d) 100%Basel, Switzerland Basel Q3 2024 Full-time Permanent Main activities and responsibilities CordenPharma is looking for experienced Category Managers who would like to join our talent pool for future projects in order to complete the Global Category Team in the following areas: CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, Energy. In this role, you would be part of the future Global Procurement team supporting the business objectives in procurement of goods and services for the Corden Pharma group. You will represent your category across the individual Corden sites and, as such, build a crucial link between global and site Procurement. Responsible for developing and executing category strategies, conducting market analyses and research, managing relationships with key suppliers, and supporting contract negotiation and execution as required. Your primary objective is to secure the delivery of projects, goods and services across the category, thus effectively managing Corden’s Supply Chain risk. You will achieve the best value solutions for the Corden Pharma group through effective communication, and collaboration across internal departments, and by maintaining strong relationships with suppliers. Your Profile Degree or Business Administration Ability to lead cross-functional and global team Category Management experience in any of the areas; CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, is a desired Commercial strategic sourcing experience (ideally with a multi-national, Fortune 500 business) including demonstrated proficiency in contract negotiations, supplier development, and global sourcing Professional Purchasing Qualification Strong external and internal communication skills Influencing, negotiation and project management skills Experience in the pharmaceutical (especially CDMO) or chemical industry Excellent knowledge of SAP Excellent computer-based skills, including proficiency in Microsoft Office Strong proficiency in Business English What we offer 30 days of vacation Dynamic and exciting work environment Retirement Pension Plan Flexible Working Hours Interested? Your contact person Brandt, Raphael

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. The Director of Patient Advocacy and Policy, Europe, will develop and implement the patient advocacy and government affairs plan for BeiGene Europe, in alignment with the company’s purpose, mission, and priorities in the advancement of cancer care. The Director of Patient Advocacy and Policy, Europe leads how BeiGene engages with patients and patient organizations across our brand teams and our above brand activities. The role acts as a central subject matter expert, the owner of BeiGene’s patient-first strategy and a central point of contact for all patient engagement activities that are not clinical trial related. The successful candidate will be able to create insight-driven strategic plans in collaboration with cross-functional peers, and by partnering closely with global and regional corporate affairs as well as with the Medical Affairs Early Patient Engagement Team. This role is part of the Corporate Affairs team, reporting directly to the Head of Communications and External Affairs, Europe. The position is ideally based in Switzerland and would require traveling on a project basis. Essential Functions of the Job and Scope of responsibilities: Patient Advocacy Develop and implement an annual strategic advocacy and policy plan in alignment with the company’s priorities. Build and manage relationships with European advocacy organizations and patient groups as well as public health policy makers in key therapeutic areas (hematology/oncology) to fulfil mutual goals. Responsible for the design, coordination and implementation of patient community activities Identify and package campaignable information on disease and patient experience. Contribute to the development of BeiGene’s patient support materials led by medical and commercial to impact the patient journey. Drive the gathering of patient insights and perspectives that can inform internal and external communication campaigns and activities. Plan and lead patient organization engagement, including activities at major congresses in collaboration with the Medical Affairs Early Patient Engagement Team. Represent BeiGene at advocacy organizations, patient groups, policy events and scientific meetings as well as proactive outreach to organizations with shared priorities and values. Ensure the patient voice is heard internally supporting BeiGene’s patient-first culture. Partner with the BeiGene Europe Corporate Affairs team to make sure strategies and plans are integrated across Corporate Affairs disciplines, Communications, Patient Advocacy, and Government Affairs. Key contributor with stakeholders across relevant partners – Corporate Affairs, Commercial, Medical Affairs, Market Access and others. Policy Identify BeiGene’s priorities and objectives in terms of policy at the EU level; formalize and share with senior leaders. Identify and collaborate with Patient organizations at EU level (incl. in Brussels) to build common advocacy platforms in line with BeiGene’s patient policy priorities. Monitor, assess, and contribute to shape external European policy on key policy topics to address risks and opportunities. Provide political analysis of trends in relevant areas and impact on BeiGene, and advise senior leaders on policy and regional issues. Prepare regular updates on the Company’s EU patient and policy efforts for presentation to senior leaders. Qualifications: Bachelor’s degree. Biopharmaceutical industry and/or healthcare industry experience required (understanding of Hematology/Oncology space a plus) \"At least 10 years of patient advocacy /policy experience in healthcare, with at least three years in a corporate (pharma or biotech) setting. Deep experience in patient engagement campaign development, including integrated communications strategies to support disease awareness and patient access to innovation. Ability to build and maintain close, collaborative relationships with external stakeholders, including, but not limited to: patient advocacy organizations, trade associations, and policymakers. Ability to work cross-functionally across teams to build consensus around key priorities. ability to lead cross-function patient advocacy and policy-related work streams. Knowledge of regulatory, access, and reimbursement policies in the European setting, at European Union (EU) level, but also including non-EU and former member states. Understanding of the European Parliament, including and not limited to key issues including intellectual property, labor, taxes, and trade and other issues specific to Hematology/Oncology Skills and Abilities: Excellent English writing skills Proven relationship development and management skills. Strong cross-functional matrix management and leadership skills to foster a culture of collaboration. Works well in a fast-paced environment. Strong oral communication skills and ability to convey complex issues to a variety of audiences. Detail-oriented, with a strong ability to organize and analyze. Ability to work independently and use sound judgment in decision-making, including setting and managing priorities and meeting competing deadlines. Possesses sound judgment, critical thinking, and decision-making skills. Influences with and without authority; can effectively make a case for and follow through on strategic and tactical recommendations. High ethical standards and an appreciation of compliance requirements. Collaborative, self-directed team player. #LI-Remote BeiGene Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. BeiGene is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. Currently employees are located in APAC, Americas, and Europe. BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer. BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients. For more information, see www.beigene.com. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. At BeiGene, how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things. Patients First Bold Ingenuity Collaborative Spirit Driving ExcellenceÜber das Unternehmen:BeiGene Switzerland GmbH

Die Abteilung für pädiatrische Hämatologie und Onkologie sucht eine/-nClinical Research Coordinator (CRC) (Studiendokumentar/in) 70%Der Einsatz erfolgt im Rahmen des Forschungsverbunds SPOG (Swiss Pediatric Oncology Group). Die SPOG ist der nationale Verein zur Durchführung klinischer Studien für onkologisch / hämatologisch erkrankte Kinder in der Schweiz. Dadurch sollen alle an Krebs erkrankten Kinder und Jugendlichen Zugang zu passenden Behandlungsoptionen kommen. Werden Sie Teil dieses Netzwerks!Hauptaufgaben:Koordinative Aufgaben im Rahmen des Forschungsverbunds SPOG für das UKBB Unterstützung der Prüfärztinnen und -ärzte bei der Durchführung von klinischen Studien und wissenschaftlichen Projekten Organisation und Durchführung von Visiten der Studienpatienten/Innen Vorbereitung und Organisation von Studien spezifischen Materialien und Proben einschließlich derer Versand Assistenz bei Protokoll-/ GCP-konformer Durchführung von Studien Erfassung und Meldung von AEs, SAEs und SUSARs Erhebung und Dokumentation von Therapieverläufen und Follow-up's in CRFs mittels diverser Datenbanken sowie Aktualisierung und Archivierung von Studiendokumenten Vorbereitung und Begleitung von Monitoring-Visiten, Audits und Inspektionen Anforderungen:Abgeschlossene Ausbildung als Clinical Research Coordinator (CAS) oder als Pflegefachperson/Study Nurse oder Abschluss in einem medizinischen Assistenzberuf Erfahrung in der Durchführung und Organisation von klinischen Studien nach ICH-GCP von Vorteil Forschungserfahrung in einem Team von Studienkoordinatorinnen und -koordinatoren von Vorteil Begeisterung für die Thematik Ein hohes Maß an Qualitätsbewusstsein, Organisationsfähigkeit sowie eine selbständige und strukturierte Arbeitsweise Sehr gute Team- und Kommunikationsfähigkeit fundierte Computerkenntnisse der gängigen MS-Office Anwendungen und Datenbankprogramme Kenntnisse der med. Terminologie Gute Deutsch- und Englischkenntnisse in Wort und Schrift Wir bieten:Eine innovative, interessante und abwechslungsreiche Tätigkeit in einem kleinen, freundlichen und hoch motivierten interdisziplinären Team Regionale und überregionale Zusammenarbeit und Austausch mit KollegInnen Gute Weiterbildungsmöglichkeiten in unserem Netzwerk (SPOG) und an der CTU der Universität Basel Gute Berufsaussichten in einer zukunftssicheren Branche Bewerbungsfrist: 29. Februar 2024Richten Sie Ihre Bewerbung bitte an:Universitätskinderspital beider Basel UKBBAbteilung für Pädiatrische Hämatologie/Onkologie Prof. Dr. med. Nicolas von der Weid, AbteilungsleiterSpitalstrasse 334031 BaselE-Mail: [email protected] freuen uns auf Ihre Online-Bewerbung!Bitte nehmen Sie sich einen kurzen Moment Zeit und füllen Sie die Felder auf der nächsten Seite aus. Halten Sie dazu Ihre vollständigen Bewerbungsunterlagen elektronisch bereit.Bei allgemeinen Fragen zur Stelle oder zum Bewerbungsprozess hilft Ihnen unser HR Team, Telefon +41 61 704 12 32 gerne weiter.Wir freuen uns auf Ihre Online-Bewerbung!Bitte nehmen Sie sich einen kurzen Moment Zeit und füllen Sie die Felder auf der nächsten Seite aus. Halten Sie dazu Ihre vollständigen Bewerbungsunterlagen elektronisch bereit.Bei allgemeinen Fragen zur Stelle oder zum Bewerbungsprozess hilft Ihnen unser HR Team, Telefon +41 61 704 12 32 gerne weiter.Universitäts-Kinderspital beider Basel Basel Unbefristet Vollzeit 5 Stunden her Bereich:Station C, Onkologie/HämatologieEintrittsdatum:01.03.2024Abteilung:Das Universitätskinderspital beider Basel (UKBB) ist ein führendes Zentrum der schweizerischen universitären Kindermedizin. Seine Abteilung für pädiatrische Hämatologie und Onkologie betreut jährlich ca. 35 neue KrebspatientInnen im Rahmen von internationalen klinischen Studien und ist eines der 5 universitären Zentren der SPOG. Schwerpunkte der Abteilung sind die Neuroonkologie, die Sarkome und die allogene Stammzelltransplantation.

Junior Treasury Analyst (m/f/d) 100% CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2’600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives. Our network in Europe and the US offers flexible and specialized solutions across five technology platforms: Peptides, Lipids & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients. At the earliest possible date we are looking for a Junior Treasury Analyst (m/f/d) 100%Basel, Switzerland Basel ASAP Full-time Permanent Main activities and responsibilities This position will play a crucial role in managing our company's liquidity, supporting the optimisation of cash flow, and mitigating financial risks. It will also support treasury accounting, as well as ad hoc projects. The Junior Treasury Analyst will work closely with various departments, financial institutions, and external partners to ensure effective treasury operations. Execute day-to-day treasury activities, including cash management, liquidity forecasting, and fund transfer Monitor cash pooling activities Monitor the intracompany loan relationships and interest calculations Oversee the management of bank accounts, ensuring optimal utilisation of cash resources Conduct cash analyses to support business decision-making Prepare reports on key liquidity metrics and performance indicators. Evaluate exposure to currency and interest rate risk Monitor regulations and industry trends to ensure compliance Perform Treasury Accounting via closing for loans and interest and audits Your Profile Bachelor's degree in Finance, Accounting, or a related field; Master's degree or professional certification is a plus Ideally 1 to 3 years proven experience in treasury operations, experience with holding companies is a plus Familiarity with international financial regulations Strong analytical and problem-solving skills Excellent communication and interpersonal skills Proficiency in treasury management systems and financial software Not afraid to speak up, creative and pro-active work style English at a very good level - other languages are a plus What we offer 30 days of vacation Retirement Pension Plan Dynamic and exciting work environment Accessible Workplace Interested? Your contact person Brandt, Raphael

Category Manager (m/f/d) 100% CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces active pharmaceutical ingredients, medicines and associated packaging services on behalf of its customers as a “full-service” service provider. The group employs around 3,000 people. Our network in Europe and the USA offers flexible and specialized solutions across five technology platforms: peptides, lipids & carbohydrates, injectables, highly potent active ingredients & oncology and small molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients. CordenPharma International (CPI) acts as the management company of the CordenPharma Group. In addition to the Executive Leadership Team, CPI has central functions such as Sales & Marketing, Legal, HR and Corporate Development, which work for the CordenPharma Group across locations and at an international level. We are looking for one as soon as possible Category Manager (m/f/d) 100%Basel, Switzerland Basel Q3 2024 Full-time Permanent Main activities and responsibilities CordenPharma is looking for experienced Category Managers who would like to join our talent pool for future projects in order to complete the Global Category Team in the following areas: CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, Energy. In this role, you would be part of the future Global Procurement team supporting the business objectives in procurement of goods and services for the Corden Pharma group. You will represent your category across the individual Corden sites and, as such, build a crucial link between global and site Procurement. Responsible for developing and executing category strategies, conducting market analyses and research, managing relationships with key suppliers, and supporting contract negotiation and execution as required. Your primary objective is to secure the delivery of projects, goods and services across the category, thus effectively managing Corden’s Supply Chain risk. You will achieve the best value solutions for the Corden Pharma group through effective communication, and collaboration across internal departments, and by maintaining strong relationships with suppliers. Your Profile Degree or Business Administration Ability to lead cross-functional and global team Category Management experience in any of the areas; CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, is a desired Commercial strategic sourcing experience (ideally with a multi-national, Fortune 500 business) including demonstrated proficiency in contract negotiations, supplier development, and global sourcing Professional Purchasing Qualification Strong external and internal communication skills Influencing, negotiation and project management skills Experience in the pharmaceutical (especially CDMO) or chemical industry Excellent knowledge of SAP Excellent computer-based skills, including proficiency in Microsoft Office Strong proficiency in Business English What we offer 30 days of vacation Dynamic and exciting work environment Retirement Pension Plan Flexible Working Hours Interested? Your contact person Brandt, Raphael

Junior Treasury Analyst (m/f/d) 100% CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces active pharmaceutical ingredients, medicines and associated packaging services on behalf of its customers as a “full-service” service provider. The group employs around 3,000 people. Our network in Europe and the USA offers flexible and specialized solutions across five technology platforms: peptides, lipids & carbohydrates, injectables, highly potent active ingredients & oncology and small molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients. CordenPharma International (CPI) acts as the management company of the CordenPharma Group. In addition to the Executive Leadership Team, CPI has central functions such as Sales & Marketing, Legal, HR and Corporate Development, which work for the CordenPharma Group across locations and at an international level. We are looking for one as soon as possible Junior Treasury Analyst (m/f/d) 100%Basel, Switzerland Basel ASAP Full-time Permanent Main activities and responsibilities This position will play a crucial role in managing our company's liquidity, supporting the optimisation of cash flow, and mitigating financial risks. It will also support treasury accounting, as well as ad hoc projects. The Junior Treasury Analyst will work closely with various departments, financial institutions, and external partners to ensure effective treasury operations. Execute day-to-day treasury activities, including cash management, liquidity forecasting, and fund transfer Monitor cash pooling activities Monitor the intracompany loan relationships and interest calculations Oversee the management of bank accounts, ensuring optimal utilisation of cash resources Conduct cash analyses to support business decision-making Prepare reports on key liquidity metrics and performance indicators. Evaluate exposure to currency and interest rate risk Monitor regulations and industry trends to ensure compliance Perform Treasury Accounting via closing for loans and interest and audits Your Profile Bachelor's degree in Finance, Accounting, or a related field; Master's degree or professional certification is a plus Ideally 1 to 3 years proven experience in treasury operations, experience with holding companies is a plus Familiarity with international financial regulations Strong analytical and problem-solving skills Excellent communication and interpersonal skills Proficiency in treasury management systems and financial software Not afraid to speak up, creative and pro-active work style English at a very good level - other languages are a plus What we offer 30 days of vacation Retirement Pension Plan Dynamic and exciting work environment Accessible Workplace Interested? Your contact person Brandt, Raphael