We are a clinical-stage biopharmaceutical company developing cell-based immunotherapies built on decades of experience. Do you want to contribute to the advancement of the next generation immune primers and relapse vaccinations? We’re assembling a team of highly motivated and skilled people who want to make a difference. We invest in talent and value diversity, join our team of professionals dedicated to improving the lives of patients with severe diseases.

Join our team: open positions

Job Title Location Date Posted
Clinical Operations Manager 14-10-2021

Are you a passionate Clinical Project Leader with oncology experience? Can you envision using your expertise to impact patients’ lives? Join our Clinical Operation team to make a purposeful difference! At Immunicum we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. You have good knowledge of project management and have excellent communication skills and fluent in English. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development. You will be responsible for the management of clinical study project(s) and report to the Head of Clinical Operations.

We are now looking for a dedicated Clinical Study Manager that will have these responsibilities:

  • Managing and leading all aspects of clinical study projects from study planning to close-out and study report,
  • Selection and oversight of performance of Clinical Research Organizations (CROs) and other vendors,
  • Oversight and regular reporting of study progress to ensure successful completion within agreed timelines/ milestones and budget,
  • Study site selection and performance and participation in site visits, as applicable
  • Participate in establishing, monitoring, and maintaining procedures (SOPs) to ensure program meets all ICH/GCP Guidelines and is Inspection Ready,
  • Contribute to building a network of hospitals, clinical experts and investigators to conduct clinical trials,
  • Organizing and participating in internal and external meetings as required,
  • Co-development and review of study documents e.g., study protocol, informed consent form, monitoring guidelines, study manuals, Case Report Forms, regulatory authority submissions,
  • Routinely review of study data and progress of EDC entry; working with data management and clinical sites to resolve data discrepancies


  • Early- Mid-phase global clinical development experience (phase I-III)
  • CRO selection & management experience
  • 5+ years in clinical project/trial management
  • Experience in oncology, preferably with immunotherapy and cell therapy
  • Degree in pharma, life-science or health related studies
  • Vendor oversight experience
  • Deep knowledge about ICH-GCP and other relevant regulation to conduct clinical trials,
  • Knowledge of IND/CTA submission to FDA and other competent authorities,
  • Experience of contract and budget negotiations with CROs, vendors and sites,
  • Proficient in MS Word, Excel and Power Point

As a person, you have an analytical mindset and maintains a high ethical standard. You are a positive, result-driven, team-oriented, agile individual with the ability to influence outcomes. Excellent organizational, communication and time management skills needed to manage multiple ongoing activities simultaneously. This position can be placed in Stockholm or Gothenburg in Sweden or in Leiden, the Netherlands.

For questions regarding the position, please contact the company’s Head of Clinical Operations Petra Domeij via email: or mobile: +46 73 354 22 06. If any questions regarding the recruitment process comes up or if you want to send in your application, please contact HR manager Zina Andersson email: or mobile: +46 735 290 109.