Clinical Manager

placeIsfya, Haifa area

Check-Cap is a clinical-stage medical diagnostics company developing C-Scan®, the first capsule-based system for preparation-free, colorectal cancer screening. Utilizing innovative ultra-low dose X-ray and wireless communication technologies, our capsule generates information on the contours of the inside of the colon as it passes naturally. This information is used to create a 3D map of the colon, which allows physicians to look for polyps and other abnormalities. Designed to improve the patient experience and increase the willingness of individuals to participate in recommended colorectal cancer screening, C-Scan® removes many frequently-cited barriers, such as laxative bowel preparation, invasiveness, and sedation.

If you are passionate about the electronic design of medical devices which will influence millions throughout the world, we are offering a unique and great opportunity for talented people, to help us build and ensure our products meet the highest standards.

We are looking for a Clinical Manager to join our company.

Responsibilities & Authorities:

  1. Full support to R&D with regards to medical devices processes, including:
    1. Planning and execution of ex-vivo, in-vivo and clinical trials
    2. Clinical application requirements (feedback to R&D on hardware, software, ergonomics etc.)
    3. Procedure’s protocol establishment
    4. Risk management process
  2. Full support of Regulatory / Clinical Strategy, including
    1. Preparation and establishment of clinical knowledge, scientific documentation such as clinical evaluation reports
    2. Development and execution of Post-marketing clinical plans
  3. Planning and execution of clinical trials according to GCP and following company SOPs including:
    1. Contract negotiation with sites
    2. Maintaining and improving relationships with physicians/investigators
    3. Preparation of trial related documentation
    4. Organizing Ethics committee submissions
    5. Performing study initiation’s visits, site monitoring and training and study termination visit
    6. Data collection, analysis and reporting
    7. Collaborating with physicians towards publication of study results
  4. Scientific and strategic evaluation of ISTs, request from grants, etc.
  5. Supporting physicians with publications, and presentations
  6. Active participation in scientific meetings / lectures / congresses
  7. Support marketing activities from the scientific/clinical point of view in strategic thinking, planning and execution
  8. In house and abroad training as requested by VP
  9. Writing clinical SOP’s
  10. Special Projects Management

Qualified candidates must meet the following requirements:

  • At least in a relevant field (Biology, medical science, bio-engineering etc.); PhD is an advantage!
  • At least 3 years’ experience of clinical affairs management, in a medical device related company
  • Should be familiar with the main clinical guidelines such as the GCP and the clinical ISO standards
  • Should be able to initiate and perform a clinical study according to the required regulations
  • Should be able to write clinical documents, SOPs, forms
  • Should be able to review clinical and scientific articles
  • Fluent English. Native English speaker is an advantage!
  • Excellent communication skills.
  • Attention to detail is extremely important.
  • Flexible and has the ability to adapt quickly to changing regulations
  • Excellent organizational, analytical, project management skills
  • A team player
  • Ability to work under pressure and to meet strict deadlines
  • Knowledge of reference manager software (Mendeley/ EndNote) and Microsoft Word formatting with styles are advantages
  • Integrity, transparency and a professional approach to work, tact and diplomacy



Employment type:

Full time

Job functions:

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