Careers

Our mission is to discover novel drug targets and develop innovative cancer treatments to extend the reach of immunotherapies to new patient populations. In our work, we combine cutting edge computational solutions and rigorous experimentational processes to advance our mission.

Our extraordinary multidisciplinary team brings together life sciences and data sciences expertise. It is one of our greatest assets. This merging of talent promotes diverse ways of thinking and cultivates an atmosphere of excellence, creativity and openness. Collaboration across disciplines and areas of expertise is fundamental to our work. Ensuring that all of our talented employees make the best use of their ambition, knowledge and expertise is a key driver for individuals, teams and the success of our company.

As a leading biotechnology company in computational biology and an innovator in the field of cancer immunotherapy, we are looking for life and data scientists, clinicians and healthcare professionals that share our passion for making a difference and developing new potential cancer treatments.

If you are interested in becoming a part of this exceptional team and working in a collaborative, dynamic and supportive environment, you are encouraged to send us your resume. Suitable candidates will be contacted.

Job Description

The Head of IR and Corporate Communications will be responsible for all the professional aspects that facilitate the communications and IR activities of the company including, the company’s positioning in the financial community, communications with investors and analysts, communication in the various media platforms, the corporate website and corporate presentations, manage press releases as well as overall supervision and handling of company’s marketing material. The Head of IR and Corporate Communications reports to the CFO (based in Israel) and can be located worldwide.

  • Responsibility for all investor relations aspects of the company
    • Develops and maintains the company’s investor relations plan
    • Creates presentations, press releases, quarterly scripts and other investor-related communication materials
    • Monitors analyst reports and summarizes them for senior management
    • Serves as the first point of contact for the investments community
    • Organizes conferences, road shows, earnings conference calls, and investor meetings
    • Maintenance of investor date base and targeting new investors
    • Represents the views of the investor community to the management team
  • Responsibility for all communications aspects of the company
    • Develops and maintains a company communication plan
    • Press releases
    • Company presentations – corporate and other
    • Traditional and social Media
  • Responsible for website
  • Unifying “marketing language” across the various marketing aspects
  • MarCom materials

Job Requirements

  • Academic degree in life-Science / Biology
  • Minimum 3 year in IR at a NASDAQ-traded company – a must
  • Prior experience with life science companies– a must; biotech – an advantage
  • Prior experience in generating marketing materials – a big advantage
  • English mother tongue level – a must
  • Effective communication and presentation skills
  • Highly developed senses of responsibility and organization
  • Highly independent and self-motivated
  • Hands on person

Job Description

Compugen’s extraordinary multidisciplinary team is one of its greatest assets. Our employees, coming from different backgrounds with diverse ways of thinking, work together in an atmosphere that cultivates excellence, creativity and openness. The cooperation of people from various disciplines involving different areas of expertise is fundamental to our ability to establish unique predictive drug discovery solutions, as well as to discover and develop novel therapeutic proteins and drug targets. This merging of talent from various disciplines continues to serve as a key growth driver and enables us to fulfill our mission and business goals.

  • The Sr. Software Engineer will lead the development of Compugen’s Computational Discovery analytics platform towards the in-silico identification of drug targets and novel biomarkers in immuno-oncology (IO)
  • Lead the Software Development Life Cycle (SDLC), including detail scoping, requirements gathering, hands-on architecture, design and implementation, testing, launch, maintenance, support and agile adaptation to end-users’ feedback
  • Develop and implement innovative cloud-based analytics platform of high-throughput biological data such as genomics, proteomics, imaging and clinical meta data
  • Drive back-end, front-end and API developments
  • Utilization of state-of-the-art technologies for real-time queries, analytics and visualization
  • Continuous improvement, QA/QC and cloud cost optimization
  • Apply best practice in information security and access control of the developed platform
  • Work in close collaboration with biologists, bioinformatics and data scientists, as well as with stakeholders and management across the company
  • Present, visualize and communicate the development roadmap and achieved milestones to internal and external collaborators

Job Requirements

  • B.Sc. or equivalent hands-on years of experience in Computer Science/Engineering
  • 5+ years of hands-on commercial-grade software development
  • Strong full-stack software development skills in Python, AngularJs., NodeJs, JavaScript, Django, Laravel, CSS, JQuery, REST API
  • Extensive experience in databases and data science technologies such as MySQL, PostgreSQL, MongoDB, DynamoDB, RedShift, Apache SPARK
  • Hands-on experience in cloud-based (AWS preferred) platform development with Datalakes, Dockers, Kubernetes, MapReduce, RDS
  • Best practice in code repository (Github, CodeCommit), documentation and version control, in development and production environments
  • Agile/SCRUM and Kanban development
  • Ability to propose, scope and carry out independently end-to-end software development projects
  • Demonstrated impact via the development of novel computational platforms, and the adoption of new technologies
  • Experience in the biotech and pharmaceutical industry – an advantage
  • Background in a development environment that handles large-scale datasets
  • UX experience – an advantage
  • Dev-Ops experience – an advantage
  • A team player in a multidisciplinary environment
  • Outstanding interpersonal, verbal and written communication skills
  • Strong collaborative skills, professionalism and long term commitment

Job Description

Compugen is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable, predictive computational discovery platforms to identify novel drug targets and develop first-in-class therapeutics in the field of cancer immunotherapy. Our therapeutic pipeline consists of immuno-oncology programs against novel drug targets we discovered computationally, including T cell immune checkpoints and additional early-stage immune-oncology programs focused largely on myeloid targets. As we advance our pipeline, we are looking for a candidate with expertise in clinical development safety and pharmacovigilance. The successful candidate is expected to work cross functionally within the company on multiple programs. This position reports to the Chief Medical Officer.

  • Provide leadership and direction for all safety and pharmacovigilance activities
  • Guidance and oversight of CROs and other stakeholders
  • Key job responsibilities: include signal detection, authoring safety management plan, benefit-risk assessment, risk management and mitigation and leading the development of regulatory documents with safety sections such as IB, clinical protocol, DSUR, clinical study reports, SAP, SMP

Job Requirements

  • Advanced degree in the life sciences MD, PhD
  • Three years’ experience in the pharmaceutical industry as a safety clinician in hematology, medical oncology, prior experience as a safety physician with immuno-oncology clinical trials- Advantage
  • Prior experience interacting with regulatory authorities, collaborating with and leading cross-functional teams- Advantage
  • Extensive knowledge of global safety reporting guidelines, review and interpretation of safety data in the relevant databases (safety and clinical database) and interpretation of safety data from clinical studies
  • Extensive knowledge of regulatory guidelines (GCP, ICH)
  • Demonstrated track record of success working on cross functional multidisciplinary teams
  • Relevant experience leading or supporting regulatory filing (IND, NDA, BLA), safety-related interactions with regulatory authorities
  • Contribute to safety-related discussions on candidate drugs in the pipeline
  • Excellent writing and communication skill
  • This role requires up to 20% travel

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